Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Cambridge Neoadjuvant Cancer of the Prostate (CANCAP03): A window study into the effects of Olaparib ± Degarelix in primary prostate cancer

Dev, Harveer, Linch, Mark, Narahari, Krishna ORCID: https://orcid.org/0000-0003-0257-7033, Milne-Clark, Toby, Cheung, Melissa, Warren, Anne, Malaviya, Alopa, Gnanapragasam, Vincent, Hernandez, Tatiana, Bullock, Nicholas, Machin, Andrea, Dayimu, Alimu, Robb, Tamsin, Cromwell, Elizabeth, Freeman, Alex, Harrington, Elizabeth A., Camacho, Niedzika, Glont, Silvia, Squatrito, Massimo, Rotem, Asaf, Moore, Luiza, Hanson, Robert, Dodd, Marc, Anand, Shubha, Kynaston, Howard ORCID: https://orcid.org/0000-0003-1902-9930, Shaw, Greg, Shah, Nimish and Pacey, Simon 2025. Cambridge Neoadjuvant Cancer of the Prostate (CANCAP03): A window study into the effects of Olaparib ± Degarelix in primary prostate cancer. Clinical Cancer Research 10.1158/1078-0432.ccr-24-1304

Full text not available from this repository.

Abstract

Purpose: The purpose was to investigate combined PARP and androgen inhibition in primary prostate cancer and understand the biological mechanisms underlying clinical efficacy, especially in the absence of mutations in homologous recombination (HR) repair pathways. Patients and Methods: The primary objective was to measure PARP inhibition, and the secondary objectives were to assess safety and feasibility. Participants received olaparib for 2 weeks before prostatectomy and were randomly assigned or not assigned (1:1) to degarelix. We analyzed diagnostic biopsy and radical prostatectomy samples for PARylated protein expression using IHC. Exploratory analyses included tumor gene sequencing, mutation analysis, and RNA sequencing (RNA-seq) using both bulk and single-cell RNA-seq performed on pretreatment and posttreatment tissues. Results: PARylated protein expression was significantly reduced in both cohorts, with no drug-related delays in radical prostatectomy. The gene set enrichment analysis identified distinct treatment response signatures related to olaparib in both cohorts and showed downregulation of androgen response genes after olaparib + degarelix treatment. Transcript profiling revealed an upregulation of the p53 hallmark, which was more pronounced with the combination treatment. Canonical cell-cycle progression hallmarks, including E2F targets and the G2–M checkpoint, were suppressed across all cases, correlating with a HR-deficient transcriptional signature. Single-nuclear RNA-seq indicated a greater increase in inflammatory response pathway activity within tumor epithelia after combination treatment. Conclusions: Transcriptomic analysis identified common hallmark alterations reflecting the combined impact of PARP inhibitor and androgen blockade on cell-cycle progression. We observed a shared phenotypic response to combination therapy across prostate cancers without known HR repair gene alterations. This suggests alternative mechanisms rather than antiandrogen-induced HR deficiency.

Item Type: Article
Date Type: Published Online
Status: In Press
Schools: Schools > Medicine
Publisher: American Association for Cancer Research
ISSN: 1078-0432
Date of Acceptance: 11 April 2025
Last Modified: 09 Jun 2025 10:00
URI: https://orca.cardiff.ac.uk/id/eprint/178897

Actions (repository staff only)

Edit Item Edit Item