Preoperative Chemoradiotherapy plus Nivolumab before Surgery in Patients with Microsatellite Stable and Microsatellite Instability–High Locally Advanced Rectal Cancer

Author:

Bando Hideaki1ORCID,Tsukada Yuichiro2ORCID,Inamori Koji23ORCID,Togashi Yosuke3ORCID,Koyama Shohei3,Kotani Daisuke1ORCID,Fukuoka Shota13,Yuki Satoshi4ORCID,Komatsu Yoshito5ORCID,Homma Shigenori6,Taketomi Akinobu6,Uemura Mamoru78,Kato Takeshi7ORCID,Fukui Makoto9,Wakabayashi Masashi9,Nakamura Naoki1011,Kojima Motohiro12ORCID,Kawachi Hiroshi13ORCID,Kirsch Richard14,Yoshida Tsutomu15,Suzuki Yutaka16,Sato Akihiro9,Nishikawa Hiroyoshi317ORCID,Ito Masaaki2,Yoshino Takayuki1ORCID

Affiliation:

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

2. 2Department of Colorectal Surgery, National Cancer Center Hospital East, Kashiwa, Japan.

3. 3Division of Cancer Immunology, Research Institute/Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Tokyo/Kashiwa, Japan.

4. 4Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan.

5. 5Department of Cancer Chemotherapy, Hokkaido University Hospital Cancer Center, Sapporo, Japan.

6. 6Department of Gastroenterological Surgery, Hokkaido University Hospital, Sapporo, Japan.

7. 7Department of Surgery, National Hospital Organization Osaka National Hospital, Osaka, Japan.

8. 8Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan.

9. 9Clinical Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.

10. 10Division of Radiation Oncology and Particle Therapy, National Cancer Center Hospital East, Kashiwa, Japan.

11. 11Department of Radiology, St. Marianna University Hospital, Kawasaki, Japan.

12. 12Division of Pathology, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center Hospital East, Kashiwa, Japan.

13. 13Department of Pathology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

14. 14Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada.

15. 15Department of Pathology, Kitasato University School of Medicine; Sagamihara, Japan.

16. 16Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Japan.

17. 17Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Abstract

Abstract Purpose: Preoperative chemoradiotherapy (CRT) and surgical resection are the standard treatment for locally advanced rectal cancer (LARC). Combining immune checkpoint inhibitors with radiation suggests a promising approach for enhancing efficacy. We investigated the efficacy of CRT followed by nivolumab and surgery in patients with LARC. Patients and Methods: In phase I, we investigated the feasibility of sequentially combined CRT, 5 cycles of nivolumab, and radical surgery. In phase II, patients with microsatellite stable (MSS) and microsatellite instability-high (MSI-H) LARC were evaluated. Results: Three patients in phase I received full courses of CRT and nivolumab without dose modification; the schedule was recommended for phase II. A pathologic complete response (pCR) was centrally confirmed in 30% [11/37; 90% confidence interval (CI), 18%–44%] and 60% (3/5) of the MSS and exploratory MSI-H cohorts, respectively. While immune-related severe adverse events were observed in 3 patients, no treatment-related deaths were observed. In 38 patients with MSS who underwent surgery, pCR rates of 75% (6/8) and 17% (5/30; P = 0.004, Fisher exact test) were observed in those with programmed cell death ligand 1 (PD-L1) tumor proportion score ≥1% and <1%, respectively; IHC staining was performed using pre-CRT samples. In 24 patients with MSS, pre-CRT samples were analyzed by flow cytometry; pCR rates of 78% (7/9) and 13% (2/15; P = 0.003, Fisher exact test) were observed for CD8+ T cell/effector regulatory T cell (CD8/eTreg) ratios of ≥2.5 and <2.5, respectively, in tumor-infiltrating lymphocytes. Conclusions: CRT followed by consolidation nivolumab could increase pCR. PD-L1 expression and an elevated CD8/eTreg ratio were positive predictors in patients with MSS LARC.

Funder

Ono Pharmaceutical

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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