Sasanlimab in combination with bacillus Calmette-Guérin (BCG) in BCG-naive in BCG-naive, high-risk non–muscle-invasive bladder cancer (NMIBC): Patient-reported outcomes (PROs) from CREST.
Abstract
4610 Background: Sasanlimab with BCG (induction [IND] + maintenance [MNT]) significantly improved investigator-assessed EFS vs BCG (IND + MNT) and had a manageable safety profile in patients (pts) with BCG-naive, high-risk NMIBC in the phase 3 CREST study primary analysis. We report PRO data not previously presented from CREST for Arms A and C assessing the impact of sasanlimab with BCG on QOL. Methods: Eligible pts were randomized 1:1:1 to receive sasanlimab with BCG (IND + MNT; Arm A), sasanlimab with BCG (IND; Arm B), or BCG (IND + MNT; Arm C). PROs were secondary endpoints and not included in the testing hierarchy. PROs were assessed prior to first dose (baseline [BL]), and at scheduled visits until an event or end of treatment (every 4 wk until Wk 28, every 12 wk until Wk 100) and at disease follow-up using the EORTC QLQ-C30 and QLQ-NMIBC24. Longitudinal mixed effect-model analyses were used to assess change from BL in the EORTC QLQ-C30 and NMIBC24 items. Results: At data cutoff (Dec 2, 2024), 695/703 pts randomized to Arms A (n = 348) and C (n = 347) had a BL score and ≥1 post-BL score. Completion rates were > 84% for all visits through the end-of-treatment visit (Cycle 25). QLQ-C30 Global Health Score QOL scores were numerically similar between arms (mean difference: −2.345; 95% CI: −4.058, −0.632; P = 0.007). No clinically meaningful differences (≥10-point change; Osoba et al. JCO 1998) were observed across urinary symptoms (NMIBC24; mean difference: 0.851; 95% CI: −1.030 , 2.731; P = 0.375), intravesical treatment issues (NMIBC24; mean difference: 1.271; 95% CI: −0.587, 3.130; P = 0.180), and EORTC QLQ-C30 items (Table) between arms, except in a small sample for female sexual problems (NMIBC24; mean difference: 18.502; 95% CI: 6.228, 30.775; P = 0.007). Results were statistically significant but not clinically meaningful. Conclusions: PROs from CREST showed QOL was maintained when combining sasanlimab with BCG vs BCG (both IND + MNT). These results can help inform the benefit-risk assessment of CREST. Clinical trial information: NCT04165317 . Arm AEstimated mean (95% CI)n=348 Arm CEstimated mean (95% CI)n=347 Estimated mean difference (95% CI) P value Physical functioning −2.485(−3.493, −1.477) −0.261(−1.272, 0.750) −2.224(−3.651, −0.796) 0.002 Role functioning −4.836(−6.187, −3.484) -0.910(−2.265, 0.445) −3.926(−5.840, −2.012) 0.000 Emotional functioning 0.074(−1.046, 1.194) 2.071(0.948, 3.194) −1.997(−3.583, −0.411) 0.014 Cognitive functioning −2.137(−3.174, −1.101) −0.832(−1.872, 0.208) −1.305(−2.774, 0.163) 0.081 Social functioning −3.863(−5.111, −2.615) −0.415(−1.666, 0.836) −3.448(−5.215, −1.681) 0.000 Fatigue 4.881(3.488, 6.274) 1.211(−0.185, 2.607) 3.670(1.698, 5.642) 0.000 Nausea and vomiting 0.908(0.473, 1.343) 0.545(0.108, 0.982) 0.363(−0.253, 0.980) 0.248 Pain 2.784(1.519, 4.048) −0.174(−1.443, 1.095) 2.958(1.166, 4.749) 0.001
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (17)
Jens Bedke
Eva Mayr-Stihl Cancer Center, Klinikum Stuttgart, Stuttgart, Germany
Neal D. Shore
START Carolinas/Carolina Urologic Research Center, Myrtle Beach, SC
Thomas Powles
Department of Medical Oncology Barts Cancer Institute Queen Mary University of London London UK
Matthew D. Galsky
Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai
Joan Palou
Department of Urology, Fundació Puigvert, Universitat Autònoma de Barcelona, Barcelona, Spain
Daniel R. Saltzstein
Urology San Antonio, San Antonio, TX
Félix Guerrero-Ramos
Motonobu Nakamura
Department of Urology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan
Tilman Todenhöfer
Studienpraxis Urologie, Nürtingen, Germany
Raj Satkunasivam
Peter Colin Black
Vancouver Prostate Center, University of British Columbia, Vancouver, BC, Canada
Julia Brinkmann
Pfizer Pharma GmbH, Berlin, Germany
Jane Chang
Pfizer Inc., New York, NY
Anthony Eccleston
Pfizer Ltd, Tadworth, United Kingdom
Arlene Reisman
Pfizer Inc., New York, NY
Jennifer Vermette
Pfizer, Inc., Cambridge, MA
Gary D. Steinberg
Rush University Medical Center, Chicago, IL