Phase II Study (NO LIMIT, WJOG13320G) of First-Line Nivolumab Plus Low-Dose Ipilimumab for Microsatellite Instability–High Advanced Gastric or Esophagogastric Junction Cancer
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
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (18)
Hisato Kawakami
Shigenori Kadowaki
Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan
Akitaka Makiyama
Masahiro Tsuda
Kenro Hirata
Naotoshi Sugimoto
Osaka International Cancer Institute, Osaka, Japan
Nozomu Machida
Hiroki Hara
Saitama Cancer Center, Ina, Japan
Hidekazu Hirano
Taito Esaki
National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan
Yoshito Komatsu
Shuichi Hironaka
Department of Medical Oncology, Kyorin University Faculty of Medicine, Tokyo, Japan
Yukari Kobayashi
Department of Immunology, Kindai University Faculty of Medicine, Osaka-sayama, Japan
Kazuhiro Kakimi
Yasutaka Chiba
Clinical Research Center, Kindai University Hospital, Osaka, Japan
Narikazu Boku
Ichinosuke Hyodo
NHO Shikoku Cancer Center, Matsuyama-Shi, Japan
Kei Muro
Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan