Major pathologic response as a prognostic surrogate in esophageal squamous cell carcinoma patients receiving neoadjuvant chemotherapy/ chemoimmunotherapy: A multi-center cohort study

被引:2
作者
Hong, Zhinuan [1 ,2 ,3 ,4 ]
Xie, Shuhan [1 ,2 ,3 ,4 ]
Xu, Hui [1 ,2 ,3 ,4 ]
Ke, Sunkui [5 ]
Liu, Wenyi [7 ,8 ]
Huang, Shijie [6 ]
Chen, Shuchen [1 ,2 ,3 ,4 ,6 ]
Xie, Jinbiao [6 ]
Xu, Jinxin [5 ]
Kang, Mingqiang [1 ,2 ,3 ,4 ]
机构
[1] Fujian Med Univ, Union Hosp, Dept Thorac Surg, Fuzhou, Peoples R China
[2] Fujian Med Univ, Fujian Prov Univ, Key Lab Cardiothorac Surg, Fuzhou, Peoples R China
[3] Fujian Med Univ, Key Lab Minist Educ Gastrointestinal Canc, Fuzhou, Peoples R China
[4] Fujian Med Univ, Fujian Key Lab Tumor Microbiol, Fuzhou, Peoples R China
[5] Xiamen Univ, Zhongshan Hosp, Sch Med, Dept Thorac Surg, Xiamen, Peoples R China
[6] Putian Univ, Affiliated Hosp, Dept Cardiothorac Surg, Putian, Peoples R China
[7] Chinese Acad Med Sci & Peking Union Med Coll, Natl Clin Res Ctr Canc, Natl Canc Ctr, Dept Thorac Surg,Canc Hosp, Shenzhen, Peoples R China
[8] Chinese Acad Med Sci & Peking Union Med Coll, Shenzhen Hosp, Shenzhen, Peoples R China
来源
EJSO | 2025年 / 51卷 / 02期
基金
中国国家自然科学基金;
关键词
Major pathologic response; Prognostic surrogate; Neoadjuvant; Chemoimmunotherapy; Neoadjuvant chemotherapy; Cancer recurrence patterns; Recurrence-free survival; CANCER; CHEMORADIOTHERAPY; SURVIVAL; IMMUNOTHERAPY; REGRESSION; PLACEBO;
D O I
10.1016/j.ejso.2024.109500
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the prognostic and survival surrogate value of major pathologic response (MPR) in esophageal squamous cell carcinoma (ESCC) patients undergoing neoadjuvant chemotherapy/chemoimmunotherapy(nCT/nICT) and surgery. Method: A retrospective multi-center study cohort study enrolled 305 ESCC patients who underwent neoadjuvant chemotherapy/chemoimmunotherapy followed by esophagectomy. Endpoints included recurrence-free survival (RFS), locoregional recurrence-free survival(L-RFS), distant metastasis-free survival(D-MFS), and recurrence patterns. The Cox regression analysis and Harrell's C-index were used to analyze survival differences and surrogate endpoints. The Kaplan-Meier method was used for the subgroup analysis in two subgroups(the patients receiving nICT and patients receiving nCT) and the prognostic value analysis of adjuvant therapy in non-MPR and MPR patients. Result: Of the 305 patients, 105 achieved MPR, demonstrating a significantly improved RFS (P value < 0.001), LRFS (P value < 0.001), and D-MFS (P value = 0.003). MPR was identified as an independent risk factor for RFS (HR:0.415, 95%CI:[0.227, 0.759], P value = 0.004) and demonstrated equal predictive capacity to be a surrogate of survival endpoints with T stage and N stage(Harrell's C-index: 0.613). In subgroup analysis, patients with MPR showed better survival outcomes in subgroups that received neoadjuvant chemoimmunotherapy (P value = 0.012) and neoadjuvant chemotherapy(P value < 0.001). Additionally, adjuvant therapy did not confer additional survival benefits to both MPR and non-MPR patients. Compared with patients who achieved MPR, nonMPR patients exhibited a higher recurrence rate, although the recurrence sites were similar between the two groups. Conclusion: MPR can serve as an independent prognostic factor and a surrogate of survival endpoints in ESCC patients undergoing nCT/nICT. Besides, as a potential indicator for postoperative management, MPR can provide reference basis and evidence support in clinical practice.
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页数:8
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