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A Phase II Trial of Combined Treatment of Endoscopic Mucosal Resection and Chemoradiotherapy for Clinical Stage I Esophageal Carcinoma: Japan Clinical Oncology Group Study JCOG0508

机译:内镜黏膜切除与化学放疗联合治疗I期食管癌的II期试验:日本临床肿瘤学小组研究JCOG0508

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摘要

Standard treatment for clinical stage I esophageal cancer with submucosal invasion (T1b) has been surgical resection. We conducted a Phase II trial to evaluate the efficacy and the safety of combined treatment of endoscopic mucosal resection (EMR) and chemoradiotherapy for clinical stage I (T1b) esophageal cancer. Patients diagnosed as having clinical stage I (T1b) esophageal cancer which is considered to be resectable by EMR are eligible. When pathological examination of the EMR specimen confirms T1b tumor with negative or positive resection margin, the patient undergoes chemoradiotherapy. The study continues until 82 patients with T1b tumor with negative resection margin are enrolled from 20 institutions. The primary endpoint is 3-year overall survival (OS) in pT1b cases with negative resection margin. The secondary endpoints are 3-year OS and progression-free survival in all eligible cases, OS in pT1a-MM cases with margin-negative, complications of EMR and adverse events of chemoradiotherapy. The data from this trial will be expected to provide a non-surgical treatment option to the patients with clinical stage I (T1b) esophageal cancer.
机译:具有粘膜下浸润(T1b)的临床I期食管癌的标准治疗方法是手术切除。我们进行了一项II期临床试验,以评估内镜黏膜切除术(EMR)与放化疗联合治疗I期(T1b)食管癌的疗效和安全性。被诊断患有I期(T1b)食管癌且被EMR切除的患者符合条件。当EMR标本的病理检查确定切除边缘为阴性或阳性的T1b肿瘤时,患者将接受放化疗。这项研究一直持续到从20个机构招募了82例切缘阴性的T1b肿瘤患者为止。主要终点是切除边缘阴性的pT1b病例的3年总生存期(OS)。次要终点为所有合格病例的3年OS和无进展生存期,pT1a-MM伴边缘阴性,EMR并发症和放化疗不良事件的OS。预计该试验的数据将为I期(T1b)食管癌患者提供非手术治疗选择。

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