胸部 ESCC 患者的三野与两野淋巴结切除术:一项多中心随机研究(NST 1503)

IF 7.6 Q1 ONCOLOGY
Yousheng Mao , Shuoyan Liu , Yongtao Han , Shiping Guo , Chun Chen , Shugeng Gao , Anlin Hao , Hongbing Duan , Wentao Fang , Renquan Zhang , Zhentao Yu , Xiangning Fu , Xiaofei Li , Qun Wang , Lijie Tan , Zhigang Li , Yin Li , Zhirong Zhang , Wenqiang Wei , Yan Fang , Jie He
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引用次数: 0

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本文章由计算机程序翻译,如有差异,请以英文原文为准。
Three-field vs two-field lymphadenectomy in thoracic ESCC patients: a multicenter randomized study (NST 1503)

Background

3-field lymph node dissection (3FL) frequently lead to much more perioperative complications than 2-field lymph node dissection (2FL). This study was designed as a non-inferiority trial to evaluate whether 3FL could be omitted without compromising overall survival (OS) and disease-free survival (DFS) in the patients with resectable thoracic esophageal squamous cell cancer (ESCC) and negative right recurrent laryngeal nerve lymph nodes (RRLN-LNs).

Methods

cT1b-3N0–1M0 thoracic ESCC patients were managed in 3 arms during open or minimally invasive McKeown esophagectomy according to the results of frozen section examination for RRLN-LNs: if positive, direct 3FL (RRLN[+]-3FL); if negative, 2FL (RRLN[-]-2FL) or 3FL (RRLN[-]-3FL) by randomization.

Results

Based on frozen section, of the 829 finally recruited patients, 121 (13.6 %) had positive RRLN-LNs and direct 3FL (RRLN[+]-3FL); 766 had negative RRLN-LNs and were randomized into the RRLN [-]-2FL (386 cases) or RRLN[-]-3FL (380 cases) group. The cervical LN metastasis rate in the RRLN[+]-3FL group (28.9 %) was significantly higher than that in the RRLN[-]-3FL group (8.3 %) (P<0.001). The 5-year OS and DFS were 72.2 % and 65.1 % in the RRLN[-]-3FL group and 68.8 % and 62.8 % in the RRLN[-]-2FL group (OS, P = 0.163; DFS, P = 0.378), versus 50.3 % and 41.2 % in the RRLN[+]-3FL group (both P<0.001), respectively.

Conclusions

Additional cervical lymphadenectomy can be avoided in the patients with middle or lower thoracic ESCC and negative RRLN-LNs by frozen section treated by upfront surgery.
Trial Registration: ClinicalTrials.gov Identifier NCT02448953.
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