4.6 Article

Intravesical chemotherapy plus bacille Calmette-Guerin in non-muscle invasive bladder cancer: a systematic review with meta-analysis

期刊

BJU INTERNATIONAL
卷 111, 期 6, 页码 977-983

出版社

WILEY
DOI: 10.1111/j.1464-410X.2012.11390.x

关键词

urinary bladder neoplasm; BCG vaccine; mitomycin C; epirubicin; intravesical administration

资金

  1. Australian Government through Cancer Australia

向作者/读者索取更多资源

What's known on the subject? and What does the study add? Non-muscle-invasive bladder cancer has a significant recurrence and progression rate despite transurethral resection. The current standard of care to lower the risk of recurrence and progression is adjuvant BCG followed by maintenance BCG. Despite this, a significant number of patients experience recurrence and progress to invasive cancer. Several randomized trials have studied combination therapy (BCG with chemotherapy) to try to reduce the recurrence and progression rate. We performed a systematic review with meta-analysis and found that adjuvant BCG followed by maintenance therapy is the appropriate standard of care when compared with combination therapy. We conclude that further trials are warranted to test the effects of adding chemotherapy to BCG in patients with Ta or T1 disease, but not in those with Tis alone. Objective To determine if the combination of intravesical chemotherapy and maintenance bacille Calmette-Guerin (BCG), used in sequence, is superior to maintenance BCG alone in the treatment of non-muscle-invasive bladder cancer (NMIBC). Methods We searched biomedical literature databases for randomized controlled trials that compared sequential, intravesical chemotherapy added to maintenance BCG with maintenance BCG alone. Studies that did not use maintenance BCG were excluded. The meta-analysis was performed using the fixed effects model. Results Four trials were identified, including 801 patients. Adding chemotherapy to maintenance BCG did not result in a significant reduction in recurrence (relative risk [RR] 0.92; 95% confidence interval [CI] 0.791.09; P = 0.32) or progression (RR 0.88; 95% CI 0.611.27; P = 0.5). The risk of recurrence (RR 0.75; 95% CI 0.610.92; P = 0.006) and progression (RR 0.45; 95% CI 0.250.81; P = 0.007) were reduced when the single trial that included isolated Tis was excluded. Toxicity was similar for both groups. Conclusions Adjuvant therapy with induction BCG followed by maintenance BCG is the appropriate standard of care for patients with resected NMIBC at high risk of recurrence. Further trials are warranted to test the effects of adding chemotherapy to BCG in patients with Ta or T1 disease, but not in those with Tis alone.

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