In JAVELIN Bladder 100, avelumab first-line maintenance plus best supportive care (BSC) significantly prolonged overall survival versus BSC alone, with no detrimental impact on quality of life (QOL), in patients with advanced urothelial carcinoma without progression following first-line platinum-based chemotherapy.
We report long-term analyses of patient-reported outcomes (PROs) in patients treated with avelumab (any duration or ≥12 mo) and a post hoc analysis comparing quality-adjusted time without symptoms or toxicity (Q-TWiST) between arms.
PROs were assessed using National Comprehensive Cancer Network/Functional Assessment of Cancer Therapy Bladder Symptom Index-18 (FBlSI-18) and EuroQol 5-level EQ-5D (EQ-5D-5L). Q-TWiST was calculated as the utility-weighted sum of mean time in three health states: time with all-cause grade 3/4 toxicity prior to progression, time without grade 3/4 toxicity or symptoms of progression, and time after progression.
In the overall avelumab plus BSC arm (n = 350) and the subgroup treated for ≥12 mo (n = 118), completion rates for PRO assessments during treatment were >80%. FBlSI-18 total and EQ-5D-5L index scores remained stable throughout 24 mo of treatment, with no clinically important changes from baseline. The mean Q-TWiST was 18.46 mo with avelumab plus BSC versus 15.13 mo with BSC alone (22% relative improvement). Limitations include open-label trial design and small patient numbers at later cycles.
Patients receiving avelumab had preserved health-related QOL and control of cancer-related symptoms with manageable toxicity, further supporting avelumab first-line maintenance as the recommended treatment for advanced urothelial carcinoma not progressed after platinum-based chemotherapy.
European urology oncology. 2025 May 02 [Epub ahead of print]
Petros Grivas, Jeanny B Aragon-Ching, Joaquim Bellmunt, Yohann Loriot, Miguel A Climent Duran, Srikala S Sridhar, Po-Jung Su, Se Hoon Park, Evgeny Kopyltsov, Yoshiaki Yamamoto, Natalia Jacob, Jason Hoffman, Karin Tyroller, Juliane Manitz, Mairead Kearney, Michael Schlichting, Thomas Powles
University of Washington, Fred Hutchinson Cancer Center, Seattle, WA, USA. Electronic address: ., Inova Schar Cancer Institute, Fairfax, VA, USA., Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA., Gustave Roussy, INSERMU981, Université Paris-Saclay, Villejuif, France., Instituto Valenciano de Oncología, Valencia, Spain., Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada., Division of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan; College of Medicine, Chang Gung University, Taoyuan, Taiwan., Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea., State Institution of Healthcare Regional Clinical Oncology Dispensary, Omsk, Russia., Yamaguchi University, Ube, Yamaguchi, Japan., Merck Healthcare KGaA, Darmstadt, Germany., EMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA., Experimental Cancer Medicine Centre, Barts Cancer Institute, Queen Mary University of London, St Bartholomew's Hospital, London, UK.
PubMed http://www.ncbi.nlm.nih.gov/pubmed/40318950