BCG plus mitomycin did not improve disease-free survival versus BCG alone in high-risk non-muscle-invasive bladder cancer patients
This randomized Phase 3 trial included 501 patients with BCG-naive non-muscle-invasive bladder cancer, specifically high-grade pTa or any grade pT1 lesions, where concurrent carcinoma in situ was allowed. The setting was not reported. Participants were randomized to receive either BCG plus mitomycin or BCG alone.
The primary outcome was disease-free survival (DFS). The 2-year DFS rate was 75% for the BCG plus mitomycin group versus 71% for the BCG alone group. The hazard ratio was 0.87 with a 95% confidence interval of 0.65-1.16 and a p-value of 0.3. The difference was not statistically significant, indicating the combination was not superior.
Secondary outcomes included complete response at 3 months, recurrence, progression, and deaths from any cause. Complete response rates were 214 versus 210. Recurrence events were 79 versus 86. Progression events were 28 versus 44. Deaths were 26 versus 23. The combination arm required 4033 instillations versus 3383 for BCG alone. Total BCG doses were 2056 versus 3383, with a median of nine versus 16 doses respectively.
Safety analysis showed Grade 3-5 adverse events occurred in 43 assigned patients in the BCG plus mitomycin group versus 37 in the BCG alone group. Fewer treatment discontinuations were observed for the combination therapy. The study did not report serious adverse events or overall tolerability. No funding or conflicts were reported.
The findings support considering BCG plus mitomycin as a pragmatic alternative to BCG alone. This approach requires 39% fewer doses of BCG and fewer treatment discontinuations. These factors could help mitigate the global shortage of BCG while maintaining comparable disease-free survival.