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

Author:

Yukami Hiroki12ORCID,Kawazoe Akihito1ORCID,Lin Yi-Tzu34ORCID,Koyama Shohei3ORCID,Fukuoka Shota3ORCID,Hara Hiroki5ORCID,Takahashi Naoki5ORCID,Kojima Takashi1,Asayama Masako5,Yoshii Takako5,Bando Hideaki1ORCID,Kotani Daisuke1ORCID,Nakamura Yoshiaki1ORCID,Kuboki Yasutoshi1,Mishima Saori1ORCID,Wakabayashi Masashi6,Kuwata Takeshi7ORCID,Goto Masahiro8,Higuchi Kazuhide2,Yoshino Takayuki1ORCID,Doi Toshihiko1ORCID,Nishikawa Hiroyoshi3ORCID,Shitara Kohei149ORCID

Affiliation:

1. 1Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

2. 2The Second Department of Internal Medicine Center, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.

3. 3Division of Cancer Immunology, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center Hospital East, Kashiwa, Japan.

4. 4Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

5. 5Department of Gastroenterology, Saitama Cancer Center, Saitama, Japan.

6. 6Clinical Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.

7. 7Department of Pathology and Clinical Laboratories, National Cancer Center Hospital East, Kashiwa, Japan.

8. 8Cancer Chemotherapy Center, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.

9. 9Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Abstract

Abstract Purpose: 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. Patients and Methods: 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. Results: 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. Conclusions: 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.

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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