Abstract

SummaryBackgroundTwo radiotherapy fractionation schedules are used to treat locally advanced bladder cancer: 64 Gy in 32 fractions over 6·5 weeks and a hypofractionated schedule of 55 Gy in 20 fractions over 4 weeks. Long-term outcomes of these schedules in several cohort studies and case series suggest that response, survival, and toxicity are similar, but no direct comparison has been published. The present study aimed to assess the non-inferiority of 55 Gy in 20 fractions to 64 Gy in 32 fractions in terms of invasive locoregional control and late toxicity in patients with locally advanced bladder cancer.MethodsWe did a meta-analysis of individual patient data from patients (age ≥18 years) with locally advanced bladder cancer (T1G3 [high-grade non-muscle invasive] or T2–T4, N0M0) enrolled in two multicentre, randomised, controlled, phase 3 trials done in the UK: BC2001 (NCT00024349; assessing addition of chemotherapy to radiotherapy) and BCON (NCT00033436; assessing hypoxia-modifying therapy combined with radiotherapy). In each trial, the fractionation schedule was chosen according to local standard practice. Co-primary endpoints were invasive locoregional control (non-inferiority margin hazard ratio [HR]=1·25); and late bladder or rectum toxicity, assessed with the Late Effects Normal Tissue Task Force-Subjective, Objective, Management, Analytic tool (non-inferiority margin for absolute risk difference [RD]=10%). If non-inferiority was met for invasive locoregional control, superiority could be considered if the 95% CI for the treatment effect excluded the null effect (HR=1). One-stage individual patient data meta-analysis models for the time-to-event and binary outcomes were used, accounting for trial differences, within-centre correlation, randomised treatment received, baseline variable imbalances, and potential confounding from relevant prognostic factors.Findings782 patients with known fractionation schedules (456 from the BC2001 trial and 326 from the BCON trial; 376 (48%) received 64 Gy in 32 fractions and 406 (52%) received 55 Gy in 20 fractions) were included in our meta-analysis. Median follow-up was 120 months (IQR 99–159). Patients who received 55 Gy in 20 fractions had a lower risk of invasive locoregional recurrence than those who received 64 Gy in 32 fractions (adjusted HR 0·71 [95% CI 0·52–0·96]). Both schedules had similar toxicity profiles (adjusted RD −3·37% [95% CI −11·85 to 5·10]).InterpretationA hypofractionated schedule of 55 Gy in 20 fractions is non-inferior to 64 Gy in 32 fractions with regard to both invasive locoregional control and toxicity, and is superior with regard to invasive locoregional control. 55 Gy in 20 fractions should be adopted as a standard of care for bladder preservation in patients with locally advanced bladder cancer.FundingCancer Research UK.

Highlights

  • Bladder preservation therapy is an alternative to surgery for the management of locally advanced bladder cancer

  • Study design and participants We did a meta-analysis of individual patient data from patients with invasive bladder cancer enrolled in the multicentre, randomised, controlled, phase 3 trials BC20013,5 and BCON.[1]

  • We explored the fractionation effect within trials and in patients who received radiotherapy alone for invasive locoregional control, overall survival, and toxicity to assess robustness of results; adjusted HR (aHR) was the output with adjustment for the same factors as in the primary analyses

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Summary

Introduction

Bladder preservation therapy is an alternative to surgery for the management of locally advanced bladder cancer. This strategy comprises pretreatment staging with transurethral resection of the tumour and crosssectional imaging, followed by radiotherapy with or without a radiosensitiser. Combining radiotherapy with a radiosensitiser gives similar rates of disease-specific survival and overall survival (about 50% at 5 years for both endpoints) compared with surgery.[1,2,3,4] The two largest phase 3, randomised, controlled trials of bladder preservation showed benefit in terms of locoregional disease-free survival (the BC2001 trial3,5) and overall survival (BCON1) with use of chemotherapy (BC2001) or hypoxia-modifying therapy (BCON) concurrent with radiotherapy, compared with radiotherapy alo

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