Abstract 1656TiP
Background
Treatment intensification at the start of ADT improves overall survival (OS) in mPC. Up to 15% of mPC harbour a deleterious alteration in BRCA2 or a related HRR gene that confers sensitivity to polyadenosine diphosphate-ribose polymerase inhibitors. STAMPEDE2 will test for benefit from Niraparib-Abiraterone Acetate + Prednisolone in HRR-altered mPC starting ADT.
Trial design
STAMPEDE2 is a phase III, randomised, open label, multi-centre platform protocol testing treatments in metastatic hormone sensitive prostate cancer (NCT06320067, ISRCTN66357938). For the Niraparib-Abiraterone Acetate + Prednisolone trial, patients identified as biomarker positive (HRR gene alteration) on clinical next-generation tumour sequencing are offered randomisation 1:1 to either arm A (standard of care with physician’s choice androgen receptor signalling inhibitor [SoC ARSI]) or arm N (standard of care with Niraparib-Abiraterone Acetate + Prednisolone) (Table). Prior randomisation into the STAMPEDE2 SABR or PSMA-Lutetium trials is allowed. Randomisation is stratified by planned use of Docetaxel and/or prostate radiotherapy (RT) and/or SABR/PSMA-Lutetium. Target recruitment is 680 patients with the primary outcomes Overall Survival (OS). Target HR=0.65, 80% power. The Niraparib-Abiraterone Acetate + Prednisolone trial is a collaboration with Janssen Pharmaceutica NV, sponsored by University College London (UCL), and co-ordinated by the MRC CTU at UCL. Table: 1656TiP
Key exclusion criteria | >6 months ADT |
Evidence of PSA progression on ADT +/- ARSI | |
Interventions | Arm A: SoC ARSI |
Arm N: ADT + 2 regular-strength dual-action tablets 100 mg Niraparib/500mg Abiraterone Acetate per tablet (total dose 200 mg Niraparib/1000 mg Abiraterone Acetate) + Prednisolone 5mg OD | |
Arms A&N: +/- Docetaxel +/- Prostate RT +/- SABR +/- PSMA-Lutetium Treat until radiographic progression, unacceptable toxicity or death | |
Primary endpoints | OS |
Secondary endpoints | Radiographic progression free survival |
Failure free survival | |
Prostate cancer specific survival | |
Toxicity | |
Quality of life | |
Cost-effectiveness |
Clinical trial identification
NCT06320067, ISRCTN66357938.
Editorial acknowledgement
Legal entity responsible for the study
University College London.
Funding
Janssen.
Disclosure
L.C. Brown: Financial Interests, Institutional, Research Grant, £170k educational grant for the FOCUS4-C Trial from June 2017 to Dec 2021: AstraZeneca; Financial Interests, Institutional, Funding, Various grants awarded to my institution for work undertaken as part of the STAMPEDE Trial: janssen pharmaceuticals; Financial Interests, Institutional, Funding, Grant funding to my institution for the STAMPEDE2 trial.: Novartis AAA; Non-Financial Interests, Other, I am a member of the CRUK CERP funding advisory panel and my Institution also receive grant funding from CRUK for the STAMPEDE and FOCUS4 trials: Cancer Research UK. W. Cross: Financial Interests, Personal, Speaker, Consultant, Advisor: AAA Novartis, Bayer, Janssen, Astellas, Ipsen, Myriad Genetics, Allied Healthcare. M.K. Parmar: Financial Interests, Institutional, Full or part-time Employment, Director at MRC Clinical Trials Unit at UCL: Medical Research Council Clinical Trials Unit at UCL; Financial Interests, Personal and Institutional, Research Grant: AstraZeneca, Astellas, Janssen, Baxter, GSK; Financial Interests, Institutional, Research Grant: Clovis, Abcodia Pvt Ltd., Akagera, Amgen, Aspirin Foundation, Bayer, BMS US, Bri-BioCepheid, Cipla, CSL Behring, Eli Lilly, Emergent Biosolutions, Gilead Sciences, Grifols, Johnson & Johnson, Pfizer, Sanofi, ViiVHealthcare, Micronoma, Modus Theraputics, Mylan, Serum Institute of India, shionogi, SyntenyBiotechnology, Takeda, Tibotec, Transgene, Virco and Xenothera; Non-Financial Interests, Advisory Role, Euro Ewing Consortium: University College London; Non-Financial Interests, Advisory Role, rEECur: University of Birmingham; Non-Financial Interests, Advisory Role, CompARE Trial: University of Birmingham; Non-Financial Interests, Advisory Role, ROSSINI Trial Platform: University of Birmingham. N.D. James: Financial Interests, Personal, Advisory Board, Advice around PARP inhibitors: AstraZeneca; Financial Interests, Personal, Advisory Board, Prostate cancer therapies: Janssen, Clovis, Novartis; Financial Interests, Institutional, Advisory Board, Assisted with submissions regarding licencing for abiraterone: Janssen; Financial Interests, Personal, Advisory Board, Docetaxel: Sanofi; Financial Interests, Institutional, Advisory Board, Providing STAMPEDE trial data to facilitate licence extensions internationally for docetaxel: Sanofi; Financial Interests, Personal, Advisory Board, Bladder cancer therapy: Merck; Financial Interests, Personal, Advisory Board, Advice around novel hormone therapies for prostate cancer: Bayer; Financial Interests, Personal, Invited Speaker, Lecture tour in Brazil August 2022 - speaking on therapy for advanced prostate cancer: Merck Sharp & Dohme (UK) Limited; Financial Interests, Institutional, Coordinating PI, Funding for STAMPEDE trial: Janssen, Astellas; Financial Interests, Institutional, Coordinating PI, Funding for RADIO trial bladder cancer: AstraZeneca. G. Attard: Financial Interests, Personal, Invited Speaker: Janssen, Astellas, AstraZeneca; Financial Interests, Personal, Advisory Board: Janssen, Astellas, Novartis, Bayer, AstraZeneca, Pfizer, Sanofi, Sapience, Orion, Novartis, Blue Earth Therapeutics; Financial Interests, Personal, Royalties, Included in list of rewards to discoverers of abiraterone: Institute of Cancer Research; Financial Interests, Institutional, Advisory Board: Artera, Veracyte; Financial Interests, Institutional, Research Grant: Janssen, Astellas, Novartis; Financial Interests, Institutional, Coordinating PI: Janssen; Financial Interests, Institutional, Local PI: Novartis, Pfizer; Non-Financial Interests, Principal Investigator: Janssen, Astellas; Non-Financial Interests, Advisory Role: Janssen, AstraZeneca; Non-Financial Interests, Project Lead: Artera, Veracyte. All other authors have declared no conflicts of interest.
Resources from the same session
1687P - Perceptions of genetic testing and lived experiences in women with locally advanced or metastatic ovarian cancer: A focus on BRCAm and BRCAwt patients
Presenter: María Jesús Rubio Pérez
Session: Poster session 11
1688P - Psychosocial distress and spirituality among elderly patients with cancer in Nigeria
Presenter: Zainab Ogunjimi
Session: Poster session 11
1689TiP - The social stigma of smokers and patients with lung cancer: Detection of phoenomenon and testing of EMDR (eye movement desensitization and reprocessing) intervention
Presenter: Domenico Galetta
Session: Poster session 11
1692P - A phase Ib/IIa trial to evaluate the safety and efficacy of PM8002/ BNT327, a bispecific antibody targeting PD-L1 and VEGF-A, as a monotherapy in patients with advanced renal cell carcinoma
Presenter: Xinan Sheng
Session: Poster session 11
1693P - CaboPoint: Final results from a phase II study of cabozantinib after checkpoint inhibitor (CPI) combinations in patients with advanced renal cell carcinoma (aRCC)
Presenter: Laurence Albiges
Session: Poster session 11
1695P - Phase I LITESPARK-018: Dose escalation study of belzutifan in advanced pretreated clear cell renal cell carcinoma (ccRCC)
Presenter: Ulka Vaishampayan
Session: Poster session 11
1696P - A phase I/ II trial of pazopanib (Paz) alternating (alt) with bevacizumab (Bev) in treatment-naïve metastatic clear cell renal cell carcinoma (mccRCC) patients (pts): Phase II results
Presenter: Saby George
Session: Poster session 11
1697P - Phase II randomized double-blind trial of axitinib (Axi) +/- PF 04518600, an OX40 antibody (PFOX) after PD1/PDL1 antibody (IO) therapy (Tx) in metastatic renal cell carcinoma (mRCC): Final analysis
Presenter: Sarmad Sadeghi
Session: Poster session 11
1698P - Avelumab + axitinib (Ave + Axi) vs sunitinib (Sun) in advanced renal cell carcinoma (aRCC): Final analysis of patient (pt)-reported outcomes (PROs) and quality-adjusted time without symptoms or toxicity (Q-TWiST)
Presenter: Balaji Venugopal
Session: Poster session 11