Vesical Imaging‐Reporting and Data System use predicting the outcome of neoadjuvant pembrolizumab in muscle‐invasive bladder cancer

Author:

Necchi Andrea12,Basile Giuseppe3,Gibb Ewan A.4,Raggi Daniele1,Calareso Giuseppina5,de Padua Tiago Costa1,Patanè Damiano1,Crupi Emanuele1ORCID,Mercinelli Chiara1,Cigliola Antonio1,Tateo Valentina1,Giannatempo Patrizia6,Moschini Marco3,Briganti Alberto23,Montorsi Francesco23ORCID,Messina Antonella5,Ross Jeffrey S.78,Pavlick Dean7,De Cobelli Francesco29,Brembilla Giorgio9

Affiliation:

1. Department of Medical Oncology IRCCS Ospedale San Raffaele Milan Italy

2. Vita‐Salute San Raffaele University Milan Italy

3. Department of Urology IRCCS Ospedale San Raffaele Milan Italy

4. Veracyte, Inc San Francisco CA USA

5. Department of Radiology Fondazione IRCCS Istituto Nazionale dei Tumori Milan Italy

6. Department of Medical Oncology Fondazione IRCCS Istituto Nazionale dei Tumori Milan Italy

7. Foundation Medicine Inc Cambridge MA USA

8. SUNY Upstate Medical University Syracuse NY USA

9. Department of Radiology IRCCS Ospedale San Raffaele Milan Italy

Abstract

ObjectiveTo evaluate the predictive capability of the pre‐ and post‐pembrolizumab Vesical Imaging–Reporting and Data System (VI‐RADS) to identify ypT0N0 or ypT≤1N0 response in muscle‐invasive bladder cancer (MIBC) within the PURE‐01 trial (ClinicalTrials.gov identifier: NCT02736266).Patients and MethodsPatients were staged with bladder multiparametric magnetic resonance imaging (mpMRI) before and after treatment (three cycles of pembrolizumab) prior to radical cystectomy (RC). Logistic regression models were used to analyse the pre‐ and post‐ pembrolizumab VI‐RADS against ypT≤1N0 and ypT0N0 response. The VI‐RADS scores were dichotomised between 0 and 3 (0 = no evidence of disease) and 4–5. Event‐free survival (EFS) and overall survival (OS) analyses were performed. Comprehensive genomic profiling and transcriptome‐wide expression profiling data were matched with the VI‐RADS scores.ResultsIn total, 110 patients underwent centrally reviewed scans (N = 220 mpMRI), treated between February 2017 and July 2020. Both pre‐ and post‐pembrolizumab VI‐RADS 0–3 scores were the only significant covariates that predicted the ypT≤1N0 endpoint in multivariable analyses, and the strongest effect was seen with post‐pembrolizumab VI‐RADS 0–3 predicting the ypT≤1N0 response (P < 0.001). The area under the curve for this model was 0.90. Post‐pembrolizumab VI‐RADS 0–3 also predicted a longer EFS (P < 0.001) and OS (P = 0.044). The scores of several gene signatures from baseline tumours differed between the pre‐pembrolizumab VI‐RADS 0–3 and 4–5 categories.ConclusionPost‐pembrolizumab VI‐RADS scores are strongly associated with pathological downstaging and survival. VI‐RADS scores were also characterised by distinct biomarker features. These results indicate that the VI‐RADS is emerging as an important tool for designing next‐generation trials for MIBC.

Funder

Associazione Italiana per la Ricerca sul Cancro

Merck Sharp and Dohme

Publisher

Wiley

Subject

Urology

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