首页> 外文期刊>Japanese journal of clinical oncology. >Phase III trial to confirm the superiority of pelvic and para-aortic lymphadenectomy to pelvic lymphadenectomy alone for endometrial cancer: Japan Clinical Oncology Group Study 1412 (SEPAL-P3)
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Phase III trial to confirm the superiority of pelvic and para-aortic lymphadenectomy to pelvic lymphadenectomy alone for endometrial cancer: Japan Clinical Oncology Group Study 1412 (SEPAL-P3)

机译:III期试验,以确认骨盆和帕拉 - 主动脉淋巴结切除术的优越性对单独的骨盆淋巴结切除术进行子宫内膜癌:日本临床肿瘤学群体研究1412(Sepal-P3)

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To prospectively investigate the survival benefit of para-aortic lymphadenectomy, we launched a new study, the JCOG1412. This is a randomized Phase III trial to confirm the superiority of pelvic and para-aortic lymphadenectomy to pelvic lymphadenectomy alone. Patients corresponding to possible FIGO Stage IB, II, IIIA, IIIB, and a part of IIIC1 are eligible for the first registration before surgery. Next, those patients without evidence of para-aortic lymph node metastasis and multiple pelvic lymph node metastasis during surgery will be included in the second registration and randomized to either the pelvic lymphadenectomy alone arm or the pelvic and para-aortic lymphadenectomy arm. After the initial surgery, patients with post-operative recurrence risks receive adjuvant chemotherapy. The primary endpoint is overall survival. Secondary endpoints include relapse-free survival, short-term surgical outcomes, adverse events related to adjuvant chemotherapy and recurrence patterns. This trial has been registered at the UMIN Clinical Trials Registry [http://www.umin.ac.jp/ctr/index.htm] as UMIN000025399.
机译:为了前瞻性地调查Para-主动脉淋巴结切除术的生存效果,我们推出了新的研究,JCOG1412。这是一项随机阶段III试验,以确认单独对盆腔淋巴结切除术的骨盆和对齐淋巴结切除术的优越性。对应于可能的Figo Stage IB,II,IIIA,IIIB和IIIC1的一部分的患者有资格在手术前首次注册。接下来,在术中没有证据表明手术期间的患者和多个盆腔淋巴结转移的患者将包括在第二个注册中,并随机分配给盆腔淋巴结切除单独臂或盆腔和对准淋巴结切除术。初步手术后,术后复发风险患者接受佐剂化疗。主要终点是整体存活率。次要终点包括无复发存活,短期手术结果,与佐剂化疗和复发模式相关的不良事件。该试验已在UMIN临床试验登记处注册[http://www.umb.ac.jp/ctr/index.htm],如umin000025399。

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