Chemoradiotherapy in Muscle-invasive Bladder Cancer: 10-yr Follow-up of the Phase 3 Randomised Controlled BC2001 Trial.


Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
09 2022
Historique:
received: 06 01 2022
revised: 21 03 2022
accepted: 17 04 2022
pubmed: 17 5 2022
medline: 17 8 2022
entrez: 16 5 2022
Statut: ppublish

Résumé

BC2001, the largest randomised trial of bladder-sparing treatment for muscle-invasive bladder cancer (MIBC), demonstrated improvement in locoregional control by adding fluorouracil and mitomycin C to radiotherapy (James ND, Hussain SA, Hall E, et al. Radiotherapy with or without chemotherapy in muscle-invasive bladder cancer. N Engl J Med 2012;366:1477-88). There are limited data on long-term recurrence risk. To determine whether benefit of adding chemotherapy to radiotherapy for MIBC is maintained in the long term. A phase 3 randomised controlled 2 × 2 factorial trial was conducted. Between 2001 and 2008, 458 patients with T2-T4a N0M0 MIBC were enrolled; 360 were randomised to radiotherapy (178) or chemoradiotherapy (182), and 218 were randomised to standard whole-bladder radiotherapy (108) or reduced high-dose-volume radiotherapy (111). The median follow-up time was 9.9 yr. The trial is registered (ISRCTN68324339). Radiotherapy: 55 Gy in 20 fractions over 4 wk or 64 Gy in 32 fractions over 6.5 wk; concurrent chemotherapy: 5-fluorouracil and mitomycin C. Locoregional control (primary endpoint), invasive locoregional control, toxicity, rate of salvage cystectomy, disease-free survival (DFS), metastasis-free survival (MFS), bladder cancer-specific survival (BCSS), and overall survival. Cox regression was used. The analysis of efficacy outcomes was by intention to treat. Chemoradiotherapy improved locoregional control (hazard ratio [HR] 0.61 [95% confidence interval {CI} 0.43-0.86], p = 0.004) and invasive locoregional control (HR 0.55 [95% CI 0.36-0.84], p = 0.006). This benefit translated, albeit nonsignificantly, for disease-related outcomes: DFS (HR 0.78 [95% CI 0.60-1.02], p = 0.069), MFS (HR 0.78, [95% CI 0.58-1.05], p = 0.089), overall survival (HR = 0.88 [95% CI 0.69-1.13], p = 0.3), and BCSS (HR 0.79 [95% CI 0.59-1.06], p = 0.11). The 5-yr cystectomy rate was 14% (95% CI 9-21%) with chemoradiotherapy versus 22% (95% CI 16-31%) with radiotherapy alone (HR 0.54, [95% CI 0.31-0.95], p = 0.034). No differences were seen between standard and reduced high-dose-volume radiotherapy. Long-term findings confirm the benefit of adding concomitant 5-fluorouracil and mitomycin C to radiotherapy for MIBC. We looked at long-term outcomes of a phase 3 clinical trial testing radiotherapy with or without chemotherapy for patients with invasive bladder cancer. We concluded that the benefit of adding chemotherapy to radiotherapy was maintained over 10 yr.

Sections du résumé

BACKGROUND
BC2001, the largest randomised trial of bladder-sparing treatment for muscle-invasive bladder cancer (MIBC), demonstrated improvement in locoregional control by adding fluorouracil and mitomycin C to radiotherapy (James ND, Hussain SA, Hall E, et al. Radiotherapy with or without chemotherapy in muscle-invasive bladder cancer. N Engl J Med 2012;366:1477-88). There are limited data on long-term recurrence risk.
OBJECTIVE
To determine whether benefit of adding chemotherapy to radiotherapy for MIBC is maintained in the long term.
DESIGN, SETTING, AND PARTICIPANTS
A phase 3 randomised controlled 2 × 2 factorial trial was conducted. Between 2001 and 2008, 458 patients with T2-T4a N0M0 MIBC were enrolled; 360 were randomised to radiotherapy (178) or chemoradiotherapy (182), and 218 were randomised to standard whole-bladder radiotherapy (108) or reduced high-dose-volume radiotherapy (111). The median follow-up time was 9.9 yr. The trial is registered (ISRCTN68324339).
INTERVENTION
Radiotherapy: 55 Gy in 20 fractions over 4 wk or 64 Gy in 32 fractions over 6.5 wk; concurrent chemotherapy: 5-fluorouracil and mitomycin C.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS
Locoregional control (primary endpoint), invasive locoregional control, toxicity, rate of salvage cystectomy, disease-free survival (DFS), metastasis-free survival (MFS), bladder cancer-specific survival (BCSS), and overall survival. Cox regression was used. The analysis of efficacy outcomes was by intention to treat.
RESULTS AND LIMITATIONS
Chemoradiotherapy improved locoregional control (hazard ratio [HR] 0.61 [95% confidence interval {CI} 0.43-0.86], p = 0.004) and invasive locoregional control (HR 0.55 [95% CI 0.36-0.84], p = 0.006). This benefit translated, albeit nonsignificantly, for disease-related outcomes: DFS (HR 0.78 [95% CI 0.60-1.02], p = 0.069), MFS (HR 0.78, [95% CI 0.58-1.05], p = 0.089), overall survival (HR = 0.88 [95% CI 0.69-1.13], p = 0.3), and BCSS (HR 0.79 [95% CI 0.59-1.06], p = 0.11). The 5-yr cystectomy rate was 14% (95% CI 9-21%) with chemoradiotherapy versus 22% (95% CI 16-31%) with radiotherapy alone (HR 0.54, [95% CI 0.31-0.95], p = 0.034). No differences were seen between standard and reduced high-dose-volume radiotherapy.
CONCLUSIONS
Long-term findings confirm the benefit of adding concomitant 5-fluorouracil and mitomycin C to radiotherapy for MIBC.
PATIENT SUMMARY
We looked at long-term outcomes of a phase 3 clinical trial testing radiotherapy with or without chemotherapy for patients with invasive bladder cancer. We concluded that the benefit of adding chemotherapy to radiotherapy was maintained over 10 yr.

Identifiants

pubmed: 35577644
pii: S0302-2838(22)02265-5
doi: 10.1016/j.eururo.2022.04.017
pii:
doi:

Substances chimiques

Mitomycin 50SG953SK6
Fluorouracil U3P01618RT

Banques de données

ISRCTN
['ISRCTN68324339']

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

273-279

Subventions

Organisme : Department of Health
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C547/A2606
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C9764/A9904
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C1491/A9895
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C1491/A15955
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C1491/A25351
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Emma Hall (E)

The Institute of Cancer Research, London, UK. Electronic address: Emma.Hall@icr.ac.uk.

Syed A Hussain (SA)

University of Sheffield & Sheffield Teaching Hospitals, Sheffield, UK.

Nuria Porta (N)

The Institute of Cancer Research, London, UK.

Rebecca Lewis (R)

The Institute of Cancer Research, London, UK.

Malcolm Crundwell (M)

Royal Devon & Exeter NHS Foundation Trust, Exeter, UK.

Peter Jenkins (P)

Gloucestershire Oncology Centre, Cheltenham Hospital, Cheltenham, UK.

Christine Rawlings (C)

Torbay and South Devon NHS Foundation Trust, Torquay, UK.

Jean Tremlett (J)

Brighton and Sussex University Hospitals NHS Trust, Brighton, UK.

Thiagarajan Sreenivasan (T)

United Lincolnshire Hospitals NHS Trust, Lincolnshire, UK.

Jan Wallace (J)

NHS Greater Glasgow and Clyde, Glasgow, Scotland.

Isabel Syndikus (I)

Clatterbridge Centre NHS Trust, Wirral, UK.

Denise Sheehan (D)

Royal Devon & Exeter NHS Foundation Trust, Exeter, UK.

Anna Lydon (A)

Torbay and South Devon NHS Foundation Trust, Torquay, UK.

Robert Huddart (R)

The Institute of Cancer Research, London, UK; The Royal Marsden NHS Foundation Trust, London, UK.

Nicholas James (N)

The Institute of Cancer Research, London, UK; The Royal Marsden NHS Foundation Trust, London, UK.

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Classifications MeSH