Avelumab First-Line Maintenance for Locally Advanced or Metastatic Urothelial Carcinoma: Results From the Real-World US PATRIOT-II Study
Year: 2024
Type: article
Study design: Observational Study
Abstract: INTRODUCTION: In JAVELIN Bladder 100, avelumab first-line maintenance (1LM) improved overall survival (OS) and progression-free survival (PFS) in patients with locally advanced/metastatic urothelial carcinoma (la/mUC) without progression following 1L platinum-based chemotherapy (PBC) versus best supportive care. PATRIOT-II describes real-world outcomes with avelumab 1LM. PATIENTS AND METHODS: This observational, retrospective study of avelumab 1LM in US community/academic centers used medical record data collected from avelumab initiation for ≥12 months to assess survival, safety, and healthcare resource utilization; analyses are descriptive. RESULTS: The study included 160 patients from 37 centers (median age, 70 years; 77% male). Avelumab 1LM was initiated at a median of 4 weeks (IQR 3-6) after PBC completion. Median follow-up from avelumab 1LM was 16 months (IQR 11-21). At study end, 19.4% of patients continued avelumab; 73.7% had discontinued due to progression, adverse events (AEs), or performance status deterioration. Median PFS and OS from avelumab initiation were 5.4 months (95% CI, 3.8-6.9) and 24.4 months (95% CI, 20.4-28.4), respectively. Grade ≥3 treatment-related AEs (TRAEs) occurred in 15 patients (9.4%); 35 (21.9%) had any-grade immune-related AEs, and 23 (14.3%) received high-dose systemic corticosteroids for AEs. Forty-four patients (27.5%) were hospitalized during the avelumab treatment period, of whom 13 (8.1%) were hospitalized due to TRAEs. Limitations of this study include a small sample size, potential selection bias, and missing/unknown data. CONCLUSION: These results align with the JAVELIN Bladder 100 clinical trial and other real-world studies, supporting avelumab 1LM use in patients with la/mUC without progression following 1L PBC.
Source: Clinical Genitourinary Cancer
Authors: Petros Grivas, Pedro Barata, Helen Moon, Shilpa Gupta, Thomas Hutson, Cora N. Sternberg, Jason R. Brown, Vaidehi Dave, Chad Downey, Alicia C. Shillington, Howard M. Katzenstein, Melissa Kirker, Sarah Hanson, Frank X. Liu, Valerie Morris, Abhijeet Bhanegaonkar, Guru P. Sonpavde
Institutions: University of Washington, Fred Hutch Cancer Center, University Hospitals Seidman Cancer Center, Kaiser Permanente, Kaiser Permanente Riverside Medical Center, Cleveland Clinic, Texas Oncology, Weill Cornell Medicine, University Hospitals of Cleveland, RTI Health Solutions, Epi-Q (United States), EMD Serono, Inc. (United States), Merck Healthcare KGaA, Darmstadt (Germany), Pfizer (United States), AdventHealth Orlando, AdventHealth
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $3,690
Funders: Amgen, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, AstraZeneca, Sanofi, Gilead Sciences, United Therapeutics Corporation, Sunovion, Merck KGaA, Exelixis, Clovis Oncology, Neurocrine Biosciences, Acceleron, Jounce Therapeutics, Mirati Therapeutics, Janssen Scientific Affairs, Incyte, Apollomics, Moderna, G1 Therapeutics, Seagen, Eisai, Astellas Pharma, Bavarian Nordic, Genentech, EMD Serono, Foundation Medicine
OpenAlex ID: W4403500663
