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E-Poster Display

883TiP - MOONSTONE/GOG-3032: A phase II, open-label, single-arm study to evaluate the efficacy and safety of niraparib + dostarlimab in patients with platinum-resistant ovarian cancer

Date

17 Sep 2020

Session

E-Poster Display

Topics

Immunotherapy

Tumour Site

Ovarian Cancer

Presenters

Leslie Randall

Citation

Annals of Oncology (2020) 31 (suppl_4): S551-S589. 10.1016/annonc/annonc276

Authors

L.M. Randall1, D.M. O'Malley2, B.J. Monk3, R.L. Coleman4, R.E. O'Cearbhaill5, S. Gaillard6, S. Adams7, F. Cappuccini8, M. Huang9, H.S. Chon10, A.A. Secord11, S. Arora12, E. Keeton12, D. Gupta12, V. Samnotra12, P. Konstantinopoulos13

Author affiliations

  • 1 Department Of Obstetrics And Gynecology, Massey Cancer Center, Virginia Commonwealth University, 23298-0037 - Richmond/US
  • 2 Department Of Obstetrics And Gynecology, The Ohio State University – James CCC, Columbus/US
  • 3 Gynecologic Oncology Department, University of Arizona College of Medicine, Phoenix/US
  • 4 Gynecologic Oncology Department, University of Texas MD Anderson Cancer Center, Houston/US
  • 5 Medical Oncology Department, Memorial Sloan Kettering Cancer Center, New York/US
  • 6 Gynecology And Obstetrics Department, Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore/US
  • 7 Department Of Obstetrics And Gynecology, The University of New Mexico Comprehensive Cancer Center, Albuquerque/US
  • 8 Division Of Gynecologic Oncology, Chao Family Comprehensive Cancer Center, University of California-Irvine Medical Center, Orange/US
  • 9 Department Of Obstetrics And Gynecology, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami/US
  • 10 Gynecologic Oncology Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa/US
  • 11 Obstetrics And Gynecology Department, Duke University Medical Center and Duke Cancer Institute, Durham/US
  • 12 Clinical Science, GlaxoSmithKline, Waltham/US
  • 13 Division Of Gynecologic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston/US

Resources

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Abstract 883TiP

Background

Niraparib, a poly(ADP-ribose) polymerase inhibitor (PARPi), is approved in the US and Europe for maintenance treatment of patients (pts) with recurrent ovarian (OC), fallopian tube, or primary peritoneal cancer following complete or partial response to platinum-based chemotherapy (chemo), and in the US for the treatment of pts with advanced OC who have been treated with ≥3 prior chemo regimens and whose cancer is BRCA mutated, regardless of platinum sensitivity, or associated with homologous recombination deficiency and platinum sensitivity. Pts with recurrent OC often develop platinum-resistant OC (PROC). In the US, approved treatments for PROC include bevacizumab + chemo. However, despite these therapies, improved outcomes for pts with PROC remain an unmet need. PARPi + anti–programmed death (PD)-1 combinations may have a synergistic antitumor effect. The objective of this currently enrolling study is to evaluate the safety and efficacy of niraparib + dostarlimab (an investigative anti–PD-1 humanized monoclonal antibody) in pts with advanced, relapsed, high-grade PROC without a known BRCA mutation that received and progressed on prior bevacizumab.

Trial design

Eligible pts must have recurrent high-grade serous, endometrioid, or clear cell ovarian, fallopian tube, or primary peritoneal cancer, received 1−3 lines of prior therapy (one of which included bevacizumab), and have disease progression <6 months from the last administered platinum-based chemo. Those having received a prior PARPi, anti–PD-1, or anti–programmed death-ligand 1 (PD-L1), or with a known or suspected deleterious BRCA mutation, are ineligible. Approximately 150 pts will be enrolled in the US and receive dostarlimab 500 mg IV Q3W for the first 4 doses and then 1000 mg IV Q6W for up to 3 years or until disease progression or toxicity. Pts with baseline bodyweight <77 kg or platelet count <150,000/μL will receive a 200-mg QD starting dose of niraparib, all other pts will receive a 300-mg QD starting dose. The primary endpoint is investigator-assessed objective response rate per RECIST v1.1 in the overall population and PD-L1+ subsets.

Clinical trial identification

NCT03955471.

Editorial acknowledgement

Writing and editorial support, funded by GlaxoSmithKline (Waltham, MA, USA) and coordinated by Hasan Jamal, MSc of GlaxoSmithKline, was provided by Eric Scocchera, PhD and Anne Cooper, MA of Ashfield Healthcare Communications (Middletown, CT, USA).

Legal entity responsible for the study

GlaxoSmithKline, Waltham, MA, USA.

Funding

GlaxoSmithKline, Waltham, MA, USA.

Disclosure

L.M. Randall: Advisory/Consultancy: GlaxoSmithKline; Advisory/Consultancy: Tesaro. D.M. O'Malley: Advisory/Consultancy: Tesaro, Immunogen, Eisai, Agenus, GSK; Advisory/Consultancy: Clovis; Advisory/Consultancy: Ambry, AbbVie; Advisory/Consultancy: Janssen/J&J, Renegeron, Novacure, Myriad Genetics, Tarveda; Advisory/Consultancy: Amgen; Advisory/Consultancy: Genentech/Roche, Merck; Research grant/Funding (institution): VentiRx, Array Biopharma, EMD Serono, Ergomed; Research grant/Funding (institution): Ajinomoto Inc, Ludwig Cancer Research; Research grant/Funding (institution): Stemcentrx Inc., Tracon Pharmaceuticals, GOG Foundation; Research grant/Funding (institution): Yale University, New Mexico Cancer Care Alliance; Research grant/Funding (institution): INC Research Inc., Inventiv Health Clinical; Research grant/Funding (institution): Iovance Biotherapeutics, Inc, PRA Intl. B.J. Monk: Advisory/Consultancy, Research grant/Funding (institution): Tesaro. R.L. Coleman: Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): Merck; Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): Roche; Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): Genentech; Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): AstraZeneca; Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): Janssen; Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): Clovis; Research grant/Funding (institution): V-Foundation; Research grant/Funding (institution): Genmab; Honoraria (institution), Advisory/Consultancy: Oncomed/Mateo; Honoraria (institution), Advisory/Consultancy: Novocure; Honoraria (institution), Advisory/Consultancy: Onosec; Honoraria (institution), Advisory/Consultancy: Tesaro/GSK; Honoraria (institution), Advisory/Consultancy: Eisai; Honoraria (institution), Advisory/Consultancy: Arrivive; Honoraria (institution), Advisory/Consultancy: OncoQuest; Advisory/Consultancy, Research grant/Funding (institution): AbbVie. R.E. O'Cearbhaill: Advisory/Consultancy: Tesaro, AstraZeneca; Advisory/Consultancy: GlaxoSmithKline; Research grant/Funding (institution): NIH/NCI. S. Gaillard: Advisory/Consultancy: Immunogen; Advisory/Consultancy, Research grant/Funding (institution): AstraZeneca; Advisory/Consultancy, Licensing/Royalties: Semonix Pharmaceuticals; Advisory/Consultancy: Rigel; Research grant/Funding (institution): PharmaMar; Research grant/Funding (institution): Genentech; Research grant/Funding (institution): Roche; Research grant/Funding (institution): Iovance Biotherapeutics; Research grant/Funding (institution): AbbVie; Research grant/Funding (institution): Pfizer; Research grant/Funding (institution): Tesaro. S. Adams: Research grant/Funding (institution): AstraZeneca. M. Huang: Advisory/Consultancy: Tesaro; Advisory/Consultancy: Clovis; Advisory/Consultancy: Janssen; Research grant/Funding (institution): Merck; Research grant/Funding (institution): Lily. A.A. Secord: Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): Tesaro; Research grant/Funding (institution): AbbVie; Research grant/Funding (institution): Amgen; Research grant/Funding (institution): Astex Pharmaceuticals Inc.; Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): AstraZeneca; Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): Clovis; Research grant/Funding (institution): Astellas Pharma Inc.; Research grant/Funding (institution): Boehringer Ingelheim; Research grant/Funding (institution): Bristol-Myers Squibb; Research grant/Funding (institution): Eisai; Research grant/Funding (institution): Endocyte; Research grant/Funding (institution): Exelixis; Research grant/Funding (institution): Incyte; Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): Merck; Research grant/Funding (institution): PharmaMar; Research grant/Funding (institution): Immutep Ltd.; Honoraria (institution), Advisory/Consultancy, Research grant/Funding (institution): Roche/Genentech; Research grant/Funding (institution): Seattle Genetics, Inc.; Research grant/Funding (institution): TapImmune; Honoraria (institution), Advisory/Consultancy: Alexion; Honoraria (institution), Advisory/Consultancy: Aravive; Honoraria (institution), Advisory/Consultancy: Janssen/Johnson & Johnson; Honoraria (institution), Advisory/Consultancy: Mersana; Honoraria (institution), Advisory/Consultancy: Myriad; Honoraria (institution), Advisory/Consultancy: Oncoquest. S. Arora, E. Keeton, D. Gupta, V. Samnotra: Full/Part-time employment: GlaxoSmithKline. P. Konstantinopoulos: Advisory/Consultancy: Merck; Advisory/Consultancy: Pfizer; Advisory/Consultancy: AstraZeneca. All other authors have declared no conflicts of interest.

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