Author: RR

Emerging Real-World Evidence Positions GLP-1 Receptor Agonists in Colorectal Cancer Prevention

RR

SUMMARY: Colorectal cancer (CRC) is the third most common cancer diagnosed in both men and women in the United States. The American Cancer Society estimates that approximately 158,850 new cases of CRC will be diagnosed in the United States in 2026 and about 55,230 patients will die of the disease. Colorectal cancer is a heterogeneous disease classified by its genetics, and even though the diagnosis of CRC in the US is dropping among people 65 years and older, the incidence has been rising in the younger age groups, with 12% of CRC cases diagnosed in people under age 50.

Background: Rethinking Chemoprevention in CRC

Colorectal cancer (CRC) remains a leading cause of cancer-related morbidity and mortality worldwide, underscoring the need for effective prevention strategies. Historically, low-dose Aspirin has been investigated for its potential chemopreventive effects, largely due to its anti-inflammatory properties. However, its clinical utility has been tempered by modest benefit and clinically significant risks, particularly gastrointestinal bleeding and ulceration. As a result, Aspirin is no longer broadly recommended for CRC prevention in average-risk populations.

In parallel, Glucagon-Like Peptide-1 Receptor Agonists (GLP-1RAs), now widely prescribed for type 2 diabetes and obesity, have emerged as potential anticancer agents. Preclinical evidence suggests these drugs may inhibit colorectal carcinogenesis through anti-inflammatory and anti-proliferative effects, including downregulation of the PI3K/Akt/mTOR signaling pathway. Despite this mechanistic rationale, real-world comparative data have been lacking, until now.

Study Design and Methods                       

A large-scale retrospective analysis leveraging the TriNetX network, encompassing data from approximately 150 million patients across 106 healthcare organizations, offers new insight into this evolving landscape. In this study, 281,656 patients were propensity score-matched to compare GLP-1RA users with Aspirin users (140,828 per cohort), balancing demographics, comorbidities, and key confounders. The cohorts were broadly similar, with a mean age of 58 years and a predominance of female participants (69%). The Primary endpoint was CRC incidence.

Key Findings

GLP-1 receptor agonists were associated with a meaningful reduction in colorectal cancer incidence compared with Aspirin.

Over a median follow-up of approximately 5.9 years for GLP-1RA users and 4.8 years for Aspirin users, GLP-1RA therapy was associated with a statistically significant reduction in CRC incidence. Specifically, CRC occurred in 0.13% of GLP-1RA users compared with 0.176% of Aspirin users, translating to a 26% relative risk reduction. These findings were consistent across sensitivity analyses at 12 and 36 months, as well as across multiple subgroups, including variations in age, BMI, and glycemic status.

Notably, the observed benefit extended to younger populations and individuals without obesity or diabetes, suggesting potential effects beyond metabolic modulation. Among individual agents, Semaglutide demonstrated a statistically significant association with reduced CRC risk, while Liraglutide and Dulaglutide also showed signals of benefit in secondary analyses.

In contrast, no significant risk reduction was observed among patients with tobacco use or established atherosclerotic disease. Tirzapeptide and Exenetide did not show the same significance in this study and these findings raise important questions regarding potential heterogeneity within the class.

Safety Profile

The safety comparison revealed distinct differences between the two cohorts. From a safety perspective, GLP-1RA use was associated with fewer serious adverse events such as gastrointestinal bleeding, stomach ulcers, and acute kidney injury compared with Aspirin. As expected, gastrointestinal symptoms, including nausea, vomiting, abdominal pain, and diarrhea, were more frequently reported with GLP-1RAs, though these were generally manageable.

Clinical Interpretation

Despite the relative risk reduction, the absolute benefit at the individual level remains modest, with a number needed to treat (NNT) of approximately 2,198 to prevent one case of CRC. However, this must be interpreted within a broader population context. With millions of individuals currently prescribed GLP-1RAs for metabolic indications, even small individual risk reductions could translate into meaningful public health impact.

This study represents the first large, real-world, head-to-head comparison of GLP-1 receptor agonists and Aspirin for primary CRC prevention. The findings underscore a potential paradigm shift, positioning GLP-1RAs as agents that may extend beyond metabolic disease management into the realm of cancer prevention.

While these results are compelling, they remain hypothesis-generating. Prospective randomized clinical trials will be essential to validate causality, clarify agent-specific effects, and define optimal patient populations. Nonetheless, the convergence of metabolic and oncologic benefits highlights an emerging opportunity to rethink prevention strategies in colorectal cancer.

Key Takeaways for Oncology Practice

  • GLP-1 receptor agonists were associated with a 26% relative reduction in CRC incidence compared with Aspirin
  • Benefits were consistent across multiple patient subgroups and timepoints
  • Semaglutide emerged as the most robust individual agent in this analysis
  • GLP-1RAs demonstrated a more favorable safety profile, particularly regarding bleeding risk
  • Absolute risk reduction is small, but population-level implications may be significant

GLP-1 receptor agonist vs aspirin for primary prevention of colorectal cancer: Evidence from a real-world head-to-head comparison. Jones C, Obomanu E, Neely A, et al. J Clin Oncol 44(suppl 2; abstr 18), 2026.

Breakthrough Results from the CARTITUDE-4 Trial: A Major Step Forward in Multiple Myeloma Treatment

RR

SUMMARY: Multiple Myeloma (MM) is a clonal disorder of plasma cells in the bone marrow and the American Cancer Society estimates that in the United States, 36,000 new cases will be diagnosed in 2026, and 10,850 patients are expected to die of the disease. Multiple Myeloma is a disease of the elderly, with a median age at diagnosis of 69 years and characterized by intrinsic clonal heterogeneity. Almost all patients eventually will relapse, and patients with a high-risk cytogenetic profile, extramedullary disease or refractory disease have the worst outcomes.

Modern therapies,including Proteasome Inhibitors, Immunomodulatory drugs, and anti-CD38 antibodies, have extended survival to nearly a decade. However, patients whose disease becomes resistant to these treatments face poor outcomes with a median survival of less than 1 year. There is a critical need for novel, effective therapies with new mechanisms of action

B-cell Maturation Antigen (BCMA) is a member of the Tumor Necrosis Factor superfamily of proteins. It is a transmembrane signaling protein primarily expressed by malignant and normal plasma cells and some mature B cells. BCMA is involved in JNK and NF-kB signaling pathways that induce B-cell development and autoimmune responses.

CAR T-Cell Therapy & BCMA Targeting

Anti-BCMA CAR T-Cell Therapy is a type of immunotherapy and consists of T cells collected from the patient’s blood in a leukapheresis procedure. These T cells are then stimulated by treating with interleukin 2 (IL-2) and anti-CD3 antibodies in vitro, so that they will actively proliferate and expand to large numbers. These T cells are then genetically engineered to produce special receptors on their surface called Chimeric Antigen Receptors (CAR), by transducing with a gene encoding the engineered CAR, via a retroviral vector such as lentiviral vector. These reprogrammed cytotoxic T cells with the Chimeric Antigen Receptors on their surface are now able to recognize a specific antigen such as BCMA on tumor cells. These genetically engineered and reprogrammed CAR T-cells are grown in the lab and are then infused into the patient. These cells in turn proliferate in the patient’s body and the engineered receptor on the cell surface help recognize and kill cancer cells that expresses that specific antigen such as BCMA. The patient undergoes lymphodepletion chemotherapy with Fludarabine and Cytoxan prior to the introduction of the engineered CAR T-cells to upregulate cytokine production and promote the expansion of the engineered CAR T-cells.

Ciltacabtagene autoleucel (Cilta-cel; CARVYKTI®), a B-cell maturation antigen (BCMA)-directed CAR T-cell therapy indicated for the treatment of patients with relapsed or refractory multiple myeloma who have received at least 1 prior line of therapy, including a proteasome inhibitor and an immunomodulatory agent, and are refractory to Lenalidomide.

 CARTITUDE-4 Study

CARTITUDE-4 is an ongoing open-label, multicenter, randomized Phase III trial conducted to compare Cilta-cel with the physician’s choice of either of two highly effective standard-of-care therapies, in patients with Lenalidomide-refractory multiple myeloma after one to three lines of therapy. In this study a total of 419 eligible patients (N=419) were randomly assigned in a 1:1 ratio to receive either one of the standard-of-care physicians choice of PVd-Pomalidomide, Bortezomib, and Dexamethasone, DPd-Daratumumab, Pomalidomide, and Dexamethasone (N=211) or a single infusion of Cilta-cel administered after the physician’s choice of bridging therapy with PVd or DPd (N=208). In the standard-of-care group, DPd was administered in 28-day cycles and PVd in 21-day cycles until disease progression. Patients in the Cilta-cel group underwent apheresis, followed by at least one bridging therapy cycle, with the number of cycles based on patient clinical status and Cilta-cel manufacturing time, and lymphodepletion with Cyclophosphamide 300 mg/m2 IV and Fludarabine 30 mg/m2 IV daily for 3 days. Patients then received a single Cilta-cel infusion at a target dose of 0.75X106 CAR-positive T cells/kg of body weight 5-7 days after the initiation of lymphodepletion. The median age was 61 yrs, median time from diagnosis was 3.2 years, about 60% of patients had high risk cytogenetic abnormalities and all patients had received 1-3 previous lines of treatment. In the Cilta-cel group, 14.4% had triple-class drug resistance and 24.0% had resistance to anti-CD38 antibody. The Primary outcome was Progression Free Survival and Secondary outcomes sequentially tested included Complete Response (CR) or better, Overall Response Rate (ORR), Minimal Residual Disease (MRD) negativity, and Overall Survival (OS).

In the first interim analysis, a single Cilta-cel infusion resulted in a lower risk of disease progression or death, as well as rapid and deep responses, compared to standard therapies in Lenalidomide-refractory patients with multiple myeloma who had received one to three previous therapies

The researchers in this publication reported a prespecified second interim analysis of OS and an updated analysis of PFS in the intention-to-treat population. New data from the CARTITUDE-4 study highlight the significant clinical benefits of Cilta-cel in patients with Lenalidomide-refractory multiple myeloma who have received one to three prior lines of therapy.

Key Efficacy Findings

With a median follow-up of nearly 34 months patients receiving Cilta-cel experienced substantially longer disease control. Median PFS was not reached, compared with 11.8 months for those on standard therapy, representing a 71% reduction in the risk of progression or death.

Overall Survival outcomes also favored Cilta-cel. While median OS was not reached in either group, treatment with Cilta-cel led to a 45% reduction in the risk of death, a statistically significant improvement.

At 30 months, approximately 59% of Cilta-cel patients were alive and progression-free vs 26% with standard care. Around 66% remained treatment-free after a single infusion.

Cilta-cel achieved higher rates of sustained MRD negativity, indicating deeper and more durable responses.

Safety Overview

Safety outcomes were evaluated in 208 patients per group. Grade 3 Adverse Events (AEs) were 14% with Cilta-cel versus 37% with standard of care and Grade 4 AEs were 75% with Cilta-cel versus 56% with standard of care and was most commonly neutropenia in both groups. Treatment-Related Deaths was 3% with Cilta-cel and 2% with standard therapy. Most were linked to infections.

Why This Matters

CARTITUDE-4 is the first Phase 3 trial to demonstrate a significant Overall Survival benefit with CAR T-cell therapy in multiple myeloma. These findings reinforce the potential of Cilta-cel as an earlier-line treatment option. Even as newer therapies continue to emerge, Cilta-cel shows competitive, and in many cases superior outcomes, including notably higher MRD-negative response rates compared with other modern regimens.

Cilta-cel in lenalidomide-refractory multiple myeloma (CARTITUDE-4): an updated analysis including overall survival from an open-label, multicentre, randomised, phase 3 trial. Einsele H, San-Miguel J, Dhakal B et al. The Lancet Oncology, 2026;27:254-268

Reconsidering Menopausal Hormone Therapy in BRCA1/2 Carriers: Emerging Evidence Challenges Longstanding Concerns

RR

SUMMARY: Breast cancer is the most common cancer among women in the US and about 1 in 8 women (12%) will develop invasive breast cancer during their lifetime. It is estimated that in the US, approximately 321,910 new cases of female breast cancer will be diagnosed in 2026, and about 42,140 women will die of the disease, largely due to metastatic recurrence.

The tumor suppressor genes such as BRCA1 and BRCA2 help repair damaged DNA and thus play an important role in maintaining cellular genetic integrity, failing which these genetic aberrations can result in malignancies. Mutations in BRCA1 and BRCA2 account for about 20 to 25 percent of hereditary breast cancers and about 5 to 10 percent of all breast cancers. These mutations can be inherited from either of the parents and a child has a 50 percent chance of inheriting this mutation, and the deleterious effects of the mutations are seen even when a second copy of the gene in an individual is normal. Women with germline BRCA1 or BRCA2 mutations face markedly elevated lifetime risks of breast cancer, estimated at up to 70%. More than half of these cancers occur before the age of 50, underscoring the importance of informed counseling regarding risk-modifying exposures. 

For much of the latter half of the 20th century, Hormone Replacement Therapy (HRT) was widely prescribed to alleviate menopausal symptoms and protect against long-term complications such as osteoporosis. This practice shifted dramatically in 2002, when the Women’s Health Initiative reported increased risks of cardiovascular events and breast cancer associated with hormone therapy in older, postmenopausal women. In the aftermath, both patients and clinicians largely retreated from Menopausal Hormone Therapy (MHT), and its use declined sharply.

While those findings reshaped care in the general population, their applicability to women with hereditary cancer predisposition, particularly carriers of pathogenic BRCA1 or BRCA2 variants, has remained uncertain. These women face markedly elevated risks of ovarian and fallopian tube cancers and are therefore advised to undergo risk-reducing bilateral salpingo-oophorectomy at relatively young ages. The procedure is effective for cancer prevention but induces abrupt surgical menopause, often decades earlier than natural menopause, with well-documented short- and long-term consequences including vasomotor symptoms, sexual dysfunction, bone loss, and adverse cardiovascular and cognitive effects.

Menopausal Hormone Therapy (MHT) is the most effective intervention for mitigating these outcomes of early menopause. However, concerns that hormone exposure could further increase breast cancer risk in BRCA carriers have led to substantial hesitation, misinformation, and, in many cases, prolonged untreated symptoms. Researchers have emphasized, recommending premenopausal oophorectomy without offering a safe strategy to manage its consequences creates an untenable clinical dilemma.

Study Design: Emulating a Trial in a High-Risk Population

To address this evidence gap, investigators conducted the largest prospective matched analysis to date examining MHT use and breast cancer risk in BRCA1 and BRCA2 carriers. Using data from a longitudinal cohort, the study sought to emulate a randomized clinical trial by carefully matching women who initiated MHT after menopause, predominantly surgical menopause, to those who did not.

Eligible participants had no prior cancer history, no bilateral mastectomy, and had entered menopause. A total of 676 matched pairs were created, matched one-to-one by gene mutation (BRCA1 or BRCA2), year of birth, and age at menopause. Participants ranged in age from 22 to 76 years, with a mean age of 43.8 years. MHT formulations initiated after menopause included estrogen-only therapy, combined estrogen–progestogen therapy, progestogen alone, tibolone, and conjugated equine estrogen plus bazedoxifene. Cox proportional hazards models were used to estimate breast cancer risk.

Results: No Signal of Increased Breast Cancer Risk

After a mean follow-up of 5.6 years from the date of first MHT use, breast cancer incidence was significantly lower among women who used MHT compared with their matched, unexposed counterparts. Incident breast cancer occurred in 12.9% of MHT users versus 18.9% of non-users (P = 0.002).

Notably, estrogen-only therapy was associated with a substantial reduction in breast cancer risk, corresponding to a 63% relative decrease compared with non-users (HR=0·37; 95%: CI 0·24-0·57). In contrast, no increased or decreased risk was observed with combined estrogen–progestogen therapy, progestogen monotherapy, or tibolone. Among the 43 women who received conjugated equine estrogen plus bazedoxifene, no breast cancer diagnoses were reported during follow-up, an exploratory finding that warrants further investigation. Importantly, risk estimates were consistent across BRCA1 and BRCA2 carriers, underscoring the relevance of these findings across mutation subtypes.

Clinical Implications

These data provide critical reassurance for clinicians managing young women with hereditary breast and ovarian cancer syndromes. In contrast to earlier studies conducted in the general population, MHT use in BRCA1/2 carriers was not associated with an increased risk of breast cancer, regardless of formulation. Estrogen-only regimens, in particular, appeared protective, although causality cannot be inferred.

While limitations include a relatively modest follow-up duration and small numbers in certain subgroups, this prospective analysis offers the strongest evidence to date supporting the safety of MHT in this high-risk population. The findings reinforce the need for individualized, evidence-based counseling that balances cancer risk reduction with quality-of-life preservation.

Moving Forward

As MHT formulations continue to evolve, ongoing research will be essential to refine risk stratification and optimize menopause management strategies in BRCA mutation carriers. For now, these results support a personalized approach to MHT use in women experiencing surgical or natural menopause after risk-reducing oophorectomy, provided there are no contraindications. For many patients, informed use of MHT may offer not only symptom relief, but also a path toward improved long-term health and wellbeing without compromising breast cancer risk.

Menopausal Hormone Therapy and the Risk of Breast Cancer in Women with a Pathogenic Variant in BRCA1 or BRCA2. Kotsopoulos J, Seca M, Gronwald J, et al. J Natl Cancer Inst. 2025 Dec 17:djaf363. doi: 10.1093/jnci/djaf363. Epub ahead of print. PMID: 41403285.

Final Overall Survival Results from the EMBARK trial: Practice-Changing Evidence in High-Risk Biochemical Recurrence

RR

SUMMARY: Prostate cancer is the most common cancer in American men with the exclusion of skin cancer, and 1 in 9 men will be diagnosed with Prostate cancer during their lifetime. It is estimated that in the United States, about 333,830 new cases of Prostate cancer will be diagnosed in 2026 and 36,320 men will die of the disease. Androgen Deprivation Therapy (ADT) or testosterone suppression has been the cornerstone of treatment of advanced Prostate cancer, and is the first treatment intervention.

The major source of PSA (Prostate Specific Antigen) is the prostate gland, and the PSA levels are therefore undetectable within 6 weeks after Radical Prostatectomy. Similarly, following radiation therapy there is a gradual decline in PSA, before reaching a post treatment nadir. A detectable PSA level after Radical Prostatectomy, or a rising PSA level following radiation therapy, is considered PSA failure or biochemical recurrence. Approximately 35% of the patients with prostate cancer will experience PSA only relapse within 10 years of their primary treatment, and a third of these patients will develop documented metastatic disease within 8 years following PSA only relapse. Rising PSA is therefore a sign of recurrent disease. Patients with biochemically relapsed prostate cancer following local therapy, and a short PSA doubling time, are at risk for distant metastases.

Enzalutamide (XTANDI®) is a potent oral Androgen Receptor Pathway Inhibitor with demonstrated efficacy in patients with both localized and advanced prostate cancer.

EMBARK is a randomized, double-blind, placebo-controlled, multi-national, Phase III trial, conducted to evaluate the efficacy and safety of Enzalutamide plus Leuprolide and Enzalutamide monotherapy, as compared with Leuprolide alone, in patients with non-metastatic Hormone/Castration-Sensitive Prostate Cancer (nmHSPC or nmCSPC) prostate cancer, who have had high-risk biochemical recurrence. In this study, a total of 1068 eligible patients were randomly assigned 1:1:1 to receive Enzalutamide at 160 mg orally once daily plus Leuprolide IM every 12 weeks (N=355), single agent Enzalutamide at 160 mg orally once daily (N=355) or Leuprolide alone (N=358). All patients had received prior definitive therapy with radical prostatectomy and/or radiotherapy with curative intent. High risk disease was defined as a PSA doubling time of 9 months or less and a PSA level of 2 ng/ml above nadir after radiation therapy, or 1 ng/ml or more after radical prostatectomy with or without postoperative radiation therapy. The baseline characteristics were well balanced among the treatment groups. The median age was 69 years, the median PSA doubling time was 4.9 months and the median PSA level was 5.2 ng/ml. The Primary end point was Metastasis-Free Survival (MFS), as assessed by Blinded Independent Central Review (BICR) in the combination group, as compared with the Leuprolide-alone group. MFS is defined as the duration of time in months between randomization and the earliest objective evidence of radiographic progression by central imaging or death due to any cause, whichever occurred first. Secondary end points included MFS in the Enzalutamide monotherapy group, as compared with the Leuprolide-alone group, Overall Survival (OS), Patient-Reported Outcomes and Safety.

At a median follow up 60.7 months, the 5 year MFS was 87.3% in the Enzalutamide combination group and 71.4% with Leuprolide alone (HR for metastasis or death 0.42; P<0.001). This represented a 58% lower risk of metastasis or death in the combination group than Leuprolide alone among patients with biochemically recurrent prostate cancer. At the time of this analysis, Overall Survival data were immature.

In this publication, the final Overall Survival (OS) analysis of the Phase 3 EMBARK trial provided compelling long-term evidence supporting intensified Androgen-Receptor Pathway Inhibition in patients with high-risk biochemical recurrence of prostate cancer and no evidence of metastasis on conventional imaging. At the time of this final analysis, 277 deaths had occurred: 73 in the combination arm, 111 in the Leuprolide-alone arm, and 93 in the Enzalutamide monotherapy arm. Median follow-up exceeded 93 months across all treatment groups, offering a robust long-term perspective on survival outcomes.

Overall Survival: Durable and Clinically Meaningful Benefit

The combination of Enzalutamide plus Leuprolide demonstrated a statistically and clinically significant improvement in OS compared with Leuprolide alone:

  • 8-year OS:
    • 78.9% (95% CI, 73.9–83.1) with combination therapy
    • 69.5% (95% CI, 64.0–74.3) with Leuprolide alone
  • Hazard ratio for death: 0.60 (95% CI, 0.44–0.80; P<0.001)

This 40% relative reduction in mortality risk translates into an absolute improvement of nearly 10% at 8 years, a notable achievement in a population historically managed with Androgen Deprivation Therapy (ADT) alone.

By contrast, Enzalutamide monotherapy did not significantly improve OS relative to Leuprolide alone:

  • 8-year OS: 73.1% (95% CI, 67.6–77.9)
  • Hazard ratio: 0.83 (95% CI, 0.63–1.10; P=0.19)

While monotherapy previously demonstrated improvements in key Secondary endpoints, including Metastasis-Free Survival, it did not confer a statistically significant survival advantage in this final OS analysis.

Descriptive updates of Secondary endpoints were consistent with earlier reports. Time to first use of new antineoplastic therapy and time to first symptomatic skeletal event continued to favor combination therapy.

Although fractures were numerically more frequent in the combination arm, this reflected a broader category of bone and joint injuries. Importantly, the time to first symptomatic skeletal event was prolonged with Enzalutamide plus Leuprolide compared with Leuprolide alone, suggesting lower clinically meaningful skeletal morbidity despite the higher overall reporting of fractures.

Safety Profile: No New Signals

The long-term safety data remained consistent with earlier analyses. No new safety signals emerged, and the adverse-event profile of Enzalutamide, whether used in combination or as monotherapy, aligned with prior experience in metastatic castration-resistant and metastatic castration-sensitive prostate cancer settings.

Clinical Context: Imaging Evolution and Treatment Implications

Interpretation of these results must consider the evolving imaging landscape. At the time of trial enrollment, staging relied on CT or MRI for soft-tissue assessment and radionuclide bone scans for osseous disease. With the increasing use of PSMA PET imaging, it is likely that a proportion of patients categorized as nonmetastatic in the trial may have harbored occult locoregional or oligometastatic disease detectable by more sensitive modalities. Nevertheless, the study reflects real-world practice standards at the time and provides a pragmatic framework for treatment decision-making in high-risk biochemical recurrence.

Treatment Suspension Strategy: A Unique Feature

An important protocol component was treatment suspension at week 37 for patients achieving undetectable PSA (<0.2 ng/mL), with reinitiation upon PSA rise to predefined thresholds. This strategy aimed to mitigate toxicity and preserve quality of life. Notably, the OS benefit of combination therapy was achieved despite these mandated treatment interruptions.

Future research should clarify:

  • Which patients may safely undergo treatment suspension,
  • Whether continuous therapy could further optimize outcomes in select populations,
  • And how molecular imaging findings should inform early intensification strategies.

Positioning in the Treatment Paradigm

The final OS data reinforce earlier MFS findings and establish Enzalutamide plus ADT as a preferred standard of care for patients with Castration-Sensitive Prostate Cancer and high-risk biochemical recurrence without conventional radiographic metastases.

Although Enzalutamide monotherapy remains a reasonable option, particularly for patients prioritizing preservation of sexual function based on patient-reported outcomes, shared decision-making remains essential, balancing efficacy, toxicity, and quality-of-life considerations.

Conclusion

With nearly eight years of follow-up, the EMBARK trial confirms that intensification of Androgen-Receptor Pathway Inhibition with Enzalutamide plus Leuprolide delivers a durable Overall Survival advantage in high-risk biochemical recurrence. These findings extend the survival benefits observed with Enzalutamide across earlier disease states and further reshape management strategies in this evolving therapeutic space.

Improved Survival with Enzalutamide in Biochemically Recurrent Prostate Cancer. Shore ND, Luz MA, Giorgi UD, et al. N Engl J Med 2026;394:563-575.

Reassessing the Role of Radiotherapy in Locally Advanced Rectal Cancer: Insights from the CONVERT Trial

RR

SUMMARY: Colorectal cancer (CRC) is the third most common cancer diagnosed in both men and women in the United States. The American Cancer Society estimates that approximately 49,990 new cases of rectal cancer CRC will be diagnosed in the United States in 2026.

The management of Locally Advanced Rectal Cancer (LARC) has historically relied on a multimodality approach centered on neoadjuvant chemoradiotherapy (nCRT), followed by total mesorectal excision and adjuvant chemotherapy. While this paradigm has improved local control, it comes at the cost of treatment-related morbidity, particularly long-term bowel, urinary, and sexual dysfunction. As systemic therapies and surgical techniques have advanced, the necessity of routine radiotherapy, especially in biologically lower-risk disease, has come under increasing scrutiny.

In this context, neoadjuvant chemotherapy (nCT) has emerged as a potential strategy to reduce treatment burden without compromising oncologic outcomes. Total Neoadjuvant Therapy (TNT) has gained traction, supported by trials such as RAPIDO and PRODIGE 23, particularly for patients with high-risk features. However, as outcomes improve and local recurrence rates decline, the routine use of pelvic radiotherapy in all patients is increasingly being questioned, especially in those with more favorable disease biology.

CONVERT is a randomized, open-label, multicenter, Phase III study, designed to address this clinical gap by focusing specifically on patients with LARC and uninvolved mesorectal fascia (MRF), a subgroup with a more favorable risk profile for local recurrence. This study enrolled 663 patients, of whom 589 received protocol-directed therapy. Enrolled patients had LARC within 12 cm from the anal verge.  Patients were assigned to receive either Neoadjuvant chemotherapy (nCT) with 4 cycles of CAPOX chemotherapy alone (N=300), or nCRT which was standard CRT with Capecitabine concurrently (N=289). The Primary end point was 3-year LocoRegional Recurrence-Free Survival (LRRFS). Secondary end points included 3-year Disease-Free survival (DFS), 3-year Overall Survival (OS), and Safety.

At a median follow-up of 48 months, both treatment strategies achieved excellent local control.

  • 3-year LRRFS: 96.3% (nCT) vs 97.4% (nCRT)
  • 3-year DFS: 89.2% vs 87.9%
  • 3-year OS: 95.0% vs 94.1%

Although the study did not formally meet its predefined noninferiority margin, this was largely driven by unexpectedly low recurrence rates in both arms, reflecting advances in surgical technique and perioperative care.

Toxicity and Quality of Life: A Key Differentiator

nCT was associated with a significantly lower incidence of long-term grade 2–4 adverse events (16.0% vs 26.3%) and reduced rates of proctitis.

These findings highlight a critical trade-off: while oncologic outcomes appear comparable in selected patients, radiotherapy contributes substantially to long-term morbidity, further supporting a treatment de-escalation strategy in appropriately selected patients.

From a survivorship perspective, avoiding radiation may:

  • Reduce chronic bowel dysfunction and low anterior resection syndrome–like symptoms
  • Lower the risk of radiation dermatitis and pelvic fibrosis
  • Potentially decrease the risk of secondary malignancies
  • Preserve fertility and ovarian function in younger patients

Potential candidates for nCT alone:

  • MRF-negative tumors
  • cT2–T3 disease without extensive nodal burden
  • Patients prioritizing quality of life and toxicity reduction

Patients who likely still require radiotherapy:

  • MRF-involved disease
  • T4b tumors
  • High-risk nodal disease

Exploratory findings also suggest caution in:

  • Tumors located <5 cm from the anal verge, where local control may be more challenging

Taking a risk-adapted Approach:

  • High-risk disease → TNT including radiotherapy
  • Intermediate-risk → selective radiotherapy strategies
  • Lower-risk (MRF-negative) → potential chemotherapy-alone approaches

Limitations and Future Directions

Several considerations remain:

  • Open-label design and modified intention-to-treat population
  • Lack of molecular stratification (e.g., mismatch repair status)
  • Rapidly evolving standards, including immunotherapy for dMMR disease

Future studies will need to integrate molecular profiling, imaging, and patient preferences to refine treatment selection further.

Clinical Takeaways

  • nCT with CAPOX achieved comparable DFS and OS to nCRT in MRF-negative LARC
  • Noninferiority was not formally met, but outcomes were influenced by very low recurrence rates
  • Significantly reduced long-term toxicity supports a de-escalation approach
  • Findings are consistent with NCCN and ASCO guidance supporting selective omission of radiotherapy in carefully chosen patients

Conclusion: Toward a More Individualized Treatment Paradigm

The CONVERT trial adds important prospective evidence supporting the selective omission of radiotherapy in LARC. While not practice-changing in isolation, it strengthens a growing movement toward precision-based, risk-adapted care, balancing oncologic efficacy with long-term quality of life. As guidelines continue to evolve, the challenge will be to identify the right patient for the right treatment intensity, ensuring optimal outcomes without unnecessary toxicity.

Neoadjuvant Chemotherapy With CAPOX Versus Chemoradiation for Locally Advanced Rectal Cancer With Uninvolved Mesorectal Fascia (CONVERT): Final Results of a Phase III Trial. Mei W-J, Wang X-Z, Zhang X, et al. J Clin Oncol. 2026;44: 970-980.

New Treatment Guidelines for Multiple Myeloma

RR

SUMMARY: Multiple Myeloma (MM) is a clonal disorder of plasma cells in the bone marrow and the American Cancer Society estimates that in the United States, 36,000 new cases will be diagnosed in 2026, and 10,850 patients are expected to die of the disease.

Recommendations on the treatment of multiple myeloma, was first published jointly by ASCO and Cancer Care Ontario in 2019. These two organizations jointly updated these recommendations to provide guidance, following the introduction of new therapies and review of 161 relevant randomized trials.

This clinical practice guideline update focused on four topics.

Smoldering Multiple Myeloma:
1.1. Patients with high-risk smoldering multiple myeloma may be offered active monitoring or Daratumumab (for up to 36 months). Lenalidomide is not routinely recommended.

Qualifying Statements for Recommendation 1.1:
In the AQUILA trial, high-risk smoldering multiple myeloma was defined as ≥10% clonal plasma cells in bone marrow and at least one of the following: (1) a serum M-protein level of at least 3 g/dl; (2) IgA smoldering multiple myeloma; (3) immunoparesis with reduced levels of two uninvolved immunoglobulin isotypes; (4) a ratio of involved FLCs to uninvolved FLCs (FLC ratio) in serum of 8 to <100; (5) a percentage of clonal plasma cells in bone marrow of more than 50% to <60%.
It should be noted that this definition differs from other contemporary criteria for high-risk smoldering multiple myeloma and that using the AQUILA definition of high-risk may classify some patients as high-risk who would not meet high-risk criteria in other classification systems. Therefore, careful discussion and consideration of individual patient factors is essential when evaluating management options.

1.2. Therapy is not recommended for patients with smoldering multiple myeloma who are not at high risk

1.3. Active multiple myeloma should be excluded using current diagnostic algorithms and procedures for smoldering multiple myeloma.


Transplant-Eligible MM: Evaluation of Eligibilty
2.1.1. Unless clearly ineligible, patients should be referred to a transplant center at time of diagnosis to determine transplant eligibility.

2.1.2. Eligibility for Autologous Stem Cell Transplantation (ASCT) should not be based solely on a patient’s chronological age or renal function. Instead, a comprehensive assessment of overall health, performance status, frailty, and comorbidities should guide the decision.

Transplant-Eligible MM: Initial Therapy
2.2.1. Transplant-eligible patients should be offered 4 months of induction therapy with either Daratumumab or Isatuximab, each in combination with Bortezomib, Lenalidomide, and Dexamethasone.

Qualifying Statement for Recommendation 2.2.1: In areas where Lenalidomide may be difficult to obtain, Thalidomide is a reasonable substitute in Daratumumab-containing regimens. At least four cycles of therapy should be considered the baseline, but patients can receive more cycles if they must wait for transplant.

2.2.2. For patients who received Daratumumab, Bortezomib, Lenalidomide, and Dexamethasone and planned to receive post-transplant consolidation, two cycles of Daratumumab, Bortezomib, Lenalidomide, and Dexamethasone can be offered following induction therapy and stem cell transplantation.

2.2.3. Carfilzomib can be used as a substitute for Bortezomib in the recommended induction and consolidation regimens, if toxicity is a concern.

Transplant-Eligible MM: Conditioning and Transplant
2.3.1. Up-front transplantation should be offered to all transplant-eligible patients.

2.3.2. Agents associated with stem-cell toxicity such as Melphalan should be avoided in patients who are potential candidates for ASCT.

2.3.3. Regardless of transplant intent, ample stem cells (sufficient for at least two ASCT) should be collected following 4-6 months of induction therapy to allow for potential stem cell transplants later.

2.3.4. High-dose Melphalan is the recommended conditioning regimen for ASCT.

Transplant-Eligible MM: Maintenance
2.4.1. Lenalidomide should be offered as maintenance therapy.

2.4.2. Carfilzomib or Daratumumab may be added to Lenalidomide with or without Dexamethasone.

Transplant-Eligible MM: Measurement of Response
2.5.1. Depth of response should be assessed with each cycle using IMWG criteria as a guideline. Frequency of assessment may be less frequent but at minimum every 3 months, once best response is attained or while receiving maintenance therapy.
MRD status may be valuable in assessing depth of response but should not be relied on as the sole measure.
Whole-body low-dose CT scan, FDG PET/CT and/or diffusion-weighted MRI are the recommended methods for assessing bone lesions at baseline and during surveillance.


Transplant-Ineligible MM: Therapy
3.1.1. A CD38-targeted monoclonal antibody (Daratumumab OR Isatuximab) in combination with Bortezomib, Lenalidomide, and Dexamethasone should be offered to transplant-ineligible patients who are not frail and can tolerate therapy.

3.1.2. Daratumumab, Lenalidomide, and Dexamethasone OR Bortezomib, Lenalidomide, and Dexamethasone are reasonable alternatives in transplant-ineligible patients who are not suitable candidates for quadruplet therapy

Transplant-Ineligible MM: Goals of Therapy and Measurement of Response
3.2.1. The goal of initial therapy for transplant-ineligible patients should be achievement of the best quality and depth of response. Depth of response for all patients should be assessed per Recommendation 2.5.1 regardless of transplant eligibility.

3.2.2. Upon initiation of therapy, one should define patient-specific goals of therapy. Quality of life (including symptom management and tolerability of treatment) should be assessed at each visit to determine if the goals of therapy are being maintained/met, and this should influence the intensity and duration of treatment. The goals should be redefined periodically, based on response, symptoms, and quality of life.

3.2.3. Patients should be monitored closely with consideration of dose modifications based on levels of toxicity, neutropenia, fever/infection, tolerability of adverse effects, performance status, liver and kidney function, and in keeping with the goals of treatment.

 

Relapsed/Refractory MM: Therapy
4.1. Treatment of biochemically relapsed myeloma should be individualized. Factors to consider include patient’s tolerance of prior treatment, rate of rise of myeloma markers, cytogenetic risk, presence of comorbid conditions (ie, renal insufficiency), frailty, and patient preference.

4.2. All relapsed patients with disease-related symptoms due to myeloma should be treated immediately.

4.3. Triplet therapy or T-cell redirecting therapies should be offered to eligible patients with relapsed/refractory multiple myeloma based on the following principles:
a) Whenever possible, patients should be offered treatment regimens that include agents that are different than those in their prior therapies.
b) Triplets should be offered to eligible patients.
c) CAR T-cell therapy should be offered to eligible patients. A thorough patient-centered discussion regarding the risks, benefits, and timing of CAR T-cell therapy is advised.
d) Patient preferences with respect to toxicity tolerance, dose and schedule convenience, and means of administration should be factored in with shared decision making when deciding between triplet or CAR T-cell therapy.
e) CAR T-cell therapy may not be appropriate for patients with rapidly progressive relapsed myeloma given the time required for CAR T-cell manufacturing. In this setting, an agent that is immediately available may be favored over CAR T-cell therapy.
f) If the patient is unable to receive triplet or CAR T-cell therapy (based on tolerability, frailty, access, etc), doublet therapy is reasonable.
g) Bispecific antibodies should be offered to eligible patients (including older and frail patients).
h) The optimal sequencing of therapy is an evolving consideration. In the context of a limited evidence base, sequencing decisions should be made based on patient factors, disease characteristics, mechanism of action, and prior treatment responses.
i) Patients for whom existing options have been exhausted or for whom the risks are likely to outweigh the benefits should be offered best supportive care and hospice referral.

4.4.1. ASCT, if not previously received, may be offered to transplant-eligible patients with relapsed multiple myeloma.

4.4.2. Repeat ASCT should not be offered in relapsed multiple myeloma unless the patient experienced a long remission (typically considered >4-5 years) from first transplant.

Treatment of Multiple Myeloma: ASCO–Ontario Health (Cancer Care Ontario) Living Guideline. Hicks LK,  Messersmith HJ, Hadidi SA, et al. J Clin Oncol. 2026;44:914-941.

 

FDA Approves OPDIVO® with Chemotherapy for Previously Untreated Hodgkin Lymphoma

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SUMMARY: The FDA on March 20, 2026, approved Nivolumab (OPDIVO®) with Doxorubicin, Vinblastine, and Dacarbazine (AVD) for adult and pediatric patients 12 years and older with previously untreated, Stage III or IV classical Hodgkin lymphoma (cHL).

The American Cancer Society estimates that in the United States for 2026, about 8920 new cases of Hodgkin Lymphoma will be diagnosed, and about 1100 patients will die of the disease. Hodgkin Lymphoma is classified into two main groups – Classical Hodgkin Lymphomas and Nodular Lymphocyte Predominant type, by the World Health Organization. The Classical Hodgkin Lymphomas include Nodular sclerosing, Mixed cellularity, Lymphocyte rich, Lymphocyte depleted, subtypes and accounts for approximately 10% of all malignant lymphomas. Nodular sclerosis Hodgkin lymphoma histology, accounts for approximately 80% of Hodgkin Lymphoma cases in older children and adolescents in the United States. Classical Hodgkin Lymphoma is a malignancy of primarily B lymphocytes and is characterized by the presence of large mononucleated Hodgkin and giant multinucleated Reed-Sternberg (RS) cells collectively known as Hodgkin and Reed-Sternberg cells (HRS).

For patients with Hodgkin Lymphoma, the goal of first-line chemotherapy is cure. Advanced stage (Stage III-IV) Classical Hodgkin lymphoma has a cure rate of approximately 70-80% when treated in the first-line setting with a combination of Doxorubicin, Bleomycin, Vinblastine, and Dacarbazine (ABVD). This regimen which was developed more than 40 years ago is less expensive, easy to administer, is generally well tolerated and is often used in first line setting. Nonetheless, this regimen which contains Bleomycin can cause pulmonary toxicity, the incidence of which is higher in older patients and in those who receive consolidation radiotherapy to the thorax.

Brentuximab Vedotin (ADCETRIS®) is an Antibody-Drug Conjugate (ADC) that targets CD30, which is a surface antigen, expressed on Reed-Sternberg cells, in patients with Classical Hodgkin lymphoma. This ADC consists of an anti-CD30 monoclonal antibody linked to MonoMethyl Auristatin E (MMAE), an antimicrotubule agent. Upon binding to the CD30 molecule on the cancer cells, MMAE is released into the cancer cell, resulting in cell death. In the ECHELON-1 study, frontline treatment with Brentuximab Vedotin (BV) in combination with Doxorubicin, Vinblastine and Dacarbazine (AVD) resulted in a significant improvement both in Progression Free Survival as well as Overall Survival, after a median follow up of 6 years. However, frontline BV adds toxicity, and 7-20% of patients still develop Relapsed/Refractory Hodgkin Lymphoma.

The most common genetic abnormality in Nodular sclerosis subtype of Hodgkin lymphoma is the selective amplification of genes on the short arm of chromosome 9 (9p24.1) which includes JAK-2, with resulting increased expression of PD-1 ligands such as PDL1 and PDL2 on HRS cells, as well as increased JAK-STAT activity, essential for the proliferation and survival of Hodgkin Reed-Sternberg (HRS) cells.

Nivolumab (OPDIVO®) is a fully human, immunoglobulin G4 monoclonal antibody that binds to the PD-1 receptor and blocks its interaction with PD-L1 and PD-L2, thereby undoing PD-1 pathway-mediated inhibition of the immune response and unleashing the T cells.

SWOG S1826 was an open-label, randomized Phase III trial conducted to compare the combination of Nivolumab plus AVD, to Brentuximab Vedotin plus AVD, in adolescent and adult patients with previously untreated advanced-stage classical Hodgkin Lymphoma (cHL). In this study, 976 newly diagnosed Stage III or IV cHL patients (N=976) were randomly assigned 1:1 to receive either 6 cycles of Nivolumab at 240 mg IV on days 1 and 15 (N=489) or Brentuximab Vedotin 1.2 mg/kg IV on days 1 and 15 (N=487). Both treatment groups also received AVD (Doxorubicin, Vinblastine, Dacarbazine ) IV on days 1 and 15, and treatment was repeated every 28 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Granulocyte-Colony Stimulating Factor (G-CSF) Pegfilgrastim SC on days 2 and 16, or Filgrastim SC on days 6-10 and 21-25 was optional in the Nivolumab group (N-AVD) but was required in the Brentuximab Vedotin group (BV-AVD). Approximately 54% in the N-AVD group received G-CSF compared to 95% in the BV-AVD group. After completion of cycle 6, patients could receive radiation therapy at the discretion of the treating physician, to metabolically active residual lesions noted on the end of treatment PET. Less than 1% of patients across both treatment groups had received radiotherapy. Patients were stratified by age, International Prognostic Score (IPS) and intent to use radiation therapy. The median age was 27 years, 24% of patients were less than 18 yrs, 76% were Caucasian, 55% were men, 64% had Stage IV disease and 32% had IPS of 4-7. The Primary endpoint was Progression Free Survival (PFS). Secondary endpoints included Overall Survival (OS), Event-Free Survival (EFS), Patient-Reported Outcomes (PROs), and Safety.

Sustained Progression-Free Survival Benefit at 3 Years

With a median follow-up of 3.1 years, updated data continue to reinforce the clinical advantage of N-AVD over BV-AVD in patients with advanced-stage classical Hodgkin lymphoma (cHL). The 3-year PFS rate reached 91% with N-AVD, compared with 82% with BV-AVD, translating to a 52% reduction in the risk of progression or death (HR 0.48; P< 0.0001).

Consistent Benefit Across Key Patient Subgroups

The PFS advantage with N-AVD was maintained irrespective of age, disease stage, or baseline risk, as defined by the International Prognostic Score (IPS):

  • Adolescents (12–17 years): 93% vs 82%
  • Adults (18–60 years): 91% vs 85%
  • Older patients (>60 years): 82% vs 58%
  • Stage III disease: 93% vs 86%
  • Stage IV disease: 89% vs 80%
  • IPS 0–3: 92% vs 84%
  • IPS 4–7: 87% vs 77%

Notably, outcomes in Stage IV disease with N-AVD approached those seen in Stage III, highlighting the regimen’s efficacy even in higher disease burden settings. These findings further support current guideline positioning of N-AVD as a preferred frontline treatment approach in advanced-stage disease.

Event-Free and Overall Survival Trends

Beyond PFS, N-AVD also demonstrated a statistically significant improvement in EFS (HR 0.56; P =0.0004). While OS data remain immature, an encouraging trend favoring N-AVD has emerged:

  • 3-year OS: 98% (N-AVD) vs 97% (BV-AVD)
  • Deaths observed: 8 vs 15, respectively

Longer follow-up will be essential to determine whether this early signal translates into a definitive survival advantage.

Safety Profile: Favorable and Manageable

No new safety signals were identified with extended follow-up, reinforcing the tolerability of the N-AVD regimen. Key safety observations include Lower incidence of second malignancies with N-AVD (1.2% vs 2.3%) with BV-AVD. Immune-related adverse events were generally infrequent and peripheral neuropathy was less frequent with N-AVD (7% vs 14%), reflecting reduced neurotoxicity compared with BV-containing therapy. Higher rates of grade ≥3 events occurred with N-AVD (48.4% vs 30.5%), but was not associated with increased infectious complications. G-CSF use was mandatory with BV-AVD but optional with N-AVD, influencing observed rates.

Unique Trial Design: Inclusion of Adolescent Patients

This study represents a landmark effort in Hodgkin lymphoma research, as it is the first large-scale trial to enroll both adolescents and adults in the frontline setting, and adolescents in this trial constituted the largest cohort in which a checkpoint inhibitor has been evaluated as part of initial therapy, providing important insights into younger patient populations.

Clinical Implications and Future Directions

These long-term results confirm that the integration of immune checkpoint blockade into frontline therapy yields durable disease control with a manageable safety profile.

Nivolumab plus AVD:

  • Provides sustained remission benefits
  • Demonstrates consistent efficacy across risk groups
  • Reduces certain long-term toxicities, including neuropathy and second cancers

Collectively, the data support N-AVD as a new standard of care for patients with advanced-stage cHL. Ongoing follow-up will further clarify Long-term overall survival outcomes, Late toxicities and Patient-reported outcomes

Key Takeaways

  • N-AVD significantly improves 3-year PFS vs BV-AVD (91% vs 82%)
  • Benefit is consistent across age, stage, and risk categories
  • EFS is significantly improved; OS data are trending positive
  • Safety profile is favorable, with reduced neuropathy and fewer second malignancies
  • Findings reinforce N-AVD as a preferred frontline regimen in advanced-stage cHL

3-year follow-up of the S1826 study confirms improved progression-free survival with nivolumab-AVD compared to brentuximab vedotin-AVD in advanced stage classic Hodgkin lymphoma. Herrera A, Leblanc M, Castellino S, et al. Blood (2025) 146 (Supplement 1):151. doi: 10.1182/blood-2025-151.

FDA Approves LIFYORLI® with nab-Paclitaxel for Platinum-Resistant Ovarian Cancer

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SUMMARY: The FDA on March 25, 2026, approved Relacorilant (LIFYORLI®), a glucocorticoid receptor antagonist, in combination with nab-Paclitaxel for the treatment of adults with platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer who have received one to three prior systemic treatment regimens, at least one of which included Bevacizumab.

It is estimated that in the United States, approximately 21,010 women will be diagnosed with ovarian cancer in 2026 and 12,450 women will die of the disease. Ovarian cancer ranks fifth in cancer deaths among women. It accounts for more deaths than any other cancer of the female reproductive system. Approximately 75% of the ovarian cancer patients are diagnosed with advanced disease. Patients with newly diagnosed advanced ovarian cancer are often treated with platinum-based chemotherapy following primary surgical cytoreduction. Approximately 70% of these patients will relapse within the subsequent 3 years and are incurable, with a 5-year Overall Survival rate of about 20-30%.

Background: Persistent Unmet Need in PROC

Platinum-Resistant Ovarian Cancer (PROC) remains one of the most challenging clinical scenarios in gynecologic oncology, with historically poor outcomes and a median Overall Survival ranging from approximately 10 to 17 months in clinical trials. Therapeutic options have been limited and largely consist of single-agent chemotherapy, with or without Bevacizumab, as well as select biomarker-driven therapies such as Mirvetuximab soravtansine (ELAHERE®) for Folate Receptor α (FRα)-positive disease and Trastuzumab Deruxtecan ENHERTU&reg;) for HER2-positive tumors. However, these targeted approaches apply only to a subset of patients, underscoring the need for broadly applicable strategies.

A Novel Therapeutic Approach: Targeting the Glucocorticoid Receptor

Relacorilant introduces a first-in-class mechanism in ovarian cancer as a Selective Glucocorticoid Receptor Antagonist (SGRA). Cortisol signaling through the glucocorticoid receptor promotes tumor survival by upregulating anti-apoptotic pathways, thereby contributing to chemotherapy resistance. By selectively inhibiting this pathway, Relacorilant enhances tumor sensitivity to cytotoxic agents. Importantly, the glucocorticoid receptor is expressed in more than 95% of epithelial ovarian cancers, distinguishing this approach from biomarker-restricted therapies and enabling a potential “all-comers” strategy.

ROSELLA Trial Design

The Phase 3 ROSELLA trial was a global, randomized, open-label study evaluating Relacorilant in combination with nab-Paclitaxel versus nab-Paclitaxel alone in patients with Platinum-Resistant Ovarian Cancer (PROC).

  • Study Population: 381 patients with 1-3 prior lines of therapy; all previously treated with Bevacizumab
  • Intervention: Relacorilant 150 mg orally,  day before, day of, and day after nab-Paclitaxel plus nab-Paclitaxel 80 mg/m2 IV on days 1, 8, and 15 of each 28-day cycle (N=188)
  • Comparator: Nab-paclitaxel monotherapy 100 mg/m2 IV on the aforementioned schedule (N=193)
  • Primary Endpoints: Progression-free survival (PFS) by blinded independent central review and overall survival (OS)
  • Follow-up: Median of 24.8 months

Baseline characteristics were well balanced, with a heavily pretreated population, 61% had prior PARP inhibitor exposure and 44% had received three prior lines of therapy.

Efficacy: Dual Primary Endpoints Achieved

ROSELLA met both Primary endpoints, demonstrating clinically meaningful improvements in survival outcomes:

Overall Survival

  • Median OS: 16.0 vs 11.9 months
  • Hazard ratio (HR): 0.65 (35% reduction in risk of death)
  • 18-month OS: 46% vs 27%
  • Statistical significance: P=0.0004

Progression-Free Survival

  • Median PFS: 6.5 vs 5.5 months
  • HR: 0.70
  • Statistical significance: P≈0.008

The survival benefit was consistent across all prespecified subgroups, including patients with poor prognostic features. Notably, second PFS was also improved, suggesting that the benefit of Relacorilant extends beyond first progression.

Safety and Tolerability

The addition of Relacorilant did not introduce new safety signals and was generally well tolerated. The adverse event profile was consistent with known toxicities of nab-Paclitaxel. Common adverse events were neutropenia, anemia, fatigue, and nausea. Overall, the regimen demonstrated a favorable risk–benefit profile.

Clinical Context and Positioning

The results of ROSELLA are particularly notable in the context of prior studies in PROC. For example:

  • The addition of Bevacizumab in earlier trials improved PFS but not Overall Survival
  • Immune checkpoint inhibitors have shown limited benefit in unselected PROC populations, with modest gains in select biomarker-defined subsets
  • Biomarker-driven therapies such as FRα- and HER2-targeted agents remain restricted to smaller patient populations

In contrast, Relacorilant offers a biomarker-independent approach, with broad applicability and a demonstrated survival advantage. Furthermore, all patients in ROSELLA had prior Bevacizumab exposure, reflecting contemporary treatment patterns and enhancing the real-world relevance of the findings.

Mechanistic and Translational Insights

Exploratory analyses from earlier-phase studies suggest that the benefit of Relacorilant is independent of the level of glucocorticoid receptor expression, supporting its use without biomarker selection. Ongoing and future studies will further refine understanding of predictive biomarkers, including receptor expression, cortisol dynamics, and pathway activation signatures.

Limitations

Key limitations of the ROSELLA trial include:

  • Open-label design (mitigated by objective endpoints and blinded PFS assessment)
  • Limited data in patients with more than three prior lines of therapy
  • Underrepresentation of certain racial and ethnic groups
  • Limited conclusions for rare histologic subtypes

Despite these considerations, the robustness of the dataset, including mature OS data and balanced post-progression therapies, supports the validity of the findings.

Clinical Implications

ROSELLA represents a meaningful advance in the management of Platinum-Resistant Ovarian Cancer (PROC). The combination of Relacorilant and nab-Paclitaxel is the first regimen in this setting to demonstrate a significant improvement in both Progression-Free and Overall Survival compared with a weekly taxane backbone.

With a 35% reduction in mortality risk and a median Overall Survival gain exceeding 4 months, this regimen has the potential to redefine the treatment paradigm for PROC, particularly given its applicability without the need for biomarker testing.

Key Takeaways

  • Relacorilant introduces a novel mechanism targeting glucocorticoid receptor–mediated chemotherapy resistance
  • ROSELLA demonstrated significant improvements in both OS and PFS
  • Benefit was consistent across subgroups, including heavily pretreated patients
  • The regimen is well tolerated with no new safety concerns
  • Represents a potential new standard of care in Platinum-Resistant Ovarian Cancer without biomarker restriction

Overall survival with relacorilant and nab-paclitaxel in patients with platinum-resistant ovarian cancer (ROSELLA): a phase 3 randomised controlled trial. Lorusso D, Gladieff L, O’Malley D et al. The Lancet 2026; DOI: 10.1016/S0140-6736(26)00462-9

Teclistamab Plus Daratumumab Sets a New Standard of Care in Early Relapsed or Refractory Myeloma

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SUMMARY: Multiple Myeloma is a clonal disorder of plasma cells in the bone marrow and the American Cancer Society estimates that in the United States, 36,000 new cases will be diagnosed in 2026, and 10,850 patients are expected to die of the disease. Multiple Myeloma is a disease of the elderly, with a median age at diagnosis of 69 years and characterized by intrinsic clonal heterogeneity. Almost all patients eventually will relapse, and patients with a high-risk cytogenetic profile, extramedullary disease or refractory disease have the worst outcomes. The introduction of Proteasome Inhibitors, Immunomodulatory agents and CD38 targeted therapies has resulted in higher Response Rates, as well as longer Progression Free Survival (PFS) and Overall Survival (OS), with the median survival for patients with myeloma approaching 10 years or more. Nonetheless, multiple myeloma in 2025 remains an incurable disease.

Relapsed or Refractory Multiple Myeloma (RRMM) remains a complex clinical challenge, even as therapeutic options continue to expand. Progressive immune dysfunction, cumulative treatment toxicity, and repeated relapses often limit the durability of benefit with conventional salvage regimens. Moreover, the increasingly effective frontline landscape has raised the bar for second- and later-line therapy, leaving fewer highly active, well-tolerated options for patients early in relapse.

BCMA-directed therapies have transformed expectations in advanced disease, particularly with CAR-T cell approaches demonstrating deep responses and prolonged disease control. However, manufacturing timelines, resource intensity, and patient fitness requirements limit universal access. Consequently, there is a critical need for off-the-shelf, immunotherapy-based regimens that deliver CAR-T–like efficacy with broader applicability.

Teclistamab (TECVAYLI®), a bispecific T-cell engaging antibody targeting CD3 on T cells and BCMA on myeloma cells, has previously shown meaningful and durable responses in heavily pretreated RRMM. Daratumumab (DARZALEX®), an anti-CD38 monoclonal antibody, remains a foundational therapy across all disease stages, offering both direct antimyeloma activity and immune modulation. Preclinical and clinical observations suggest that Daratumumab-mediated depletion of immunosuppressive cellular subsets enhances T-cell fitness, providing a strong biological rationale for combination with BCMA-directed bispecific antibodies.

The MajesTEC-3 trial was designed to test whether combining Teclistamab with Daratumumab could improve outcomes compared with established Daratumumab-based regimens in patients with earlier-line RRMM.

Study Design and Patient Population

MajesTEC-3 (NCT05083169) is an ongoing, randomized, open-label, Phase 3 trial conducted across 150 centers in 20 countries. Eligible patients had relapsed or refractory multiple myeloma after one to three prior lines of therapy, including prior exposure to both an immunomodulatory agent and a proteasome inhibitor. Patients with prior BCMA-directed therapy or anti-CD38–refractory disease were excluded.

A total of 587 patients were randomized 1:1 to receive either:

  • Teclistamab plus subcutaneous Daratumumab, or
  • Investigator’s choice of standard Daratumumab-based therapy, consisting of Daratumumab and Dexamethasone combined with either Pomalidomide (DPd) or Bortezomib (DVd).

Randomization was stratified by choice of control regimen, International Staging System stage, prior exposure to anti-CD38 antibodies, and number of prior treatment lines. The median patient age was approximately 64–65 years, with a median of two prior lines of therapy. Importantly, more than one-third of enrolled patients had high-risk cytogenetic features, reflecting a clinically relevant population.

Treatment Administration: A Patient-Centered, Steroid-Sparing Approach

Patients in the investigational arm received subcutaneous Teclistamab using a step-up dosing strategy, followed by a progressively extended dosing interval, transitioning to monthly administration from cycle 7 onward. Daratumumab was administered subcutaneously according to its approved schedule.

Notably, the regimen became steroid-free after cycle 1, an important quality-of-life consideration for patients requiring long-term therapy. Infection prophylaxis, immunoglobulin supplementation, and monitoring of IgG levels were mandated, with protocol amendments reinforcing best practices for infection prevention during BCMA-directed therapy. The Primary end point was Progression-Free Survival (PFS), as assessed by an Independent Review Committee.

Primary Endpoint: Striking Improvement in Progression-Free Survival

At a median follow-up of 34.5 months, Teclistamab plus Daratumumab demonstrated a highly significant and clinically transformative improvement in PFS compared with DPd or DVd.

  • The estimated 36-month PFS rate was 83.4% with Teclistamab–Daratumumab versus 29.7% with standard Daratumumab-based therapy.
  • This translated into an 83% reduction in the risk of disease progression or death (HR 0.17; 95% CI, 0.12–0.23; P<0.001).
  • The prespecified boundary for superiority was crossed at the first interim analysis.

Importantly, the PFS advantage was consistent across all prespecified and clinically relevant subgroups, including patients with high-risk cytogenetics and those treated in earlier versus later relapse.

Depth and Durability of Response

Beyond delaying progression, Teclistamab–Daratumumab induced exceptionally deep and durable responses:

  • Complete Response or better was achieved in 81.8% of patients receiving the combination, compared with 32.1% in the control arm.
  • Overall Response Rates were also higher (89.0% vs. 75.3%).
  • Rates of Minimal Residual Disease negativity at a sensitivity of 10⁻⁵ were more than threefold higher with Teclistamab–Daratumumab (58.4% vs. 17.1%).

Responses occurred rapidly, with a median time to first response of just over one month, and deepened over time. At three years, nearly 90% of responders in the investigational arm remained in response, suggesting the emergence of a plateau in disease control.

Overall Survival and Symptom Outcomes

Although follow-up for overall survival continues, early analyses favored Teclistamab–Daratumumab, with a high proportion of patients remaining alive beyond two years. Improvements were also observed in time to worsening of myeloma-related symptoms, underscoring the regimen’s clinical and patient-reported benefit.

Safety and Tolerability: Manageable With Established Protocols

The safety profile of Teclistamab–Daratumumab was consistent with the known risks of BCMA-directed bispecific antibodies and Daratumumab. Serious adverse events occurred more frequently in the investigational arm, driven primarily by cytopenias and infections.

  • Cytokine Release Syndrome was common but predominantly low grade and largely confined to the step-up dosing period.
  • Importantly, the incidence of CRS was lower than that reported with Teclistamab monotherapy, supporting a favorable interaction between the two agents.
  • Fatal adverse events were infrequent and decreased following protocol-reinforced infection-prevention strategies.

The trial highlights the critical importance of early immunoglobulin replacement, antimicrobial prophylaxis, and vigilant monitoring, now well established in guidelines for patients receiving BCMA-targeted therapies.

Context Within the Evolving Treatment Landscape

The magnitude of benefit observed with Teclistamab–Daratumumab is particularly notable given the strong performance of the control arm, which exceeded historical expectations from prior DPd and DVd studies. Even in this context, the combination delivered superior depth, durability, and consistency of response. As CAR-T therapies move earlier in the disease course, off-the-shelf immunotherapies such as Teclistamab–Daratumumab offer a complementary strategy, one that combines accessibility, scalability, and sustained disease control. Monthly dosing after the initial treatment phase further supports feasibility in community oncology settings.

Clinical Implications

The MajesTEC-3 trial establishes Teclistamab plus Daratumumab as a highly effective immunotherapy-based option for patients with early relapsed multiple myeloma, delivering unprecedented Progression-Free Survival and deep molecular responses without the logistical barriers of cellular therapy. With appropriate supportive care and infection-prevention strategies, this regimen may meaningfully reset expectations for long-term disease control in a population historically characterized by inevitable relapse.

Conclusion

In patients with multiple myeloma who had received one to three prior lines of therapy, Teclistamab combined with Daratumumab significantly outperformed established Daratumumab-based regimens, offering durable disease control, deep responses, and a manageable safety profile. These findings position Teclistamab–Daratumumab as a potential new standard in earlier-line Relapsed or Refractory Multiple Myeloma, and signal continued progress toward prolonged survival in this traditionally incurable disease.

Teclistamab plus Daratumumab in Relapsed or Refractory Multiple Myeloma. Costa LJ,  Bahlis NJ, Perrot A, et al. for the MajesTEC-3 Trial Investigators. N Engl J Med 2026;394:739-752.

Adjuvant Immunotherapy Improves Outcomes in Stage III dMMR Colon Cancer: Results from the ATOMIC Trial

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SUMMARY: Colorectal cancer (CRC) is the third most common cancer diagnosed in both men and women in the United States. The American Cancer Society estimates that approximately 154,270 new cases of CRC will be diagnosed in the United States in 2025 and about 52,900 patients will die of the disease. The lifetime risk of developing CRC is about 1 in 23. The majority of CRC cases (about 75 %) are sporadic whereas the remaining 25 % of the patients have a family history of the disease. Only 5-6 % of patients with CRC with a family history background are due to inherited mutations in major CRC genes, while the rest are the result of accumulation of both genetic mutations and epigenetic modifications of several genes. Colorectal cancer is a heterogeneous disease classified by its genetics, and even though the diagnosis of CRC in the US is dropping among people 65 years and older, the incidence has been rising in the younger age groups, with 12% of CRC cases diagnosed in people under age 50.

It is estimated that 25% of patients diagnosed with Stage III disease have positive regional lymph nodes. These patients often receive 6 months of fluoropyrimidine-based adjuvant chemotherapy. The DNA MisMatchRepair (MMR) system is responsible for molecular surveillance and works as an editing tool that identifies errors within the microsatellite regions of DNA and removes them. Approximately 10% to 15% of nonmetastatic CRCs exhibit deficient mismatch repair (dMMR), accounting for an estimated 330,000 cases annually worldwide. Majority of dMMR tumors are sporadic, although some are associated with germline variants in genes that cause Hereditary Nonpolyposis Colon Cancer (HNPCC) or Lynch syndrome. These dMMR tumors are often seen in women, more likely to arise in the right side of the colon, and tend to grow large before they metastasize. Defective MMR system leads to MSI (Micro Satellite Instability) and hypermutation, with the expression of tumor-specific neoantigens at the surface of cancer cells, triggering an enhanced antitumor immune response. These tumors respond poorly to Fluoropyrimidine-based chemotherapy alone, especially in the adjuvant setting. While immune checkpoint inhibitors are approved for dMMR colorectal cancer in the metastatic setting, their benefit in earlier stages, particularly post-resection, had not been previously established in a prospective trial.

Atezolizumab (TECENTRIQ®) is an anti PD-L1 monoclonal antibody, designed to directly bind to PD-L1 expressed on tumor cells and tumor-infiltrating immune cells, thereby blocking its interactions with PD-1 and B7.1 receptors expressed on activated T cells. PD-L1 inhibition may prevent T-cell deactivation and further enable the activation of T cells.

The Phase 3 ATOMIC trial (NCT02912559), sponsored by the National Cancer Institute and conducted across multiple centers including NCTN sites and the German AIO group investigated whether the addition of Atezolizumab, a PD-L1 checkpoint inhibitor, to standard adjuvant chemotherapy could improve Disease-Free Survival (DFS) in patients with resected Stage III dMMR colon adenocarcinoma.

Study Design and Population
The trial enrolled 712 patients with surgically resected Stage III colon cancer confirmed to have dMMR. Eligibility included patients aged 12 years and older (one pediatric patient was enrolled). MMR status was initially determined locally by immunohistochemistry and subsequently confirmed centrally. Participants were randomized 1:1 to receive:

  • Control arm: mFOLFOX6 (5-Fluorouracil, Leucovorin, and Oxaliplatin) for 6 months (N=357)
  • Experimental arm: mFOLFOX6 plus Atezolizumab (840 mg IV every 2 weeks) for 6 months, followed by maintenance Atezolizumab monotherapy for an additional 6 months (N=355)

Median patient age was 64 yr. 55.1% were female, 84% of tumors were proximal, 46% were clinical low risk (T1-3N1) and 54% were high risk (T4 and/or N2). Stratification was based on nodal status (N1/N1c vs N2), tumor depth (T1-T3 vs T4), and tumor location (proximal vs distal colon). The Primary endpoint was Disease-Free Survival (DFS). Secondary endpoints included Overall Survival (OS) and Adverse Event (AE) profile.

Results and Efficacy
After a median follow-up of 40.9 months, the Primary endpoint of DFS was significantly improved in the Atezolizumab arm. The 3-year DFS was 86.3% in the combination arm vs 76.2% in the mFOLFOX6-only arm (Hazard Ratio (HR)=0.50; P<0.001, crossing the prespecified efficacy boundary. This represents a 50% relative reduction in the risk of recurrence or death with the addition of Atezolizumab. Importantly, the benefit was consistent across predefined subgroups, including patients over 70 years old and those with both low and high-risk disease (based on T and N-stage). Tumor location, patient sex, and race did not impact the observed treatment benefit.

Safety and Tolerability
Grade 3 or more treatment-related adverse events occurred in 84.1% of patients receiving Atezolizumab plus chemotherapy, compared to 71.9% in those receiving chemotherapy alone. Although the addition of Atezolizumab resulted in a modest increase in toxicity, the side effect profile was consistent with prior experience with checkpoint inhibitors and considered manageable.

Clinical Implications
The ATOMIC trial is the first large, prospective, randomized Phase 3 study to demonstrate a clear benefit from adding immunotherapy to adjuvant chemotherapy in Stage III dMMR colon cancer. As highlighted by the investigators, current adjuvant treatment recommendations for dMMR tumors have historically been extrapolated from studies in mismatch repair–proficient populations or based on retrospective analyses. The robust DFS improvement observed here provides definitive evidence supporting a new treatment paradigm for this molecularly defined subgroup.

There was no significant difference in Overall Survival noted at this first analysis at a median follow-up of 40.9 months, and longer follow-up is required for mature estimates. Future OS analyses may be complicated by the use of subsequent checkpoint inhibitors in patients who recur. The researchers emphasized the clinical relevance of these findings, noting their applicability to both sporadic dMMR cancers and Lynch syndrome associated tumors.

Future Directions
The ATOMIC trial sets a new benchmark for adjuvant therapy in dMMR colon cancer. However, important questions remain. Chief among them is the optimal duration of immunotherapy in this setting. Atezolizumab was administered for nearly a year, including maintenance. Ongoing research should clarify whether such prolonged treatment is necessary or if shorter regimens could maintain efficacy while reducing toxicity.

Moreover, while this study confirms benefit in the postoperative setting, parallel efforts are warranted to evaluate checkpoint inhibition in the neoadjuvant context. Encouraging responses such as those seen in small studies of neoadjuvant immunotherapy in dMMR rectal cancer highlight the need to explore earlier immunotherapeutic intervention in colon cancer as well.

Conclusion
The ATOMIC trial provides compelling evidence that incorporating Atezolizumab into adjuvant therapy improves Disease-free survival in patients with Stage III dMMR colon cancer, marking a major advancement in the management of this biologically distinct subset. Given these results, the combination of Atezolizumab and mFOLFOX6 should be considered the new standard of care in this setting. This trial also exemplifies the power of cooperative group studies in driving progress for biomarker-defined subsets within common malignancies.

Atezolizumab plus FOLFOX for Stage III Mismatch Repair–Deficient Colon Cancer. Sinicrope F, Ou F-S, Arnold D, et al. N Engl J Med 2026;394:1155-1166.