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Neoadjuvant vs. Adjuvant Chemotherapy in Muscle Invasive Bladder Cancer (MIBC): Analysis From the RISC Database

Authors :
Gabriella Del Bene
Fabio Calabrò
Diana Giannarelli
Elizabeth R. Plimack
Lauren C. Harshman
Evan Y. Yu
Simon J. Crabb
Sumanta Kumar Pal
Ajjai S. Alva
Thomas Powles
Ugo De Giorgi
Neeraj Agarwal
Aristotelis Bamias
Sylvain Ladoire
Andrea Necchi
Ulka N. Vaishampayan
Günter Niegisch
Joaquim Bellmunt
Jack Baniel
Matthew D. Galsky
Cora N. Sternberg
Source :
Frontiers in Oncology, Vol 8 (2018)
Publication Year :
2018
Publisher :
Frontiers Media S.A., 2018.

Abstract

Background: MIBC is an aggressive disease, with 5-year survival rates ranging from 36 to 48% for p T3/p T4/p N+tumors. Perioperative treatment can improve overall survival, with more robust evidence in favor of neoadjuvant chemotherapy. Few randomized studies have compared neoadjuvant and adjuvant therapy in bladder cancer. Consequently, it has been difficult to establish the benefit of adjuvant chemotherapy (AC) in MIBC.Methods: Data from patients with muscle invasive bladder cancer (>pT2) collected from 2005 to 2012 within the RISC data base (Retrospective International Study of Cancers of the Urothelial Tract) were evaluated. Overall survival (OS), cancer specific survival (CSS), and disease-free survival (DFS) between NC and AC generated using the Kaplan-Meier method were compared for MIBC by log-rank test. All patients in this analysis received either NC or AC.Results: A total of 656 patients with MIBC (325 treated with AC and 331 with NC) were analyzed. The median DFS was 34.6 months (95% CI:25.3–43.9) for NC vs. 24.9 months (95% CI: 19.4–30.5) with AC, with a reduction in the risk of disease progression of 21% in favor of NC (HR: 0.78, 95% CI: 0.63–0.96, P = 0.02). There were no significant differences in terms of CSS (HR: 1.06, 95% CI: 0.79–1.43, P: 0.70), and OS (HR: 1.08, 95% CI: 0.83–1.39, P = 0.57).Conclusions: This study demonstrates superiority in DFS for NC compared to AC. The positive prognostic impact of complete pathological response to NC was confirmed.

Details

Language :
English
ISSN :
2234943X
Volume :
8
Database :
Directory of Open Access Journals
Journal :
Frontiers in Oncology
Publication Type :
Academic Journal
Accession number :
edsdoj.07c29ee921bc45cdbbe4ef5cab278458
Document Type :
article
Full Text :
https://doi.org/10.3389/fonc.2018.00463