AETOSWire: Multiple New Analyses Reinforce the Role of BAVENCIO® (avelumab) First-Line Maintenance as a Standard of Care in Patients with Locally Advanced or Metastatic Urothelial Carcinoma

DARMSTADT, Germany

Not intended for UK-, US- or Canada-based media

Abstracts to be presented at the 2024 American Society of Clinical Oncology’s annual Genitourinary Cancers Symposium provide insights into treatment selection and sequencing, as well as quality of life

Latest real-world data show median overall survival (OS) from start of first-line chemotherapy of about 30 months for patients treated with the JAVELIN Bladder regimen without progression following chemotherapy

Exploratory analyses suggest that in patients who received ADC therapy after the JAVELIN Bladder regimen, median OS from start of first-line chemotherapy reached 40 months in real-world study

(BUSINESS WIRE)--Merck, a leading science and technology company, today announced new real-world data that continue to reinforce the JAVELIN Bladder regimen of first-line platinum-based chemotherapy followed by BAVENCIO® (avelumab) maintenance as a standard of care for eligible patients with locally advanced or metastatic urothelial carcinoma (UC) who do not progress on first-line chemotherapy. Data include real-world studies that confirm median overall survival (OS) of approximately 30 months in patients without progression after first-line chemotherapy. Additional analyses offer insights into treatment sequencing outcomes in the real world, with the first analysis of OS by next-line treatment, including in patients who received an antibody-drug conjugate (ADC) such as enfortumab vedotin after the JAVELIN Bladder regimen. These and other analyses will be presented at the 2024 American Society of Clinical Oncology’s annual Genitourinary Cancers Symposium, January 25-27, in San Francisco.

“Avelumab in the first-line maintenance setting is a standard of care for patients with locally advanced or metastatic bladder cancer, with a well-established efficacy and safety profile and supported by years of real-world experience. These new analyses add to the large body of evidence, showing avelumab maintenance treatment can help extend overall survival while potentially providing a favorable quality of life,” said Philippe Barthélémy, Institut de Cancérologie Strasbourg Europe, France. “The ongoing exploratory analysis of the real-world AVENANCE study may provide new insights indicating that the initial use of the JAVELIN Bladder regimen, followed by a second-line antibody-drug conjugate treatment like enfortumab vedotin, could greatly enhance overall survival outcomes for patients. These findings underscore the importance of strategic treatment sequencing in optimizing patient outcomes.”

Real-world insights into treatment sequencing following the JAVELIN Bladder regimen

Real-world data and analyses by subsequent treatment from the ongoing, real-world, ambispective (retrospective and prospective) AVENANCE study in France continue to support the use of BAVENCIO first-line maintenance while also demonstrating the impact of subsequent therapies once BAVENCIO treatment is discontinued. With a median follow-up since initiation of BAVENCIO of 26.3 months, median OS from the start of BAVENCIO maintenance was 21.3 months (n=595; 95% CI, 17.6 to 24.6) in patients who did not progress on first-line platinum-based chemotherapy and received BAVENCIO first-line maintenance. In an exploratory analysis, median OS from the start of platinum-based chemotherapy was 26.5 months (95% CI, 23.4 to 30.1). Subgroup analyses evaluated outcomes in the 330 patients who received second-line therapy, with median OS from the start of BAVENCIO maintenance of 31.3 months (95% CI, 29.1 to NE) in the 62 patients who received a second-line ADC (enfortumab vedotin: n=56; sacituzumab govitecan: n=6) and 16.7 months (95% CI, 13.6 to 22.8) in the 81 patients who received second-line platinum-based chemotherapy. Among the patients who received a second-line ADC, median OS measured from the start of chemotherapy was 40.8 months (95% CI, 32.6 to 42.1) in the exploratory analysis.

Long-term efficacy with the JAVELIN Bladder regimen in the real world

Real-world analyses of BAVENCIO first-line maintenance show median OS from the start of chemotherapy of at least 30 months in this population of patients who do not progress on first-line platinum-based chemotherapy, consistent with previously reported results of a long-term exploratory analysis from JAVELIN Bladder 100.

PATRIOT-II U.S. Real-World Study: The observational, retrospective PATRIOT-II study analyzed medical records from 160 U.S. patients, with median follow-up from the start of BAVENCIO maintenance of 16 months (range, 11-21 months). Patients who received BAVENCIO first-line maintenance treatment following chemotherapy achieved a median OS of 30.5 months measured from the start of first-line chemotherapy (95% CI, 23.4 to 37.6). Median OS was 24.4 months measured from the start of maintenance treatment (95% CI, 20.4 to 28.4).

READY CUP Italy Real-World Study: The prospective, noninterventional compassionate use program (CUP) provided Italian patients with locally advanced or metastatic UC early access to BAVENCIO first-line maintenance before reimbursement. With median follow-up of 20.3 months (95% CI, 19.8 to 20.9), median OS measured from start of first-line chemotherapy was 30.9 months (95% CI, 25.7 to NE) in this population without progression after chemotherapy. Median OS from the start of maintenance treatment was 26.2 months (95% CI, 20.0 to NE).

Analyses of quality of life and efficacy in JAVELIN Bladder 100

Patient-Reported Outcomes from JAVELIN Bladder 100: This post-hoc analysis assessed long-term patient-reported outcomes (PRO) data using the National Comprehensive Cancer Network/Functional Assessment of Cancer Therapy Bladder Symptom Index-18 (FBlSI-18) and EuroQoL 5 Dimensions 5 Levels (EQ-5D-5L).An analysis of scores over all cycles prior to end of BAVENCIO treatment PRO patient-reported outcomes scores were BAVENCIO treatment:, with a -2.15 mean change from baseline of -2.15 (95% CI, -3.25 to -1.04) in the FBISI-18 score and -.07 (95% CI, -.09 to -.05) in the EQ-5D-5L index score. In patients with 12 months or more of BAVENCIO treatment, there was a 1.28 mean change from baseline (95% CI, .08 to 2.49) in the FBISI-18 score and a -.02 mean change in the EQ-5D-5L index score further supporting the use of the JAVELIN Bladder regimen in eligible patients with advanced UC until progression or unacceptable toxicity.

High BMI Subgroup Analysis from JAVELIN Bladder 100: This exploratory subgroup analysis (n=122) showed the efficacy and safety of BAVENCIO maintenance treatment in patients with a high body mass index (BMI; ≥30 kg/m2)—a key patient population given that high BMI is a risk factor for bladder cancer, and 25% of the world’s population is anticipated to have a high BMI by 2035. In patients with high BMI at baseline, median OS for patients receiving BAVENCIO maintenance therapy plus BSC was 20.8 months from the start of maintenance treatment (95% CI, 16.9 to 34.4), compared with 12.7 months (95% CI, 8.1 to 26.6 months) for BSC alone (HR: 0.77; 95% CI, 0.49 to 1.21). Long-term safety for patients with high BMI was consistent with results from the overall population.

“The JAVELIN Bladder 100 study helped transform the standard of care for patients with advanced bladder cancer, at a time when there had been few advancements in decades. By continuing to share new research on BAVENCIO, including data on health-related quality of life, key patient populations, and treatment sequencing, we can further support clinicians in making informed treatment decisions for each individual patient,” said Tamas Sütö, MD, PhD, Senior Vice President & Head of Medical Unit Oncology, Merck.

All company presentations in urothelial cancer at ASCO GU 2024 are listed below.

Title

Lead Author, Abstract # and Session Details (all times PT)

Real-world treatment patterns (tx) and clinical outcomes in patients (pts) with locally advanced or metastatic urothelial carcinoma (la/mUC) in Germany: Results of a retrospective observational study (CONVINCE)

S. Machtens

Abstract #551