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首页> 外文期刊>World Journal of Surgical Oncology >Pilot study of the early start of chemotherapy after resection of primary colorectal cancer with distant metastases (Pearl Star 01)
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Pilot study of the early start of chemotherapy after resection of primary colorectal cancer with distant metastases (Pearl Star 01)

机译:原发性大肠癌伴远处转移切除术后早期化疗的初步研究(Pearl Star 01)

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Background The start of chemotherapy usually requires a delay of about 4 weeks after surgical resection of colorectal cancer. However, there is no evidence for the required length of this delay interval. In addition, there is a chance that a patient may die because postoperative chemotherapy was not started soon enough and a metastatic tumor was able to develop rapidly. We therefore conducted a pilot study to determine the safety and feasibility of an early start of chemotherapy after the resection of colorectal cancer with distant metastases. Methods Five patients were enrolled. They received XELOX therapy (130 mg/m2 of oxaliplatin on day 1 plus 1,000 mg/m2 of capecitabine twice daily on days 1 to 14) on the 7th postoperative day and XELOX + bevacizumab (7.5 mg/kg of bevacizumab on day 1) after the 2nd cycle of chemotherapy. Results Five patients underwent open surgery. The procedures included right hemicolectomy in 1 patient, sigmoidectomy in 2 patients, high anterior resection in 1 patient, and Hartmann procedure in 1 patient. All patients started chemotherapy on postoperative day 7. The median number of cycles of chemotherapy was 11 (8 to 22). No postoperative complications were observed. The tumor reduction rate was 44.3% (32.0 to 66.6%). Progression-free survival was 10.3 months. Conclusions An early start of chemotherapy after surgery is feasible and safe. These findings suggest possible changes in the start time of chemotherapy after surgery in the future. We have already started a new phase II trial to confirm the effects of the early start of chemotherapy after surgery. Trial registration UMIN000004361.
机译:背景化学疗法的开始通常需要在结直肠癌的外科手术切除后延迟约4周。但是,没有证据表明此延迟间隔的所需长度。另外,由于术后化疗还没有开始得太早,并且转移性肿瘤能够迅速发展,患者可能会死亡。因此,我们进行了一项初步研究,以确定切除远处转移的大肠癌后早期开始化疗的安全性和可行性。方法招募5例患者。他们在术后第7天接受XELOX疗法(第1天130 mg / m2的奥沙利铂加第1至14天每天两次1000 mg / m2的卡培他滨),并在术后第7天接受XELOX +贝伐单抗(7.5 mg / kg贝伐单抗)。化疗的第二个周期。结果5例患者接受了开放手术。手术包括右半结肠切除术1例,乙状结肠切除术2例,高位前切除术1例和Hartmann手术1例。所有患者均在术后第7天开始化疗。化疗的中位周期数为11(8至22)。没有观察到术后并发症。肿瘤减少率为44.3%(32.0%至66.6%)。无进展生存期为10.3个月。结论术后早期开始化疗是可行且安全的。这些发现表明将来手术后化学疗法的开始时间可能发生变化。我们已经开始了一项新的II期试验,以确认术后早期开始化疗的效果。试用注册UMIN000004361。

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