Perioperative dose-dense methotrexate, vinblastine, doxorubicin, and cisplatin in muscle-invasive bladder cancer (VESPER): survival endpoints at 5 years in an open-label, randomised, phase 3 study.


Journal

The Lancet. Oncology
ISSN: 1474-5488
Titre abrégé: Lancet Oncol
Pays: England
ID NLM: 100957246

Informations de publication

Date de publication:
21 Dec 2023
Historique:
received: 08 06 2023
revised: 03 11 2023
accepted: 09 11 2023
medline: 25 12 2023
pubmed: 25 12 2023
entrez: 24 12 2023
Statut: aheadofprint

Résumé

The optimal perioperative chemotherapy for patients with muscle-invasive bladder cancer is not defined. The VESPER (French Genito-Urinary Tumor Group and French Association of Urology V05) trial reported improved 3-year progression-free survival with dose-dense methotrexate, vinblastine, doxorubicin and cisplatin (dd-MVAC) versus gemcitabine and cisplatin (GC) in patients who received neoadjuvant therapy, but not in the overall perioperative setting. In this Article, we report on the secondary endpoints of overall survival and time to death due to bladder cancer at 5-year follow-up. VESPER was an open-label, randomised, phase 3 trial done at 28 university hospitals or comprehensive cancer centres in France, in which adults (age ≤18 years and ≤80 years) with primary bladder cancer and histologically confirmed muscle-invasive urothelial carcinoma were randomly allocated (1:1; block size four) to treatment with dd-MVAC (every 2 weeks for a total of six cycles) or GC (every 3 weeks for a total of four cycles). Overall survival and time to death due to bladder cancer (presented as 5-year cumulative incidence of death due to bladder cancer) was analysed by intention to treat (ITT) in all randomly assigned patients. Overall survival was assessed by the Kaplan-Meier method with the treatment groups compared with log-rank test stratified for mode of administration of chemotherapy (neoadjuvant or adjuvant) and lymph node involvement. Time to death due to bladder cancer was analysed with an Aalen model for competing risks and a Fine and Gray regression model stratified for the same two covariates. Results were presented for the total perioperative population and for the neoadjuvant and adjuvant subgroups. The trial is registered with ClinicalTrials.gov, NCT01812369, and is complete. From Feb 25, 2013, to March 1, 2018, 500 patients were randomly assigned, of whom 493 were included in the final ITT population (245 [50%] in the GC group and 248 [50%] in the dd-MVAC group; 408 [83%] male and 85 [17%] female). 437 (89%) patients received neoadjuvant chemotherapy. Median follow-up was 5·3 years (IQR 5·1-5·4); 190 deaths at the 5-year cutoff were reported. In the perioperative setting (total ITT population), we found no evidence of association of overall survival at 5 years with dd-MVAC treatment versus GC treatment (64% [95% CI 58-70] vs 56% [50-63], stratified hazard ratio [HR Our results on overall survival at 5 years were in accordance with the primary endpoint analysis (3-year progression-free survival). We found no evidence of improved overall survival with dd-MVAC over GC in the perioperative setting, but the data support the use of six cycles of dd-MVAC over four cycles of GC in the neoadjuvant setting. These results should impact practice and future trials of immunotherapy in bladder cancer. French National Cancer Institute.

Sections du résumé

BACKGROUND BACKGROUND
The optimal perioperative chemotherapy for patients with muscle-invasive bladder cancer is not defined. The VESPER (French Genito-Urinary Tumor Group and French Association of Urology V05) trial reported improved 3-year progression-free survival with dose-dense methotrexate, vinblastine, doxorubicin and cisplatin (dd-MVAC) versus gemcitabine and cisplatin (GC) in patients who received neoadjuvant therapy, but not in the overall perioperative setting. In this Article, we report on the secondary endpoints of overall survival and time to death due to bladder cancer at 5-year follow-up.
METHODS METHODS
VESPER was an open-label, randomised, phase 3 trial done at 28 university hospitals or comprehensive cancer centres in France, in which adults (age ≤18 years and ≤80 years) with primary bladder cancer and histologically confirmed muscle-invasive urothelial carcinoma were randomly allocated (1:1; block size four) to treatment with dd-MVAC (every 2 weeks for a total of six cycles) or GC (every 3 weeks for a total of four cycles). Overall survival and time to death due to bladder cancer (presented as 5-year cumulative incidence of death due to bladder cancer) was analysed by intention to treat (ITT) in all randomly assigned patients. Overall survival was assessed by the Kaplan-Meier method with the treatment groups compared with log-rank test stratified for mode of administration of chemotherapy (neoadjuvant or adjuvant) and lymph node involvement. Time to death due to bladder cancer was analysed with an Aalen model for competing risks and a Fine and Gray regression model stratified for the same two covariates. Results were presented for the total perioperative population and for the neoadjuvant and adjuvant subgroups. The trial is registered with ClinicalTrials.gov, NCT01812369, and is complete.
FINDINGS RESULTS
From Feb 25, 2013, to March 1, 2018, 500 patients were randomly assigned, of whom 493 were included in the final ITT population (245 [50%] in the GC group and 248 [50%] in the dd-MVAC group; 408 [83%] male and 85 [17%] female). 437 (89%) patients received neoadjuvant chemotherapy. Median follow-up was 5·3 years (IQR 5·1-5·4); 190 deaths at the 5-year cutoff were reported. In the perioperative setting (total ITT population), we found no evidence of association of overall survival at 5 years with dd-MVAC treatment versus GC treatment (64% [95% CI 58-70] vs 56% [50-63], stratified hazard ratio [HR
INTERPRETATION CONCLUSIONS
Our results on overall survival at 5 years were in accordance with the primary endpoint analysis (3-year progression-free survival). We found no evidence of improved overall survival with dd-MVAC over GC in the perioperative setting, but the data support the use of six cycles of dd-MVAC over four cycles of GC in the neoadjuvant setting. These results should impact practice and future trials of immunotherapy in bladder cancer.
FUNDING BACKGROUND
French National Cancer Institute.

Identifiants

pubmed: 38142702
pii: S1470-2045(23)00587-9
doi: 10.1016/S1470-2045(23)00587-9
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT01812369']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Investigateurs

Géraldine Pignot (G)
Jean Philippe Fendler (JP)
Laurent Guy (L)
Grégory Verhoest (G)
Nicolas Mottet (N)
Arnaud Doerfler (A)
Sophie Abadie Lacourtoisie (S)
Abde Rahmene Azzouzi (AR)
Pierre Mongiat (P)
Lionnel Geoffrois (L)
Pascal Eschwege (P)
Frédéric DI Fiore (F)
Guilhem Roubaud (G)
Jean Luc Hoepffner (JL)
Philippe Barthelemy (P)
Hervé Lang (H)
Eric Voog (E)
Eric Mandron (E)
Jean Marc Tourani (JM)
Camille Serrate (C)
Alexandre Colau (A)
Carolina Saldana (C)
Alexandre DE LA Taille (A)
Thierry Nguyen (T)
François Kleinclauss (F)
Yohan Loriot (Y)
Jacques Irani (J)
Jean Christophe Eymard (JC)
Stéphane Larre (S)
Olivier Huillard (O)
Marc Zerbib (M)
Frédéric Rolland (F)
Jérôme Rigaud (J)
Nadine Houede (N)
Stéphane Droupy (S)
Georgina Malouf (G)
Morgan Roupret (M)
Sabine Vieillot (S)
Nicolas Letang (N)
Tiffen Lharidon (T)
Nicolas Gaschignard (N)
Werner Hilgers (W)
Jean Louis Davin (JL)

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests We declare no competing interests.

Auteurs

Christian Pfister (C)

Department of Urology, Charles Nicolle University Hospital, Rouen, France; Clinical Investigation Center, Onco-Urology, Inserm 1404, Rouen, France. Electronic address: christian.pfister@chu-rouen.fr.

Gwenaelle Gravis (G)

Department of Medical Oncology, Paoli-Calmette Institute, Marseille, France.

Aude Flechon (A)

Department of Medical Oncology, Léon Bérard Cancer Center, Lyon, France.

Christine Chevreau (C)

Department of Medical Oncology, ICR-IUCT Oncopole, Toulouse, France.

Hakim Mahammedi (H)

Department of Medical Oncology, Jean Perrin Cancer Center, Clermont-Ferrand, France.

Brigitte Laguerre (B)

Department of Medical Oncology, Eugène Marquis Cancer Center, Rennes, France.

Aline Guillot (A)

Department of Medical Oncology, Lucien Neuwirth Cancer Institute, St Priest, France.

Florence Joly (F)

Department of Medical Oncology, Baclesse Cancer Center, Caen, France.

Michel Soulie (M)

Department of Urology, Rangueil University Hospital, Toulouse, France.

Yves Allory (Y)

Department of Pathology, Curie Institute, Saint-Cloud, France.

Valentin Harter (V)

North-West Canceropole Data Center, Baclesse Cancer Center, Caen, France.

Stéphane Culine (S)

Department of Medical Oncology, Saint-Louis Hospital, AP-HP, Université de Paris, Paris, France.

Classifications MeSH