Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

Immunohistochemistry-Based Molecular Subtyping in Muscle-Invasive Bladder Cancer: Predicting Response to Neoadjuvant Chemotherapy.

Created on 13 Jul 2026

Authors

Luis Pérez-Bartivas, Fernando Leiva-Cepas, David Ponferrada, Pablo Flores-Paco, Víctor Atance-Morales, Marta Martínez, Ana Armenta-Triviño, Rosa María Rodríguez-Alonso, Juan De La Haba-Rodríguez, Enrique Aranda, María José Méndez-Vidal

Published in

Archivos espanoles de urologia. Volume 79. Issue 5. Pages 773-782.

Abstract

Muscle-invasive bladder cancer (MIBC) presents a heterogeneous response to perioperative chemotherapy. Although several molecular classifications of MIBC have been proposed, two main subtypes, namely, luminal and basal, are widely recognised. This study aims to explore the relationship between the molecular subtypes of MIBC, as characterised by GATA binding protein 3 (GATA3) and cytokeratin 5/6 (CK5/6) immunohistochemistry, and treatment response to neoadjuvant chemotherapy.
Patients with nonmetastatic MIBC who were treated with cisplatin-based neoadjuvant chemotherapy at the Reina Sofía University Hospital between 2014 and 2023 were retrospectively analysed. Tumours were classified into luminal (GATA3+, CK5/6-), basal (GATA3-, CK5/6+), double-positive (GATA3+, CK5/6+), or double-negative (GATA3-, CK5/6-) subtypes. Clinical and pathological data, including overall survival (OS), disease-free survival (DFS) and pathological response, were analysed by using Kaplan-Meier curves, log-rank tests and chi-squared tests.
Amongst the 69 patients included, 13 were classified as luminal, five as basal, 50 as double positive and one as double negative. Patients with luminal tumours had significantly higher five-year DFS (91.7% vs. 50.7%, p = 0.021) and OS (100% vs. 60.5%, p = 0.016) than those with double-positive tumours. Pathological complete response (ypT0) was observed in 7/13 (53.8%) luminal tumours and in 15/50 (30.0%) double-positive tumours (p = 0.190). Additionally, 9/13 (69.2%) luminal tumours achieved tumour downstaging (p = 0.060) achieved tumour downstaging. Basal and double-negative subtypes were excluded from analysis because of their low representation in the sample.
The luminal subtype showed superior outcomes in terms of DFS and OS compared with double-positive tumours. Higher rates of pathological complete response and tumour downstaging were observed in luminal tumours than in other tumour types. However, these differences did not reach statistical significance.

PMID:
42438872
Bibliographic data and abstract were imported from PubMed on 13 Jul 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 2
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement