Updated Efficacy Outcomes of Anti-PD-1 Antibodies plus Multikinase Inhibitors for Patients with Advanced Gastric Cancer with or without Liver Metastases in Clinical Trials.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
15 08 2022
Historique:
received: 27 02 2022
revised: 24 05 2022
accepted: 07 06 2022
pubmed: 10 6 2022
medline: 17 8 2022
entrez: 9 6 2022
Statut: ppublish

Résumé

We previously reported preliminary activity of regorafenib plus nivolumab (REGONIVO) or lenvatinib plus pembrolizumab (LENPEM) in advanced gastric cancer (AGC). Meanwhile, several studies demonstrated liver metastases are less responsive to immunotherapy. Combined efficacy outcomes with a longer follow-up in a phase Ib trial of REGONIVO and a phase II trial of LENPEM were examined in AGC with or without liver metastases (REGONIVO plus LENPEM cohort). We also investigated the efficacy of anti-PD-1 monotherapies (anti-PD-1 monotherapy cohort). A comparison of the immune microenvironment between gastric primary tumors and liver metastases was also conducted by multiplex IHC. In the REGONIVO plus LENPEM cohort, with a median follow-up of 14.0 months, objective response rate (ORR), median progression-free survival (mPFS), and median overall survival (mOS) were 46%, 7.8 months, and 15.6 months in patients with liver metastases, while 69%, 6.9 months, and 15.5 months in those without. In the anti-PD-1 monotherapy cohort, with a median follow-up of 27.6 months, ORR, mPFS, and mOS were 9%, 1.4 months, and 6.4 months in patients with liver metastases, while 22%, 2.3 months, and 9.0 months in those without. Multiplex IHC revealed liver metastases were associated with an abundance of immune-suppressive cells, such as tumor-associated macrophages and regulatory T cells, with fewer CD8+ T cells compared with gastric primary tumors. Anti-PD-1 antibodies plus regorafenib or lenvatinib for AGC showed promising antitumor activity with a longer follow-up, irrespective of liver metastases status, despite a more immune-suppressive tumor microenvironment in liver metastases.

Identifiants

pubmed: 35679062
pii: 707383
doi: 10.1158/1078-0432.CCR-22-0630
pmc: PMC9662898
doi:

Substances chimiques

Nivolumab 31YO63LBSN

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3480-3488

Informations de copyright

©2022 The Authors; Published by the American Association for Cancer Research.

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Auteurs

Hiroki Yukami (H)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
The Second Department of Internal Medicine Center, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.

Akihito Kawazoe (A)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Yi-Tzu Lin (YT)

Division of Cancer Immunology, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center Hospital East, Kashiwa, Japan.
Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Shohei Koyama (S)

Division of Cancer Immunology, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center Hospital East, Kashiwa, Japan.

Shota Fukuoka (S)

Division of Cancer Immunology, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center Hospital East, Kashiwa, Japan.

Hiroki Hara (H)

Department of Gastroenterology, Saitama Cancer Center, Saitama, Japan.

Naoki Takahashi (N)

Department of Gastroenterology, Saitama Cancer Center, Saitama, Japan.

Takashi Kojima (T)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Masako Asayama (M)

Department of Gastroenterology, Saitama Cancer Center, Saitama, Japan.

Takako Yoshii (T)

Department of Gastroenterology, Saitama Cancer Center, Saitama, Japan.

Hideaki Bando (H)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Daisuke Kotani (D)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Yoshiaki Nakamura (Y)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Yasutoshi Kuboki (Y)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Saori Mishima (S)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Masashi Wakabayashi (M)

Clinical Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.

Takeshi Kuwata (T)

Department of Pathology and Clinical Laboratories, National Cancer Center Hospital East, Kashiwa, Japan.

Masahiro Goto (M)

Cancer Chemotherapy Center, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.

Kazuhide Higuchi (K)

The Second Department of Internal Medicine Center, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.

Takayuki Yoshino (T)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Toshihiko Doi (T)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Hiroyoshi Nishikawa (H)

Division of Cancer Immunology, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center Hospital East, Kashiwa, Japan.

Kohei Shitara (K)

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

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