Yoshida Yoichiro, Aisu Naoya, Kojima Daibo, Mera Toshiyuki, Kiyomi Fumiaki, Yamashita Yuichi, Hasegawa Suguru
Department of Gastroenterological Surgery Fukuoka University Faculty of Medicine Fukuoka Japan.
Academia Industry and Government Collaborative Research Institute of Translational Medicine for Life Innovation Fukuoka University Fukuoka Japan.
Ann Gastroenterol Surg. 2017 Aug 14;1(3):219-225. doi: 10.1002/ags3.12023. eCollection 2017 Sep.
Initiating chemotherapy usually requires a delay of more than 4 weeks after surgically resecting colorectal cancer. However, there is little evidence regarding the required delay interval. We have previously reported a pilot study to determine the safety and feasibility of early initiation of chemotherapy after resecting primary colorectal cancer with distant metastases. We aimed to determine the safety and efficacy of early initiation of chemotherapy after resecting colorectal cancer with distant metastases. This phase II study (trial number UMIN000006310) was a prospective, single-arm trial. A total of 20 patients (men, 15 and women, 5) were enrolled. They underwent XELOX therapy (130 mg/m oxaliplatin on day 1+1000 mg/m capecitabine twice daily on days 1-4) on postoperative day 7 and XELOX+bevacizumab (7.5 mg/kg bevacizumab on day 1) after the second chemotherapy cycle. Baseline characteristics included a median age of 64 (range, 43-72) years. Surgical procedures included right hemicolectomy in six patients, sigmoidectomy in three, anterior resection in five, and Hartmann procedure in six. All patients started chemotherapy on postoperative day 7. Median progression-free survival was 14.9 months; overall response rate was 80%. Disease control rate was 100%. Grade 3 or higher hemotoxicity and grade 3 or higher non-hematological toxicity was noted in 5.0% and 25.0% of patients, respectively. Postoperative complications were observed in two patients (superficial incisional surgical site infection and ileus). Early initiation of chemotherapy after surgery is feasible. These findings suggest future changes of the start time of chemotherapy after surgery.
启动化疗通常需要在结直肠癌手术切除后延迟4周以上。然而,关于所需延迟间隔的证据很少。我们之前报道了一项初步研究,以确定在切除伴有远处转移的原发性结直肠癌后早期启动化疗的安全性和可行性。我们旨在确定在切除伴有远处转移的结直肠癌后早期启动化疗的安全性和疗效。这项II期研究(试验编号UMIN000006310)是一项前瞻性单臂试验。共纳入20例患者(男性15例,女性5例)。他们在术后第7天接受XELOX治疗(第1天给予130mg/m²奥沙利铂 + 第1 - 4天每天两次给予1000mg/m²卡培他滨),并在第二个化疗周期后接受XELOX + 贝伐单抗治疗(第1天给予7.5mg/kg贝伐单抗)。基线特征包括中位年龄64岁(范围43 - 72岁)。手术方式包括6例右半结肠切除术、3例乙状结肠切除术、5例前切除术和6例Hartmann手术。所有患者均在术后第7天开始化疗。中位无进展生存期为14.9个月;总缓解率为80%。疾病控制率为100%。分别有5.0%和25.0%的患者出现3级或更高等级的血液毒性和3级或更高等级的非血液学毒性。两名患者出现术后并发症(浅表手术切口感染和肠梗阻)。术后早期启动化疗是可行的。这些发现提示了术后化疗开始时间的未来变化。