Adjuvant therapy after neoadjuvant immunotherapy combined with chemotherapy in locally advanced resectable esophageal squamous cell carcinoma: A retrospective study study.
Abstract
e16152 Background : In esophageal squamous cell carcinoma (ESCC), neoadjuvant immunotherapy combined with chemotherapy followed by surgery (NICT+S) has shown good pathologic complete response rate (pCR) and prognosis. However, it is not known whether patients with ESCC who have received t also require adjuvant therapy. Methods: Data from 293 patients who received NICT+S between 2021 and 2023 were retrospectively analyzed. To compare disease-free survival (DFS) and overall survival (OS), we produced Kaplan-Meier survival curves. To determine the parameters associated with disease-free survival and overall survival, Cox models were developed using hazard ratios (HRs). Results: Among 293 ESCC patients who received NICT+S, 258 cases were ultimately included in the research. The percentage of R0 resection was 99.6%. After NICT, 62 (24.0%) patients achieved pathological complete response. Adjuvant therapy (AT) was given to 193 (74.8%) patients following NICT+S, 145 (56.2%) patients received adjuvant immunotherapy (AIT), 48 (18.6%) patients received adjuvant chemoradiotherapy (ACRT). There was no statistically significant difference between patients with and without AT in terms of 2-year DFS (78.7% vs. 75.7%, P = 0.68) or 2-year OS (94.9% vs. 90.5%, P = 0.28). Similarly in the presence or absence of AIT (2-year DFS: 76.9% vs. 75.7%, P = 0.877; 2-year OS: 94.5% vs. 90.5%, P = 0.337) and ACRT( 2-year DFS: 84.7% vs. 75.7%, P = 0.321; 2-year OS: 95.8% vs. 90.5%, P = 0.256), there was no statistical difference in survival outcomes. Patients with ypT 0-1 (P < 0.001, HR:0.34), ypN- (P < 0.001, HR:3.31), with T downing stage (P = 0.006, HR:2.68), and without underlying disease (P = 0.0362, HR:1.91), achieved better DFS with AT. Conclusions: The presence of AT had no significant survival benefit for patients with NICT+S. Patients with ypT 0-1, ypN-, T downing stage, and no underlying disease may benefit from AT.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (14)
Fangjie Ding
Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong, China
Yiming Mu
Wu Xue
Department of Orthopedics The Second Hospital of Jilin University Changchun China
Fengxue Li
Tulane University, New Orleans, Louisiana, United States
Xinquan Liang
Jining Medical University, Jining, Shandong, China
Pingping Hu
Yan Zhang
Fangjie Chen
Guodong Deng
The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, Shandong, China
Ning Liang
Jian Xie
Department of Pathology, Microbiology and Immunology, University of Nebraska Medical Center
Jiandong Zhang
Wuhan National Laboratory for Optoelectronics Huazhong University of Science and Technology Wuhan Hubei P. R. China
Lili Qiao
The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, Shandong, China
Yingying Zhang