Phase II Study (NO LIMIT, WJOG13320G) of First-Line Nivolumab Plus Low-Dose Ipilimumab for Microsatellite Instability–High Advanced Gastric or Esophagogastric Junction Cancer

H Hisato Kawakami S Shigenori Kadowaki (Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan) A Akitaka Makiyama M Masahiro Tsuda K Kenro Hirata N Naotoshi Sugimoto (Osaka International Cancer Institute, Osaka, Japan) N Nozomu Machida H Hiroki Hara (Saitama Cancer Center, Ina, Japan) H Hidekazu Hirano T Taito Esaki (National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan) Y Yoshito Komatsu S Shuichi Hironaka (Department of Medical Oncology, Kyorin University Faculty of Medicine, Tokyo, Japan) Y Yukari Kobayashi (Department of Immunology, Kindai University Faculty of Medicine, Osaka-sayama, Japan) K Kazuhiro Kakimi Y Yasutaka Chiba (Clinical Research Center, Kindai University Hospital, Osaka, Japan) N Narikazu Boku I Ichinosuke Hyodo (NHO Shikoku Cancer Center, Matsuyama-Shi, Japan) K Kei Muro (Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan)

Abstract

PURPOSE Microsatellite instability–high (MSI-H) advanced gastric or esophagogastric junction cancer (AGC), accounting for 5%-6% of all AGC cases, has shown an enhanced responsiveness to immunotherapy. We performed a single-arm phase II study to evaluate the combination of nivolumab (NIVO) and low-dose (LD) ipilimumab (IPI) for first-line treatment of MSI-H AGC. PATIENTS AND METHODS Patients with MSI-H AGC received NIVO (240 mg once every 2 weeks) and IPI (1 mg/kg once every 6 weeks). The primary end point was overall response rate (ORR) assessed by blinded independent central review. Secondary end points included disease control rate (DCR), progression-free survival (PFS), overall survival (OS), safety, and biomarker analysis. MSI-H status was confirmed with an MSI-IVD Kit (Falco). RESULTS Twenty-nine patients were enrolled. The ORR was 62.1% (95% CI, 42.3 to 79.3), with a complete response rate of 10.3%. The DCR was 79.3% (95% CI, 60.3 to 92.0). Treatment-related adverse events (TRAEs) of any grade occurred in 93.1% of patients, with those of grade ≥3 manifesting in 37.9% of patients. At the data cutoff (median follow-up of 9.0 months), treatment had been discontinued in 21 patients, with such discontinuation being due to TRAEs in 12 (41.4%) patients. However, after exclusion of one patient with progressive disease, the remaining 11 patients showed long-term antitumor efficacy after treatment discontinuation (range of response duration, 0.9+ to 15.6+ months). The median PFS was 13.8 months (95% CI, 13.7 months to not reached [NR]) and the median OS was NR (95% CI, 13.7 months to NR), with a 12-month OS rate of 79.5%. CONCLUSION NIVO plus LD-IPI showed robust and durable antitumor efficacy as a first-line treatment for MSI-H AGC. Although TRAEs often led to treatment discontinuation, treatment efficacy was subsequently sustained in most patients.

Article Details

Volume / Issue Vol. 43, Issue 19
Published July 01, 2025
Pages 2184-2195
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (18)

H

Hisato Kawakami

S

Shigenori Kadowaki

Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan

A

Akitaka Makiyama

M

Masahiro Tsuda

K

Kenro Hirata

N

Naotoshi Sugimoto

Osaka International Cancer Institute, Osaka, Japan

N

Nozomu Machida

H

Hiroki Hara

Saitama Cancer Center, Ina, Japan

H

Hidekazu Hirano

T

Taito Esaki

National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan

Y

Yoshito Komatsu

S

Shuichi Hironaka

Department of Medical Oncology, Kyorin University Faculty of Medicine, Tokyo, Japan

Y

Yukari Kobayashi

Department of Immunology, Kindai University Faculty of Medicine, Osaka-sayama, Japan

K

Kazuhiro Kakimi

Y

Yasutaka Chiba

Clinical Research Center, Kindai University Hospital, Osaka, Japan

N

Narikazu Boku

I

Ichinosuke Hyodo

NHO Shikoku Cancer Center, Matsuyama-Shi, Japan

K

Kei Muro

Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan