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Mini Oral session 1

37MO - Dostarlimab plus chemotherapy in primary advanced or recurrent endometrial cancer (pA/rEC) in the RUBY trial: Overall survival (OS) by MMR status and molecular subgroups

Date

21 Jun 2024

Session

Mini Oral session 1

Topics

Tumour Site

Endometrial Cancer

Presenters

Robert Coleman

Citation

Annals of Oncology (2024) 9 (suppl_5): 1-8. 10.1016/esmoop/esmoop103499

Authors

M.A. Powell1, A. Auranen2, L.J. Willmott3, L. Gilbert4, D. Black5, D. Cibula6, S. Sharma7, G. Valabrega8, L.M. Landrum9, L.C. Hanker10, A. Stuckey11, I.A. Boere12, M. Gold13, M.S. Shahin14, B. Pothuri15, B.M. Slomovitz16, M. Grimshaw17, S. Stevens18, R.L. Coleman19, M.R. Mirza20

Author affiliations

  • 1 National Cancer Institute Sponsored NRG Oncology, Philadelphia/US
  • 2 Tampere University and Tampere University Hospital, Tampere/FI
  • 3 Arizona Cancer Care, Phoenix/US
  • 4 McGill University Health Centre, Montreal/CA
  • 5 LSU Health Shreveport, and Willis-Knighton Physician Network, Shreveport/US
  • 6 General University Hospital in Prague, First Faculty of Medicine, Charles University, Prague/CZ
  • 7 AMITA Adventist Hinsdale Hospital, Hinsdale/US
  • 8 Department of Oncology, University of Turin, Ordine Mauriziano Hospital, Torino/IT
  • 9 Simon Cancer Center, Indianapolis/US
  • 10 University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck/DE
  • 11 Women and Infants Hospital, Providence/US
  • 12 Erasmus MC Cancer Center, Rotterdam/NL
  • 13 Oklahoma Cancer Specialists and Research Institute, Tulsa/US
  • 14 Abington Hospital–Jefferson Health, Asplundh Cancer Pavilion, Sidney Kimmel Medical College of Thomas Jefferson University, Willow Grove/US
  • 15 NYU Langone Health, New York/US
  • 16 Mount Sinai Medical Center, and Department of Obstetrics and Gynecology, Florida International University, Miami Beach/US
  • 17 GSK, London/GB
  • 18 GSK, UB6 0HE - London/GB
  • 19 The US Oncology Network, The Woodlands/US
  • 20 Rigshospitalet, Copenhagen University Hospital, Copenhagen, and Nordic Society of Gynaecologic Oncology–Clinical Trial Unit, Copenhagen/DK

Resources

This content is available to ESMO members and event participants.

Abstract 37MO

Background

At interim analysis (IA) 1 of Part 1 of the RUBY trial (NCT03981796), statistically significant benefit in PFS was observed with dostarlimab+carboplatin-paclitaxel (D+CP) vs placebo (PBO)+CP in the overall and mismatch repair deficient/microsatellite instability-high (dMMR/MSI-H) populations of pts with pA/rEC. Here we report OS from IA2.

Methods

Pts with pA/rEC were randomized 1:1 to D+CP or PBO+CP followed by D or PBO for ≤3 years or until progression. OS was a dual-primary endpoint in the overall population and a prespecified, exploratory analysis in the dMMR/MSI-H and mismatch repair proficient/microsatellite stable (MMRp/MSS) populations. OS by molecular subgroup was a post-hoc analysis. Safety was a secondary endpoint.

Results

494 pts were randomized (245 D+CP; 249 PBO+CP). In the overall population, there was a significant reduction in the risk of death by 31% and clinically meaningful improvement of 16.4 mo in median OS (mOS) for D+CP vs PBO+CP (Table). In the dMMR/MSI-H population, hazard ratio (HR) for OS was 0.32; mOS was not reached for D+CP and was 31.4 mo for PBO+CP. In the MMRp/MSS population, HR for OS was 0.79; mOS was 34.0 mo for D+CP and 27.0 mo for PBO+CP. At IA2, in 400 pts with whole exome sequencing, a trend towards clinical benefit with D+CP was observed in the dMMR/MSI-H, TP53 mutated, and no specific molecular profile subgroups.

Table: 37MO

Safety at IA2 was similar to IA1

Dostarlimab+CP Placebo+CP OS, HR (95% CI)
Overall, N 245 249 0.69 (0.54–0.89)P=0.002
OS, median (95% CI), mo 44.6 (32.6–NR) 28.2 (22.1–35.6)
dMMR/MSI-H, n 53 65 0.32 (0.17–0.63)
OS, median (95% CI), mo NR (NR–NR) 31.4 (20.3–NR)
MMRp/MSS, n 192 184 0.79 (0.60–1.04)
OS, median (95% CI), mo 34.0 (28.6–NR) 27.0 (21.5–35.6)
Post hoc exploratory molecular subgroup analysis of OSa
POLEmut, n 2 3 No events in either arm
dMMR/MSI-H, n 39 52 0.40 (0.19–0.83)
TP53mut, n 47 41 0.59 (0.33–1.03)
NSMP, n 103 113 0.89 (0.61–1.29)

aAnalyses were conducted in 400 patients with whole exome sequencing results. Mut, mutant; NR, not reached; NSMP, no specific molecular profile.

Conclusions

D+CP showed statistically significant and clinically relevant OS benefit in the overall population compared with CP alone. A substantial survival difference was seen in the dMMR/MSI-H population. In the MMRp/MSS population, there was a 7 mo difference in median OS vs CP alone, with a 21% risk reduction for death. OS by molecular subgroup at IA2 was consistent with IA1. RUBY is the only trial to demonstrate a statistically significant OS benefit in pts with pA/rEC and supports the use of dostarlimab+CP as a standard of care in the 1L setting.

Clinical trial identification

NCT03981796.

Editorial acknowledgment

Writing and editorial support, funded and coordinated by GSK (Waltham, MA, USA), was provided by Shannon Morgan-Pelosi, PhD, CMPP, and Kathleen Blake, PhD, of Ashfield MedComms, an Inizio company. Portions of this data were previously presented at the Society of Gynecologic Oncology (SGO) 2024 Congress; March 16–18, 2024; San Diego, California and are presented on behalf of the original authors with their permission. Reused with permission.

Legal entity responsible for the study

GSK.

Funding

GSK.

Disclosure

M.A. Powell: Financial Interests, Personal, Research Grant: GSK; Financial Interests, Personal, Other, honoraria/consultation fees: AstraZeneca, Clovis Oncology, Eisai, GSK, Immunogen, Merck. A. Auranen: Financial Interests, Personal, Advisory Board: GSK, MSD. L.J. Willmott: Financial Interests, Personal, Speaker’s Bureau: AstraZeneca, Eisai, Immunogen, Merck, Seagen; Financial Interests, Personal, Advisory Board: AstraZeneca, Immunogen, Seagen. L. Gilbert: Financial Interests, Institutional, Other, Grants: Alkermes, AstraZeneca, Clovis, Esperas, ImmunoGen Inc, IMV, Karyopharm, Merck Sharp & Dohme, Mersana, Novocure GmbH, OncoQuest Pharmaceuticals, Pfizer, Roche, Tesaro; Financial Interests, Personal, Other, consulting fees: Merck; Financial Interests, Personal, Other, honoraria: Alkermes, AstraZeneca, Eisai, Eisai-Merck, GSK. D. Black: Financial Interests, Institutional, Other, grants: GSK; Financial Interests, Personal, Other, member: GOG Partners Investigational Council; Financial Interests, Personal, Other, medical director/owner: Trials365, LLC. D. Cibula: Financial Interests, Personal, Advisory Board: Akesobio, AstraZeneca, GSK, MSD, Novocure, Roche, Seagen, Sotio. G. Valabrega: Financial Interests, Personal, Other, consulting/advisory fees: Amgen, AstraZeneca, Clovis Oncology, GSK, PharmaMar, Roche, Tesaro. L.C. Hanker: Financial Interests, Personal, Other, consulting/advisory fees: Amgen, AstraZeneca, Clovis, Eisai, GSK, Intuitive Surgery, Janssen, MSD, Novartis, Pfizer, Pharma Mar, Roche, Tesaro. A. Stuckey: Financial Interests, Personal, Other, royalties: UptoDate reviewer. I.A. Boere: Financial Interests, Institutional, Research Grant: GSK; Financial Interests, Institutional, Advisory Board: AstraZeneca, GSK. M.S. Shahin: Financial Interests, Institutional, Other, grants: AstraZeneca, GSK, Merck; Financial Interests, Personal, Other, honoraria: AstraZeneca, GSK, Merck, Seagen; Financial Interests, Personal, Expert Testimony: Robindon & Havens PSC, Lexington KY; Financial Interests, Personal, Advisory Board: Seagen; Financial Interests, Personal, Other, board member: Unite for Her. B. Pothuri: Financial Interests, Institutional, Other, grant support: AstraZeneca, Celsion, Clovis Oncology, Eisai, Genentech/Roche, Karyopharm, Merck, Mersana, SeaGen, Sutro Biopharma, Takeda Pharmaceuticals, Tesaro/GSK, Toray, VBL Therapeutics; Financial Interests, Personal, Other, consulting fees: AstraZeneca, Atossa, Clovis Oncology, Deciphera, Elevar Therapeutics, Imab, Merck, Mersana, Sutro Biopharma, Tesaro/GSK, Toray; Other, Personal, Other, support for attending meetings: GOG Foundation; Financial Interests, Personal, Advisory Board: Arquer Diagnostics, AstraZeneca, Atossa, Clovis Oncology, Deciphera, Eisai, Elevar Therapeutics, GOGFoundation, Imab, Eli Lilly, Merck, Mersana, Seagen, Sutro Biopharma, Tesaro/GSK, Toray, VBL Therapeutics; Non-Financial Interests, Personal, Invited Speaker, leadership: NYOB Society Secretary, SGO Clinical Practice Committee Chair, SGO COVID-19 Taskforce Co-Chair. B.M. Slomovitz: Financial Interests, Personal, Advisory Board: AstraZeneca, Clovis, Genentech, GSK, GOG Foundation, Merck, Myriad, Jazz Pharma, Onconova, Nuvation Bio, EQRX, Regeneron, Eisai, Incyte; Financial Interests, Personal, Member of Board of Directors: GOG Foundation, HOW: Hearing Ovarian Cancer Whispers. M. Grimshaw, S. Stevens: Financial Interests, Personal, Full or part-time Employment: GSK. R.L. Coleman: Financial Interests, Personal, Other, grants or contracts: AstraZeneca, Clovis, Genelux, Genmab, Merck, Immunogen, Roche/Genentech; Financial Interests, Personal, Other, consulting fees: AbbVie, Agenus, Alkermes, AstraZeneca, Clovis, Deciphera, Genelux, Genmab, GSK, Immunogen, Novocure, Merck, OncoQuest, Onxerna, Regeneron, Roche/Genentech; Financial Interests, Personal, Other, participation on a data safety monitoring board or advisory board: Eisai/BMS, VBL Therapeutics. M.R. Mirza: Financial Interests, Institutional, Research Grant: Allarity, Apexigen, AstraZeneca, Boehringer Ingelheim, Clovis, GSK, Novartis, Ultimovacs; Financial Interests, Personal, Other, trial chair: Deciphera, Mersana, NuvationBio; Financial Interests, Personal, Invited Speaker: AstraZeneca, GenMab, GSK, Mersana, Seagen, Takeda; Financial Interests, Personal, Member of Board of Directors, and holds stocks and shares: Karyopharm, Sera Prognostics. All other authors have declared no conflicts of interest.

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