首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Concurrent chemoradiotherapy with gemcitabine and cisplatin after incomplete (R1) resection of locally advanced pancreatic carcinoma.
【24h】

Concurrent chemoradiotherapy with gemcitabine and cisplatin after incomplete (R1) resection of locally advanced pancreatic carcinoma.

机译:局部晚期胰腺癌不完全切除后,吉西他滨和顺铂同时放化疗。

获取原文
获取原文并翻译 | 示例
           

摘要

PURPOSE: To analyze, in a prospective clinical trial, the efficacy and toxicity of concurrent radiotherapy and chemotherapy with gemcitabine and cisplatin in patients with incompletely (R1) resected pancreatic cancer. METHODS AND MATERIALS: Between 2000 and 2002, a total of 30 pancreatic cancer patients were treated. Radiotherapy was performed in 15 patients up to a total dose of 45.0 Gy. An additional 15 patients received a total dose of 50.0 Gy according to the International Commission on Radiation Units and Measurements (ICRU) Report 50 reference point (equivalent to 45.0 Gy at the isodose, including 90% covering the former tumor area and local lymph nodes). Concurrent with radiotherapy, four applications of gemcitabine (300 mg/m(2)) and cisplatin (30 mg/m(2)) were administered. After chemoradiotherapy, patients received four additional courses of gemcitabine (1000 mg/m(2)) and cisplatin (50 mg/m(2)) on Days 1 and 15 in a 4-week cycle. RESULTS: The median progression-free survival was 10.6 months, and the median overall survival was 22.8 months. The 1-, 2-, and 3-year survival rate was 81%, 43%, and 26%, respectively. After completion of chemoradiotherapy, distant metastasis was observed in 14 patients during a median follow-up of 15.0 months (range, 4.6-30.0). One patient developed both local recurrence and distant metastases. Hematologic toxicities were the most prominent side effects (leukopenia Grade 3 and 4 in 53% and 7% and thrombocytopenia Grade 3 and 4 in 33% and 7% of patients, respectively). Grade 3 and 4 GI toxicity was not observed. CONCLUSION: Postoperative chemoradiotherapy with gemcitabine and cisplatin after incomplete (R1) resection of pancreatic carcinoma is safe and feasible. A prolonged progression-free survival suggests high local efficacy, translating into a benefit of overall survival. On the basis of the favorable outcome of patients receiving gemcitabine/cisplatin-based chemoradiotherapy, testing this combined treatment strategy appears warranted in a comparative trial.
机译:目的:在一项前瞻性临床试验中,分析吉西他滨和顺铂同时放疗和化疗对未完全切除(R1)的胰腺癌患者的疗效和毒性。方法和材料:2000年至2002年,共治疗了30例胰腺癌患者。 15例患者接受了放射治疗,总剂量达到45.0 Gy。根据国际放射单位和测量委员会(ICRU)报告50参考点,另外15名患者接受了50.0 Gy的总剂量(相当于等剂量的45.0 Gy,其中90%覆盖了前肿瘤区域和局部淋巴结) 。与放疗同时,吉西他滨(300 mg / m(2))和顺铂(30 mg / m(2))的四次应用。化学放疗后,患者在第4天的第1天和第15天接受了另外四个疗程的吉西他滨(1000 mg / m(2))和顺铂(50 mg / m(2))。结果:中位无进展生存期为10.6个月,中位总体生存期为22.8个月。 1年,2年和3年生存率分别为81%,43%和26%。化学放疗完成后,在中位随访15.0个月(范围4.6-30.0)期间观察到14例患者远处转移。一名患者同时发生局部复发和远处转移。血液学毒性是最突出的副作用(分别在53%和7%的患者中出现白细胞减少3级和4级,在33%和7%的患者中出现血小板减少3级和4级)。没有观察到3级和4级GI毒性。结论:吉西他滨联合顺铂进行胰腺癌不完全切除术后放化疗是安全可行的。延长的无进展生存期表明较高的局部疗效,转化为总体生存期的益处。根据接受吉西他滨/顺铂为基础的放化疗患者的良好结果,在一项比较试验中似乎有必要测试这种联合治疗策略。

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