Department of Radiotherapy II, M. Sklodowska-Curie Memorial Cancer Centre, Warsaw, Poland.
Radiother Oncol. 2013 May;107(2):171-7. doi: 10.1016/j.radonc.2013.03.001. Epub 2013 Apr 13.
To present an interim analysis of the trial comparing two neoadjuvant therapies for unresectable rectal cancer.
Patients with fixed cT3 or cT4 or locally recurrent rectal cancer without distant metastases were randomized to either 5 × 5 Gy and 3 courses of FOLFOX4 (schedule I) or 50.4 Gy delivered in 28 fractions given simultaneously with 5-Fu, leucovorin and oxaliplatin (schedule II). Surgery in both groups was performed 12 weeks after the beginning of radiation and 6 weeks after neoadjuvant treatment.
49 patients were treated according to schedule I and 48 according to schedule II. Grade III+ acute toxicity was observed in 26% of patients in group I and in 25% in group II. There were two toxic deaths, both in group II. The microscopically radical resection (primary endpoint) rate was 73% in group I and 71% in group II. Overall and severe postoperative complications were recorded in 27% and 9% of patients vs. 16% and 7%, respectively. Pathological complete response was observed in 21% of the patients in group I and in 9% in group II.
The interim analysis revealed no major differences in acute toxicity and local efficacy between the two evaluated strategies.
介绍比较两种不可切除直肠癌新辅助治疗方法的试验的中期分析结果。
无远处转移的固定 cT3 或 cT4 或局部复发性直肠癌患者随机分为两组,分别接受 5×5 Gy 和 3 个疗程的 FOLFOX4(方案 I)或 50.4 Gy 分 28 次给予,同时给予 5-Fu、亚叶酸钙和奥沙利铂(方案 II)。两组患者均在放疗开始后 12 周和新辅助治疗后 6 周进行手术。
49 例患者按方案 I 治疗,48 例患者按方案 II 治疗。I 组中 26%的患者出现 3 级以上急性毒性,II 组中 25%的患者出现急性毒性。两组均有 2 例毒性死亡。显微镜下根治性切除率(主要终点)在 I 组为 73%,在 II 组为 71%。I 组和 II 组分别有 27%和 9%的患者出现总体和严重术后并发症,16%和 7%的患者出现术后并发症。I 组有 21%的患者出现病理完全缓解,II 组有 9%的患者出现病理完全缓解。
中期分析显示,两种评估策略的急性毒性和局部疗效之间没有显著差异。