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

被引:105
作者
Bando, Hideaki [1 ]
Tsukada, Yuichiro [2 ]
Inamori, Koji [2 ,3 ]
Togashi, Yosuke [3 ]
Koyama, Shohei [3 ]
Kotani, Daisuke [1 ]
Fukuoka, Shota [1 ,3 ]
Yuki, Satoshi [4 ]
Komatsu, Yoshito [5 ]
Homma, Shigenori [6 ]
Taketomi, Akinobu [6 ]
Uemura, Mamoru [7 ,8 ]
Kato, Takeshi [7 ]
Fukui, Makoto [9 ]
Wakabayashi, Masashi [9 ]
Nakamura, Naoki [10 ,11 ]
Kojima, Motohiro [12 ]
Kawachi, Hiroshi [13 ]
Kirsch, Richard [14 ]
Yoshida, Tsutomu [15 ]
Suzuki, Yutaka [16 ]
Sato, Akihiro [9 ]
Nishikawa, Hiroyoshi [3 ,17 ]
Ito, Masaaki [2 ]
Yoshino, Takayuki [1 ]
机构
[1] Natl Canc Ctr Hosp East, Dept Gastroenterol & Gastrointestinal Oncol, 6-5-1 Kashiwanoha, Kashiwa, Chiba 2778577, Japan
[2] Natl Canc Ctr Hosp East, Dept Colorectal Surg, Kashiwa, Chiba, Japan
[3] Natl Canc Ctr, Exploratory Oncol Res & Clin Trial Ctr, Res Inst, Div Canc Immunol, Tokyo, Japan
[4] Hokkaido Univ Hosp, Dept Gastroenterol & Hepatol, Sapporo, Hokkaido, Japan
[5] Hokkaido Univ Hosp, Canc Ctr, Dept Canc Chemotherapy, Sapporo, Hokkaido, Japan
[6] Hokkaido Univ Hosp, Dept Gastroenterol Surg, Sapporo, Hokkaido, Japan
[7] Natl Hosp Org Osaka Natl Hosp, Dept Surg, Osaka, Japan
[8] Osaka Univ, Grad Sch Med, Dept Gastroenterol Surg, Osaka, Japan
[9] Natl Canc Ctr Hosp East, Clin Res Support Off, Kashiwa, Chiba, Japan
[10] Natl Canc Ctr Hosp East, Div Radiat Oncol & Particle Therapy, Kashiwa, Chiba, Japan
[11] St Marianna Univ Hosp, Dept Radiol, Kawasaki, Kanagawa, Japan
[12] Natl Canc Ctr Hosp East, Exploratory Oncol Res & Clin Trial Ctr, Div Pathol, Kashiwa, Chiba, Japan
[13] Japanese Fdn Canc Res, Canc Inst Hosp, Dept Pathol, Tokyo, Japan
[14] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON, Canada
[15] Kitasato Univ, Sch Med, Dept Pathol, Sagamihara, Kanagawa, Japan
[16] Univ Tokyo, Grad Sch Frontier Sci, Dept Computat Biol & Med Sci, Kashiwa, Chiba, Japan
[17] Nagoya Univ, Grad Sch Med, Dept Immunol, Nagoya, Aichi, Japan
关键词
REGULATORY T-CELLS; RADIATION-THERAPY; RADIOTHERAPY; BURDEN;
D O I
10.1158/1078-0432.CCR-21-3213
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 IL 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.
引用
收藏
页码:1136 / 1146
页数:11
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