...
首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Phase I study of preoperative radiation therapy with concurrent infusional 5-fluorouracil and oxaliplatin followed by surgery and postoperative 5-fluorouracil plus leucovorin for T3/T4 rectal adenocarcinoma: ECOG E1297.
【24h】

Phase I study of preoperative radiation therapy with concurrent infusional 5-fluorouracil and oxaliplatin followed by surgery and postoperative 5-fluorouracil plus leucovorin for T3/T4 rectal adenocarcinoma: ECOG E1297.

机译:I期研究:术前放疗并用5-氟尿嘧啶和奥沙利铂同时输注,然后进行手术以及术后5-氟尿嘧啶加亚叶酸钙治疗T3 / T4直肠腺癌:ECOG E1297。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

PURPOSE: Oxaliplatin is a platinum analog and radiosensitizer active in colorectal cancer. We performed a Phase I trial to test the safety and preliminary efficacy of adding oxaliplatin to standard preoperative chemoradiation therapy for rectal cancer. METHODS AND MATERIALS: Eligible patients had T3 to T4 rectal adenocarcinoma. Patients received standard-dose radiation (50.4 Gy for 5.5 weeks) with concurrent infused 5-fluorouracil (5-FU) at 200 mg/m2 per day, 7 days per week. Oxaliplatin was given three times at 14-day intervals at 55, 70, or 85 mg/m2 during the 5.5-week radiation period, before resection. Adjuvant therapy consisted of four cycles of 5-FU (500 mg/m2 per week) with leucovorin (500 mg/m2 per week) given every 6 weeks. The main goals were to identify the maximum tolerated dose of oxaliplatin and the dose-limiting toxicities when given with 5-FU and RT. Secondary goals were to determine resectability, pathologic response, sphincter preservation, and overall survival rates. RESULTS: Twenty-one patients were enrolled, 5 at the 55 mg/m2 oxaliplatin dose level, 5 at 70 mg/m2, and 11 at 85 mg/m2. All patients were able to complete the preoperative chemoradiation regimen with no dose adjustments. No dose-limiting toxicities or differences in the type or extent of toxicity were noted among the groups. Nineteen patients underwent surgery (three abdominopelvic resections and 16 low anterior resections), for an 84% sphincter preservation rate. The pathologic complete response rate was 26% (5 patients), and minimal microscopic residual tumor was found in 21% (4 additional patients). CONCLUSIONS: Oxaliplatin was well tolerated at 85 mg/m2 given every 2 weeks in combination with standard preoperative chemoradiation for rectal cancer. The rates of major pathologic response and sphincter preservation are promising.
机译:目的:奥沙利铂是一种铂类类似物,对大肠癌具有放射增敏作用。我们进行了一项I期试验,以测试将奥沙利铂添加到直肠癌的标准术前化学放疗中的安全性和初步疗效。方法和材料:符合条件的患者患有T3至T4直肠腺癌。患者接受标准剂量的放射治疗(5.5周为50.4 Gy),同时每周7天每天200 mg / m2的剂量同时输注5-氟尿嘧啶(5-FU)。在切除前的5.5周放疗期间,以14、55、70或85 mg / m2的间隔每14天给予奥沙利铂3次。辅助治疗包括四个周期的5-FU(每周500 mg / m2)和亚叶酸(每周500 mg / m2),每6周一次。主要目标是确定使用5-FU和RT时奥沙利铂的最大耐受剂量和剂量限制毒性。次要目标是确定可切除性,病理反应,括约肌保存和总生存率。结果:招募了21名患者,奥沙利铂剂量水平为55 mg / m2的5名,70 mg / m2的5名和85 mg / m2的11名。所有患者无需调整剂量即可完成术前放化疗方案。各组之间均未发现剂量限制性毒性或毒性类型或程度的差异。 19例患者接受了手术(3例腹腔盆腔切除术和16例低位前切除术),保留了84%的括约肌。病理完全缓解率为26%(5例患者),在显微镜下观察到的微小残留肿瘤为21%(另外4例患者)。结论:奥沙利铂每2周给予85 mg / m2的耐受性,并结合标准的术前化学放射治疗直肠癌。主要病理反应和括约肌保留率是有希望的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号