Abstract 175TiP
Background
Homologous recombination repair (HRR) genes are a common type of mutation in advanced prostate cancer, approximately 10-15% of metastatic hormonal sensitive prostate cancer (mHSPC) patients harbor loss-of-function mutations in the HRR genes. Olaparib plus Abiraterone and Prednisone combination therapy has significantly prolonged radiographic progress free survival in metastatic castration-resistant prostate cancer patients with or without HRR mutation. The efficacy of combination therapy at mHSPC stage deserves further exploration.
Trial design
Olaparib plus Abiraterone and Prednisone are being evaluated in a single-center, single-arm, prospective phase II study in newly diagnosed mHSPC patients with HRR gene mutation, and a total of 30 subjects will be enrolled in Drum Tower Hospital, Nanjing, China. Eligible subjects will receive a regimen of oral Olaparib tablets 300 mg twice daily plus Abiraterone 1000mg and Prednisone 5mg once daily, until radiographic disease progression (as assessed by the investigator per RECIST 1.1 and PCWG 3) or intolerable adverse reactions (as judged by the local investigator per the actual clinical situation). The primary endpoint of the study is radiographic progression-free survival (rPFS). The secondary end points are prostate-specific antigen (PSA) response, PSA-PFS, objective response rate and safety. Key eligibility criteria include: (1) Have a qualifying HRR genetic mutation in tumor tissue as determined by the central laboratory for this study. Satisfactory HRR gene mutations are BRCA1, BRCA2, ATM, BARD1, BRIP1, CDK12, CHEK1, CHEK2, FANCL, PALB2, RAD51B, RAD51C, RAD51D and RAD54L mutations. (2) Both archival or new biopsies are acceptable. (3) Prior treatment with any new hormone agent or any taxane will be excluded. 1 of planned 30 patients have been enrolled until May. 2022.
Clinical trial identification
NCT05167175.
Legal entity responsible for the study
The authors.
Funding
AstraZeneca China.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
150P - Use of neoadjuvant chemotherapy for non-metastatic muscle-invasive bladder cancer in Asia-Pacific
Presenter: Ravindran Kanesvaran
Session: Poster viewing 03
Resources:
Abstract
Slides
151P - Neoadjuvant and adjuvant chemotherapy in muscle-invasive bladder cancer: Real-world analysis of chemotherapy use and impact on patient outcomes
Presenter: Alison Hiong
Session: Poster viewing 03
152P - An epidemiologic study on PD-L1 expression with clinical observation of initial treatment pattern in the Chinese muscle invasive urothelial bladder carcinoma patients
Presenter: Liqun Zhou
Session: Poster viewing 03
153P - Efficacy and toxicity of HER2-targeted antibody-drug conjugates (ADCs) in the treatment of metastatic urothelial cancer (mUC): A systematic review
Presenter: Tiago Padua
Session: Poster viewing 03
154P - Can urine cytology predict variants of bladder cancer?
Presenter: Hikaru Mikami
Session: Poster viewing 03
155P - Search for circulating tumor cells in patients with urothelial cancer
Presenter: Irina Kruglova
Session: Poster viewing 03
156P - The association between response to enfortumab vedotin therapy and primary tumor location in Japanese urothelial carcinoma patients
Presenter: Nozomi Hayakawa
Session: Poster viewing 03
163P - Outcomes and toxicity of fosfesterol in metastatic castration-resistant prostate cancer: Experience from a low middle income country
Presenter: Manuprasad Avaronnan
Session: Poster viewing 03
164P - F-18 PSMA-PET/CT-guided percutaneous prostate biopsy
Presenter: Rajender Kumar
Session: Poster viewing 03
165P - Real-world utilisation of upfront chemohormonal therapy in metastatic hormone-sensitive prostate cancer
Presenter: Richard Kelly
Session: Poster viewing 03