Comparative outcomes of chemoradiotherapy regimens in muscle-invasive bladder cancer: A retrospective cohort study.
Abstract
738 Background: Bladder-preserving chemoradiotherapy (CRT) is an organ-sparing alternative to radical cystectomy for muscle-invasive bladder cancer (MIBC). This study compared outcomes and toxicity among three CRT regimens: weekly cisplatin, 5-fluorouracil plus mitomycin C (5-FU + MMC), and weekly low-dose gemcitabine. Methods: Patients with cT2–T4a N0-N1–N1 MIBC who underwent maximal TURBT followed by definitive CRT (median 64 Gy) were retrospectively analyzed. Primary endpoints were overall survival (OS) and disease-free survival (DFS). Analyses used Kaplan–Meier, Cox regression, and inverse probability of treatment weighting (IPTW). Results: Ninety-eight patients were included (median age 73; 79% male). Complete response occurred in 84% overall: 75% cisplatin, 84% 5-FU+MMC, 91% gemcitabine (p = 0.39). After 37 months’ follow-up, 5-year OS was 52% (p = 0.63), 3-year DFS 46% (p = 0.40). Distant relapse 50%; bladder-only 3%. Grade ≥3 toxicity 20% overall—22% cisplatin, 23% 5-FU+MMC, 13% gemcitabine (p = 0.58). Nodal disease predicted worse OS (HR 2.5, 95% CI 1.0–6.2; p = 0.04); regimen was not prognostic. IPTW confirmed results. Conclusions: Trimodality CRT achieved durable bladder preservation (~50% 5-year OS) with low local relapse. Efficacy was similar across regimens; gemcitabine showed lower toxicity. Distant relapse predominated, underscoring need for improved systemic therapy. Baseline characteristics, treatment response, survival, and toxicity by chemotherapy regimen. Parameter Cisplatin (n=32) 5-FU+MMC (n=34) Gemcitabine (n=32) p-value N1 disease (%) 28 15 10 0.01 Neoadjuvant chemotherapy (%) 28 12 15 0.10 Complete response (%) 81 85 88 0.38 3-year OS (%) 63 65 72 0.63 5-year OS (%) 50 52 55 0.62 3-year DFS (%) 44 47 48 0.40 Grade ≥3 toxicity (%) 22 21 12.5 0.25 Isolated bladder relapse (%) 3 3 3 0.95 Distant failures (%) 53 48 50 0.80 Comparative outcomes among patients treated with concurrent chemoradiotherapy (CTRT) using cisplatin-, 5-fluorouracil plus mitomycin-C (5-FU+MMC)-, or gemcitabine-based regimens. Percentages denote the proportion of patients per group. Complete response (CR) was defined radiologically and/or cystoscopically after CTRT. OS and DFS were measured from treatment start to death or recurrence. Grade ≥3 toxicity reflects clinically significant events retrospectively classified per CTCAE v5.0 where applicable. p-values were from chi-square or Fisher’s exact test; <0.05 was significant.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (6)
Bharath Bilidevalaya Gangadharaiah
Medical Oncology and Hematology, CancerCare Manitoba, University of Manitoba, Winnipeg, MB, Canada
Piotr Czaykowski
Medical Oncology and Hematology, University of Manitoba, CancerCare Manitoba, Winnipeg, MB, Canada
Hanbo Zhang
Medical Oncology and Hematology, University of Manitoba, CancerCare Manitoba, Winnipeg, MB, Canada
Joel Roger Gingerich
Medical Oncology and Hematology, University of Manitoba, CancerCare Manitoba, Winnipeg, MB, Canada
Bashir Bashir
Radiation Oncology, CancerCare Manitoba, University of Manitoba, Winnipeg, MB, Canada
Jeffrey Graham
Intermountain Medical Center, Salt Lake City, Utah, United States