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Poster session 11

1656TiP - The STAMPEDE2 niraparib-abiraterone acetate + prednisolone trial: A phase III, randomised, open-label trial in patients with metastatic prostate cancer (mPC) with a deleterious alteration in a homologous recombination repair (HRR) gene starting androgen deprivation therapy (ADT)

Date

14 Sep 2024

Session

Poster session 11

Topics

Targeted Therapy

Tumour Site

Prostate Cancer

Presenters

Sarah Howlett

Citation

Annals of Oncology (2024) 35 (suppl_2): S962-S1003. 10.1016/annonc/annonc1607

Authors

S. Howlett1, M. Kayani2, L.C. Brown2, C.L. Amos2, P. Dutey-Magni2, Y. Yogeswaran2, L. O'Shea2, C. Hogan2, A. Wingate1, S. Lall1, R. Eeles3, M. Hubank4, P. Williams2, W. Cross5, A. Sachdeva6, N. Clarke7, M.K. Parmar2, N.D. James8, E. Grist1, G. Attard1

Author affiliations

  • 1 Research Department Of Oncology, UCL Cancer Institute - Paul O'Gorman Building, WC1 E6JD - London/GB
  • 2 Mrc Clinical Trials Unit, MRC - Medical Research Council Clinical Trials Unit - University College London (UCL), WC1V 6LJ - London/GB
  • 3 Oncogenetics, Royal Marsden Hospital Institute of Cancer Research, SM2 5NG - Sutton/GB
  • 4 Clinical Genomics, ICR - The Institute of Cancer Research - North Site, SM2 5NG - Sutton/GB
  • 5 Department Of Urology, University of Leeds - Leeds Institute of Molecular Medicine (LIMM), LS9 7TF - Leeds/GB
  • 6 Division Of Cancer Sciences, The University of Manchester, M13 9PL - Manchester/GB
  • 7 Department Of Urology, The Christie and Salford Royal NHS Foundation Trusts, Manchester/GB
  • 8 Prostate And Bladder Cancer Research Department, ICR - Institute of Cancer Research, SW7 3RP - London/GB

Resources

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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.

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