Liu Ding-Xin, Li Dan-Dan, He Wan, Ke Chuan-Feng, Jiang Wu, Tang Jing-Hua, Kong Ling-Heng, Li Yuan, Sui Qiao-Qi, Xiao Bin-Yi, Li Wei-Rong, Hong Zhi-Gang, Xu Rui-Hua, Pan Zhi-Zhong, Zhang Xiao-Shi, Ding Pei-Rong
State Key Laboratory of Oncology in South China; Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Department of Colorectal Surgery, Sun Yat-sen University Cancer Center, Guangzhou, P.R. China.
Oncoimmunology. 2020 Jan 22;9(1):1711650. doi: 10.1080/2162402X.2020.1711650. eCollection 2020.
: Although PD-1 blockade has significantly improved the survival of metastatic colorectal cancer with DNA Mismatch Repair-Deficient/Microsatellite Instability-High (MSI-H), the data on neoadjuvant setting is limited. : In this retrospective study, we enrolled eight patients with advanced MSI-H colorectal cancer from three hospitals. Four patients are locally advanced and four are metastatic. All the patients received at least two doses of PD-1 antibody with or without chemotherapy as neoadjuvant therapy. The aim of the present study was to evaluate the short-term efficacy and toxicities of this strategy. : All the enrolled eight patients had a major response in imaging and/or pathological evaluation. Five of the seven resected patients were evaluated as pathological complete response. One patient without surgery has a clinical complete response (cCR) tumor response. : Neoadjuvant PD-1 blockade induced tumor regression with a major clinical and pathological response in advanced dMMR/MSI-H colorectal cancer. Further studies are required to evaluate the long-term effect of this strategy.
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