The safety and efficacy of neoadjuvant immunochemotherapy following laparoscopic gastrectomy for gastric cancer: a multicenter Real-world clinical study

Author:

Sun Yu-Qin1234,Zhong Qing134,Lv Chen-Bin2,Zhu Ji-Yun5,Lin Guang-Tan134,Zhang Zhi-Quan134,Wu Dong134,Weng Cai-Ming134,Chen Qiu-Xian2,Lian Ming-Qiao2,Zeng Wei-Ming2,Zhang Yong-Bin2,Chen Qi-Yue134,Lin Jian-Xian134,Xie Jian-Wei134,Li Ping134,Zheng Chao-Hui134,Lu Jun134,Cai Li-Sheng2,Huang Chang-Ming134

Affiliation:

1. Department of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, China

2. Department of Gastrointestinal Surgery, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, China

3. Department of General Surgery, Fujian Medical University Union Hospital, Fuzhou, China

4. Key Laboratory of Ministry of Education of Gastrointestinal Cancer, Fujian Medical University, Fuzhou, China

5. Department of General Surgery, The First Affiliated Hospital of Ningbo University, Zhejiang, China

Abstract

Background: The safety and efficacy of neoadjuvant immunochemotherapy (nICT) for locally advanced gastric cancer (LAGC) remain controversial. Methods: Patients with LAGC who received either nICT or neoadjuvant chemotherapy (nCT) at 3 tertiary referral teaching hospitals in China between January 2016 and October 2022 were analysed. After propensity-score matching (PSM), comparing the radiological response, pathological response rate, perioperative outcomes, and early recurrence between the two groups. Results: After PSM, 585 patients were included, with 195 and 390 patients comprising the nICT and nCT groups, respectively. The nICT group exhibited a higher objective response rate (79.5% versus [vs.] 59.0%; P<0.001), pathological complete response rate (14.36% vs. 6.41%; P=0.002) and major pathological response rate (39.49% vs. 26.15%; P=0.001) compared with the nCT group. The incidence of surgical complications (17.44% vs. 16.15%, P=0.694) and proportion of perioperative textbook outcomes (80.0% vs. 81.0%; P=0.767) were similar in both groups. The nICT group had a significantly lower proportion of early recurrence than the nCT group (29.7% vs. 40.8%; P=0.047). Furthermore, the multivariable logistic analysis revealed that immunotherapy was an independent protective factor against early recurrence (odds ratio 0.62 [95% CI 0.41-0.92]; P=0.018). No significant difference was found in neoadjuvant therapy drug toxicity between the two groups (51.79% vs. 45.38%; P=0.143). Conclusions: Compared with nCT, nICT is safe and effective, which significantly enhanced objective and pathological response rates, and reduced the risk for early recurrence among patients with LAGC. Trial Registration: Clinical Trials.gov.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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