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Neoadjuvant docetaxel, oxaliplatin plus capecitabine versus oxaliplatin plus capecitabine phase III randomized controlled clinical trial for patients with locally advanced gastric adenocarcinoma: long-term results of a randomised controlled trial

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机构: [1]The Third Department of Surgery, the Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, China [2]Hebei Key Laboratory of Precision Diagnosis and Comprehensive Treatment of Gastric Cancer, Shijiazhuang 050011, China [3]Department of Pathology, the Fourth Hospital of Hebei Medical University, Shijiazhuang, 050011, China [4]Department of Endoscopy, the Fourth Hospital of Hebei Medical University, Shijiazhuang, 050011, China
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关键词: advanced gastric cancer capecitabine docetaxel oxaliplatin neoadjuvant chemotherapy pathological complete response prognosis

摘要:
Neoadjuvant chemotherapy with docetaxel, oxaliplatin, and capecitabine (DOX regimen) is rarely used in Eastern countries and its efficacy and safety in advanced gastric cancer have not been reported. In this open-label, randomized, controlled trial, the authors aimed to assess the clinical efficacy of neoadjuvant chemotherapy using the DOX and oxaliplatin plus capecitabine (XELOX) regimens, in comparison to surgery alone.Three hundred patients younger than 60 years with potentially resectable advanced gastric cancer (cT3-4, Nany, M0) were enrolled in this randomized controlled clinical trial between November 2014 and June 2018. The primary endpoint of the study was the pathological complete response (pCR) rate. Secondary endpoints included 3-year overall survival (OS), 3-year disease-free survival.In total, 280 patients (93 in the DOX group, 92 in the XELOX group, and 95 in the surgery group) were included in the per-protocol analysis. The DOX group demonstrated a significantly higher pCR rate compared to the XELOX group (16.1 vs. 4.3%, P=0.008). For patients with intestinal type, the DOX group exhibited significantly higher rates of both pCR and major pathological response compared to the XELOX group (P=0.007, P<0.001). The 3-year OS rates of the DOX group, the XELOX group and the surgery group were 56.9, 44.6, and 34.7%, respectively. The 3-year disease-free survival rates were 45.2, 40.2, and 28.4%, respectively. The neoadjuvant DOX regimen demonstrated a significant improvement in the 3-year OS of patients compared to the neoadjuvant XELOX regimen (P=0.037).The neoadjuvant DOX regimen has shown the potential to increase the pCR rate and improve the prognosis of patients with advanced gastric cancer who are under 60 years old.Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc.

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大类 | 2 区 医学
小类 | 2 区 外科
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大类 | 2 区 医学
小类 | 2 区 外科
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Q1 SURGERY
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Q1 SURGERY

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第一作者机构: [1]The Third Department of Surgery, the Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, China [2]Hebei Key Laboratory of Precision Diagnosis and Comprehensive Treatment of Gastric Cancer, Shijiazhuang 050011, China
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通讯机构: [1]The Third Department of Surgery, the Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, China [2]Hebei Key Laboratory of Precision Diagnosis and Comprehensive Treatment of Gastric Cancer, Shijiazhuang 050011, China
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