Circulating Basophils as a Prognostic Marker for Response to Bacillus Calmette-Guérin.

Bacillus Calmette-Guérin (BCG) therapy Bladder cancer Transurethral resection of bladder tumor (TURBT)

Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
15 Dec 2023
Historique:
received: 11 10 2023
revised: 01 12 2023
accepted: 10 12 2023
medline: 8 1 2024
pubmed: 8 1 2024
entrez: 7 1 2024
Statut: aheadofprint

Résumé

To predict recurrence and progression in non-muscle-invasive bladder cancer (NMIBC) patients receiving bacillus Calmette-Guérin (BCG), we evaluated circulating basophils as a biomarker that could be detected from the complete blood count. We use a pooled cohort of patients from the Centre Hospitalier Universitaire de Québec-Université Laval (2016-2020) and the Vancouver General Hospital (2010-2018) where a complete blood count was available before transurethral resection of bladder tumor (TURBT) of a high-grade NMIBC and subsequent BCG. Descriptive statistics described the cohort based on the dichotomous presence or absence of basophils on the complete blood count. Kaplan-Meier estimates and a log-rank test compared recurrence-free survival (RFS) and progression-free survival (PFS), with multivariable cox regression analysis used to estimate proportional hazard ratios. The study cohort included 261 patients, with a median follow-up of 31.5 months (interquartile range 18.1-45.0 months). The median age was 74.0 years and 16.8% were female. Circulating basophils were detectable in 49 (18.9%) patients. Both RFS and PFS were significantly lower in patients with detectable basophils. Multivariable analysis demonstrated detectable basophils were an independent predictor of both recurrence (HR = 1.85; 95% confidence interval [CI] 1.20-2.85; P = .01) and progression (HR = 2.29; 95% CI 1.14-4.60; P = .02). Our results confirm that baseline levels of circulating basophils are an immunological biomarker to predict recurrence and progression of NMIBC.

Identifiants

pubmed: 38185610
pii: S1558-7673(23)00271-9
doi: 10.1016/j.clgc.2023.12.004
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Geneviève Trépanier (G)

Department of Biology, Faculty of Medicine, Université Laval, Quebec City, Canada; Oncology Division, CHU de Québec-Université Laval Research Center, Quebec City, Canada.

Timo Nykopp (T)

Department of Surgery, University of Eastern Finland, Kuopio, Finland; Department of Urologic Sciences, Faculty of Medicine, University of British Columbia, Vancouver, Canada.

Raphaëlla Rosebush-Mercier (R)

Department of Surgery, Faculty of Medicine, Université Laval, Quebec City, Canada.

Typhaine Gris (T)

Oncology Division, CHU de Québec-Université Laval Research Center, Quebec City, Canada.

Jonathan Fadel (J)

Department of Surgery, Faculty of Medicine, Université Laval, Quebec City, Canada.

Peter C Black (PC)

Department of Urologic Sciences, Faculty of Medicine, University of British Columbia, Vancouver, Canada.

Paul Toren (P)

Oncology Division, CHU de Québec-Université Laval Research Center, Quebec City, Canada; Department of Surgery, Faculty of Medicine, Université Laval, Quebec City, Canada. Electronic address: paul.toren@crchudequebec.ulaval.ca.

Classifications MeSH