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E-Poster Display

690TiP - A phase III, randomized, double-blind trial of nivolumab or placebo combined with docetaxel for metastatic castration-resistant prostate cancer (mCRPC; CheckMate 7DX)

Date

17 Sep 2020

Session

E-Poster Display

Topics

Immunotherapy

Tumour Site

Prostate Cancer

Presenters

Charles Drake

Citation

Annals of Oncology (2020) 31 (suppl_4): S507-S549. 10.1016/annonc/annonc275

Authors

C.G. Drake1, F. Saad2, W.R. Clark3, M. Ciprotti4, B. Sharkey5, S.K. Subudhi6, K. Fizazi7

Author affiliations

  • 1 Medical Oncology, Columbia University Irving Cancer Center, 10032 - New York/US
  • 2 Department Of Urology, Centre Hospitalier de l’Université de Montréal/CHUM, H2X 0A9 - Montreal/CA
  • 3 Urology, Alaska Clinical Research Center, 99503 - Anchorage/US
  • 4 Oncology Clinical Development, Bristol-Myers Squibb Company, UB8 1DH - Uxbridge/GB
  • 5 Biometrics And Data Sciences, Bristol-Myers Squibb Company, 08540 - Princeton/US
  • 6 Department Of Genitourinary Medical Oncology, MD Anderson Cancer Center, University of Texas, 77030 - Houston/US
  • 7 Department Of Cancer Medicine, Gustave Roussy, 94805 - Villejuif/FR

Resources

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Abstract 690TiP

Background

Treatment with docetaxel, a recommended first-line chemotherapy for mCRPC, may enhance antitumor immune responses by (1) increasing neoantigen presentation, (2) stimulating proinflammatory cytokine secretion, and (3) downregulating suppressive immune cell populations. Immunotherapy may augment these effects, providing a strong rationale for combining immune checkpoint blockade with docetaxel in patients with mCRPC. In support of this hypothesis, the phase 2 CheckMate 9KD trial showed that combining the anti–PD-1 antibody nivolumab with docetaxel had promising clinical activity in patients with mCRPC. In this randomized, double-blind phase III trial (CheckMate 7DX), we will evaluate the combination of nivolumab plus docetaxel versus placebo plus docetaxel for men with mCRPC (NCT04100018).

Trial design

Key inclusion criteria are histologically confirmed adenocarcinoma of the prostate with current evidence of metastatic disease, ECOG performance status 0–1, ongoing androgen deprivation therapy with a gonadotropin-releasing hormone analogue or bilateral orchiectomy, documented progression per PCWG3 criteria within 6 months before screening, no prior chemotherapy in the mCRPC setting, 1–2 prior second-generation hormonal therapies, and available tumor tissue for biomarker analysis. Key exclusion criteria are active brain metastases, conditions requiring systemic corticosteroid/immunosuppressive treatment, autoimmune disease, and prior treatment targeting T-cell co-stimulation or checkpoint pathways. Patients are randomized 1:1 to nivolumab + docetaxel (arm A) or placebo + docetaxel (arm B), followed by nivolumab (arm A) or placebo (arm B) alone. Docetaxel will be administered for a maximum of 10 cycles; nivolumab will be administered for a maximum of 2 years. Primary endpoints are radiographic progression-free survival per PCWG3 and overall survival. Secondary endpoints include objective response rate and duration of response per PCWG3, prostate-specific antigen response rate, safety, and pain progression (assessed by the Brief Pain Inventory-Short Form). Enrollment is ongoing with a target of 984 randomized patients.

Clinical trial identification

NCT04100018.

Editorial acknowledgement

Professional medical writing assistance was provided by Richard Daniel, PhD, of Parexel, funded by Bristol-Myers Squibb Company.

Legal entity responsible for the study

Bristol-Myers Squibb Company.

Funding

Bristol-Myers Squibb Company and ONO Pharmaceutical Company Limited.

Disclosure

C.G. Drake: Advisory/Consultancy, Research grant/Funding (self), Shareholder/Stockholder/Stock options: Compugen; Advisory/Consultancy: Roche/Genentech; Advisory/Consultancy, Research grant/Funding (self): Janssen Oncology; Advisory/Consultancy: Pfizer; Advisory/Consultancy: Astellas Medivation; Advisory/Consultancy, Shareholder/Stockholder/Stock options: Tizona Therapeutics; Advisory/Consultancy: Merck; Advisory/Consultancy: Pierre Fabre; Advisory/Consultancy: F-Star; Advisory/Consultancy, Shareholder/Stockholder/Stock options: KLEO; Advisory/Consultancy, Shareholder/Stockholder/Stock options: Harpoon; Advisory/Consultancy, Shareholder/Stockholder/Stock options: Shattuck Labs; Advisory/Consultancy, Shareholder/Stockholder/Stock options: Werewolf; Advisory/Consultancy: Genocea; Advisory/Consultancy, Patent: Amplimmune; Advisory/Consultancy, Patent: BMS; Advisory/Consultancy: EMD; Advisory/Consultancy: Sanofi Aventis. F. Saad: Honoraria (self), Advisory/Consultancy, Research grant/Funding (self), Research grant/Funding (institution): BMS. W.R. Clark: Research grant/Funding (self), Principal investigator for studies: BMS; Research grant/Funding (self), Principal investigator for studies: Astellas; Research grant/Funding (self), Principal investigator for studies: Pfizer; Research grant/Funding (self), Principal investigator for studies: Seattle Genetics; Research grant/Funding (self), Principal investigator for studies: Merck; Research grant/Funding (self), Principal investigator for studies: Bayer. M. Ciprotti: Shareholder/Stockholder/Stock options, Full/Part-time employment: Bristol Myers Squibb. B. Sharkey: Shareholder/Stockholder/Stock options, Full/Part-time employment: Bristol Myers Squibb. S.K. Subudhi: Advisory/Consultancy, Research grant/Funding (self): Janssen Oncology; Advisory/Consultancy: Polaris; Advisory/Consultancy: Dendreon; Advisory/Consultancy, Shareholder/Stockholder/Stock options, Ownership interests: Apricity Health; Advisory/Consultancy: Amgen; Advisory/Consultancy: Bayer; Advisory/Consultancy: Exelixis; Advisory/Consultancy, Research grant/Funding (self): AstraZeneca; Advisory/Consultancy, Research grant/Funding (self): Bristol-Myers Squibb ; Advisory/Consultancy: Dava Oncology; Advisory/Consultancy: Cancer Now; Advisory/Consultancy: MEDACorp; Advisory/Consultancy: Parker Institute of Cancer Immunotherapy; Advisory/Consultancy: Society for Immunotherapy of Cancer. All other authors have declared no conflicts of interest.

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