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.

S Sun Young Rha L Lucjan Wyrwicz (Department of Oncology and Radiotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland) P Patricio Eduardo Yanez Weber (Oncology-Hematology Unit, Department of Internal Medicine, School of Medicine, Universidad de la Frontera, Temuco, Chile) Y Yuxian Bai M Min-Hee Ryu (Asan Medical Center, Seoul, South Korea) J Jeeyun Lee (Samsung Medical Center, Seoul, South Korea) F Fernando Rivera (Medical Oncology Department, Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain) G Gustavo Vasconcelos Alves (Centro Integrado de Pesquisa em Oncologia, Hospital Nossa Senhora de Conceição, Porto Alegre, Brazil) M Marcelo Garrido (Hemato-Oncology Department, SAGA Clinical Trial Center and Universidad Mayor, Santiago, Chile) K Kai-Keen Shiu M Manuel González Fernández (Hemato Oncólogo, IMAT-Oncomedica, Montería, Colombia) J Jin Li M Maeve Aine Lowery (Department of Medical Oncology, Trinity St. James Cancer Institute, Dublin, Ireland) T Timuçin Çil (Adana City Education and Research Hospital, Adana Faculty of Medicine, University of Health Sciences, Adana, Turkey) F Felipe José Silva Melo Cruz (Instituto Brasileiro de Controle do Câncer, São Paulo, Brazil) D 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) P Pierre Leconte (MSD France, Puteaux, France) P Pooja Bhagia (Merck & Co, Inc, Rahway, NJ) S ShuKui Qin (1GI Cancer Center of Nanjing Tianyinshan Hospital, Chinese Pharmaceutical University (CPU), Nanjing, China)

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

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 4036-4036
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (19)

S

Sun Young Rha

L

Lucjan Wyrwicz

Department of Oncology and Radiotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland

P

Patricio Eduardo Yanez Weber

Oncology-Hematology Unit, Department of Internal Medicine, School of Medicine, Universidad de la Frontera, Temuco, Chile

Y

Yuxian Bai

M

Min-Hee Ryu

Asan Medical Center, Seoul, South Korea

J

Jeeyun Lee

Samsung Medical Center, Seoul, South Korea

F

Fernando Rivera

Medical Oncology Department, Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain

G

Gustavo Vasconcelos Alves

Centro Integrado de Pesquisa em Oncologia, Hospital Nossa Senhora de Conceição, Porto Alegre, Brazil

M

Marcelo Garrido

Hemato-Oncology Department, SAGA Clinical Trial Center and Universidad Mayor, Santiago, Chile

K

Kai-Keen Shiu

M

Manuel González Fernández

Hemato Oncólogo, IMAT-Oncomedica, Montería, Colombia

J

Jin Li

M

Maeve Aine Lowery

Department of Medical Oncology, Trinity St. James Cancer Institute, Dublin, Ireland

T

Timuçin Çil

Adana City Education and Research Hospital, Adana Faculty of Medicine, University of Health Sciences, Adana, Turkey

F

Felipe José Silva Melo Cruz

Instituto Brasileiro de Controle do Câncer, São Paulo, Brazil

D

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

P

Pierre Leconte

MSD France, Puteaux, France

P

Pooja Bhagia

Merck & Co, Inc, Rahway, NJ

S

ShuKui Qin

1GI Cancer Center of Nanjing Tianyinshan Hospital, Chinese Pharmaceutical University (CPU), Nanjing, China