KEYNOTE-859: 4.5-year median follow-up of pembrolizumab plus chemotherapy for previously untreated advanced HER2-negative gastric or gastroesophageal junction (G/GEJ) adenocarcinoma.
Abstract
4036 Background: In the phase 3KEYNOTE-859 study (NCT03675737), first-linepembrolizumab (pembro) + chemotherapy (chemo) continued to provide longer OS (HR, 0.79; 95% CI, 0.71-0.88) and PFS (HR, 0.76; 95% CI, 0.68-0.85), and a higher ORR (51.0% vs 42.0%) vs placebo + chemo in participants (pts) with HER2-negative G/GEJ adenocarcinoma, after a median follow-up of 41.6 mo (August 22, 2023). We present results after an additional 13 mo of follow-up. Methods: Eligible pts with untreated locally advanced or metastatic HER2-negative G/GEJ adenocarcinoma with PD-L1 status, measurable disease, and ECOG PS 0 or 1 were randomly assigned 1:1 to receive pembro 200 mg or placebo IV Q3W for ≤35 cycles + investigator’s choice of chemo (5-FU + cisplatin [FP] vs capecitabine + oxaliplatin [CAPOX]). The primary end point was OS. Secondary end points included PFS, ORR, and DOR, all per RECIST v1.1 by BICR, and safety. The data cutoff was September 27, 2024. Results: Median follow-up was 54.8 mo (Q1-Q3, 46.8-62.1). In all randomly assigned pts in the intention-to-treat population (N = 1579), median OS was 12.9 mo (95% CI, 11.9-14.0) for pembro + chemo vs 11.5 mo (95% CI, 10.6-12.1) for placebo + chemo (HR, 0.78; 95% CI, 0.70-0.86). In pts with PD-L1 CPS ≥1, median OS was 13.0 mo (95% CI, 11.6-14.2) vs 11.4 mo (95% CI, 10.5-12.0; HR, 0.74 [95% CI, 0.66-0.84]). In pts with PD-L1 CPS ≥10, median OS was 15.8 mo (95% CI, 14.0-19.3) vs 11.8 mo (95% CI, 10.3-12.7; HR, 0.64 [95% CI, 0.53-0.77]). PFS, ORR, and DOR were also consistent between the intention-to-treat population and pts with PD-L1 CPS ≥1 and PD-L1 CPS ≥10 (Table). Treatment-related AEs were reported in 751 pts (95.7%; grade 3-5, 466 [59.4%]) for pembro + chemo and 736 (93.5%; grade 3-5, 404 [51.3%]) for placebo + chemo. Conclusions: Pembro + chemo continued to show improved OS, PFS, and ORR vs placebo + chemo after a median study follow-up of 54.8 mo, regardless of PD-L1 status. The findings further support pembro + chemo as a first-line treatment option for locally advanced or metastatic HER2-negative G/GEJ adenocarcinoma. Clinical trial information: NCT03675737 . All ptsN = 1579 PD-L1 CPS ≥1n = 1235 PD-L1 CPS ≥10n = 553 Pembro + chemo n = 790 Pbo + chemo n = 789 Pembro + chemo n = 618 Pbo + chemo n = 617 Pembro + chemo n = 280 Pbo + chemo n = 273 OS, median (95% CI), mo 12.9 (11.9-14.0) 11.5 (10.6-12.1) 13.0 (11.6-14.2) 11.4 (10.5-12.0) 15.8 (14.0-19.3) 11.8 (10.3-12.7) HR (95% CI) 0.78 (0.70-0.86) 0.74 (0.66-0.84) 0.64 (0.53-0.77) PFS, median (95% CI), mo 6.9 (6.3-7.2) 5.6 (5.5-5.7) 6.9 (6.0-7.2) 5.6 (5.4-5.7) 7.8 (6.8-8.5) 5.6 (5.4-6.7) HR (95% CI) 0.76 (0.68-0.85) 0.72 (0.64-0.82) 0.62 (0.51-0.76) ORR, % (95% CI) 51.1 (47.6-54.7) 42.0 (38.5-45.5) 51.9 (47.9-55.9) 42.6 (38.7-46.6) 60.4 (54.4-66.1) 43.2 (37.3-49.3) DOR, median (range), mo 8.0(1.2+ to 66.3+) 5.7(1.3+ to 58.1+) 8.3(1.2+ to 66.3+) 5.6(1.3+ to 58.1+) 10.0(1.2+ to 66.3+) 5.7(1.4+ to 55.0+)
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (19)
Sun Young Rha
Lucjan Wyrwicz
Department of Oncology and Radiotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland
Patricio Eduardo Yanez Weber
Oncology-Hematology Unit, Department of Internal Medicine, School of Medicine, Universidad de la Frontera, Temuco, Chile
Yuxian Bai
Min-Hee Ryu
Asan Medical Center, Seoul, South Korea
Jeeyun Lee
Samsung Medical Center, Seoul, South Korea
Fernando Rivera
Medical Oncology Department, Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain
Gustavo Vasconcelos Alves
Centro Integrado de Pesquisa em Oncologia, Hospital Nossa Senhora de Conceição, Porto Alegre, Brazil
Marcelo Garrido
Hemato-Oncology Department, SAGA Clinical Trial Center and Universidad Mayor, Santiago, Chile
Kai-Keen Shiu
Manuel González Fernández
Hemato Oncólogo, IMAT-Oncomedica, Montería, Colombia
Jin Li
Maeve Aine Lowery
Department of Medical Oncology, Trinity St. James Cancer Institute, Dublin, Ireland
Timuçin Çil
Adana City Education and Research Hospital, Adana Faculty of Medicine, University of Health Sciences, Adana, Turkey
Felipe José Silva Melo Cruz
Instituto Brasileiro de Controle do Câncer, São Paulo, Brazil
Do-Youn Oh
Division of Medical Oncology, Department of Internal Medicine, Seoul National University Hospital, and the Cancer Research Institute, Seoul National University College of Medicine, Seoul, South Korea
Pierre Leconte
MSD France, Puteaux, France
Pooja Bhagia
Merck & Co, Inc, Rahway, NJ
ShuKui Qin
1GI Cancer Center of Nanjing Tianyinshan Hospital, Chinese Pharmaceutical University (CPU), Nanjing, China