Investigation of synergistic effects in trials of combination therapies with immune-checkpoint inhibitors in advanced gastric or gastroesophageal junction cancer.

J Jun Okui (Department of Surgery, Keio University School of Medicine, Tokyo, Japan) K Kengo Nagashima S Satoru Matsuda (Department of Surgery, Keio University School of Medicine, Tokyo, Japan) Y Yasunori Sato H Hirofumi Kawakubo (Department of Surgery, Keio University School of Medicine, Tokyo, Japan) M Masashi Takeuchi (Department of Surgery, Keio University School of Medicine, Tokyo, Japan) K Kenro Hirata K Kai Tsugaru (Division of Gastroenterology and Hepatology, Keio University School of Medicine, Tokyo, Japan) S Shun Yamamoto M Motoo Nomura T Takahiro Tsushima (Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka, Japan) H Hiroya Takeuchi K Ken Kato (Institute for Protein Research, The University of Osaka, 3-2 Yamadaoka, Suita-shi, Osaka 565-0871, Japan) Y Yuko Kitagawa

Abstract

405 Background: Combinations of immune checkpoint inhibitors (ICI) and chemotherapy (CT) have been approved for gastric cancer. However, there is a hypothesis that this combination may blunt antitumor immune responses because most chemotherapeutic agents also target lymphocytes. The primary objective was to investigate that the ICI and CT does not interfere each other’s therapeutic effects in advanced gastric cancer (GC) or gastroesophageal junction cancer (GEJC) patients. Methods: The reconstructed individual patient data was electronically extracted from the Kaplan-Meier curve of phase III randomized controlled trials (RCTs). The observed PFS curve of each constituent monotherapies was used to estimate simulated PFS curves expected under a model of independent drug action. If the observed curve demonstrated significantly better PFS than simulated curve, the combination of ICI and CT may have a synergistic effect, implying a superior outcome compared to simply adding the component monotherapy. Results: The study included 2,538 unresectable advanced, recurrent, or metastatic GC or GEJC patients from three RCTs comparing pembrolizumab (KEYNOTE-061, KEYNOTE-062 and KEYNOTE-859). In patients with programmed cell death ligand 1 (PD-L1) combined positive score (CPS) of 1 or greater, the 1-year and median PFS of the observed and simulated curves were 28.0% vs. 27.9%, and 6.89 months vs. 6.88 months, respectively. One sample log-rank test showed no significant differences between the observed and simulated curves (p = 0.107). In the subgroups with PD-L1 CPS ≥10 or <1, the 1-year PFS of the observed and simulated curves was 34.7% vs 32.8%, and 28.5% vs 26.8%. Conclusions: The observed PFS of ICT involving pembrolizumab was comparable to the simulated PFS estimated from the data for each monotherapy regardless of the magnitude of PD-L1 CPS. Although it was not clear whether potential synergies existed for ICT, these findings at least suggest that the benefits of ICI and CT are not interfering each other, thereby providing theoretical support for the efficacy of ICT in patients with advanced GC or GEJC.

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 405-405
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (14)

J

Jun Okui

Department of Surgery, Keio University School of Medicine, Tokyo, Japan

K

Kengo Nagashima

S

Satoru Matsuda

Department of Surgery, Keio University School of Medicine, Tokyo, Japan

Y

Yasunori Sato

H

Hirofumi Kawakubo

Department of Surgery, Keio University School of Medicine, Tokyo, Japan

M

Masashi Takeuchi

Department of Surgery, Keio University School of Medicine, Tokyo, Japan

K

Kenro Hirata

K

Kai Tsugaru

Division of Gastroenterology and Hepatology, Keio University School of Medicine, Tokyo, Japan

S

Shun Yamamoto

M

Motoo Nomura

T

Takahiro Tsushima

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka, Japan

H

Hiroya Takeuchi

K

Ken Kato

Institute for Protein Research, The University of Osaka, 3-2 Yamadaoka, Suita-shi, Osaka 565-0871, Japan

Y

Yuko Kitagawa