首页> 美国卫生研究院文献>Japanese Journal of Clinical Oncology >A Phase II/III randomized controlled trial comparing perioperative versus postoperative chemotherapy with mFOLFOX6 for lower rectal cancer with suspected lateral pelvic node metastasis: Japan Clinical Oncology Group Study JCOG1310 (PRECIOUS study)
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A Phase II/III randomized controlled trial comparing perioperative versus postoperative chemotherapy with mFOLFOX6 for lower rectal cancer with suspected lateral pelvic node metastasis: Japan Clinical Oncology Group Study JCOG1310 (PRECIOUS study)

机译:II / III期随机对照试验比较了使用mFOLFOX6进行围手术期化疗与术后化疗与可疑盆腔外侧转移的下直肠癌的比较:日本临床肿瘤学小组研究JCOG1310(PRE​​CIOUS研究)

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摘要

A randomized phase II/III trial was started in May 2015 comparing perioperative versus postoperative chemotherapy with modified infusional fluorouracil and folinic acid with oxaliplatin for lower rectal cancer patients with suspected lateral pelvic node metastasis. The standard arm is total mesorectal excision or tumor-specific mesorectal excision with lateral pelvic node dissection (LND) followed by postoperative chemotherapy (modified infusional fluorouracil and folinic acid with oxaliplatin; 12 cycles). The experimental (perioperative chemotherapy) arm is six courses of modified infusional fluorouracil and folinic acid with oxaliplatin before and six courses after total mesorectal excision with lateral pelvic node dissection. The aim of this trial is to confirm the superiority of perioperative chemotherapy. A total of 330 patients will be enrolled over 7 years. The primary endpoint in Phase II part is proportion of R0 resection and that in Phase III part is overall survival. Secondary endpoints are progression-free survival, local progression-free survival, etc. This trial has been registered in the UMIN Clinical Trials Registry as UMIN000017603 [].
机译:2015年5月开始了一项II / III期随机试验,比较了怀疑有盆腔外侧结节转移的下直肠癌患者围手术期化疗与术后化疗加氟尿嘧啶和亚叶酸联合奥沙利铂的疗效。标准组为全直肠系膜切除术或肿瘤特异性直肠系膜切除术及盆腔外侧淋巴结清扫术(LND),然后进行术后化疗(改良输注氟尿嘧啶和亚叶酸与奥沙利铂; 12个周期)。实验组(围手术期化疗)是在全直肠系膜全切除并伴有骨盆外侧淋巴结清扫术之前和之后的六个疗程,分别是六个疗程的改良输注氟尿嘧啶和亚叶酸加奥沙利铂。该试验的目的是确认围手术期化疗的优越性。 7年内将总共招募330名患者。第二阶段的主要终点是R0切除的比例,第三阶段的主要终点是总体存活率。次要终点是无进展生存期,局部无进展生存期等。该试验已在UMIN临床试验注册中心注册为UMIN000017603 []。

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