首页> 外文期刊>Anti-cancer drugs >Phase II study of docetaxel in combination with oxaliplatin in patients with metastatic or locally advanced esophagogastric cancer previously untreated with chemotherapy for advanced disease: results of the Central European Cooperative Oncology Group
【24h】

Phase II study of docetaxel in combination with oxaliplatin in patients with metastatic or locally advanced esophagogastric cancer previously untreated with chemotherapy for advanced disease: results of the Central European Cooperative Oncology Group

机译:多西紫杉醇联合奥沙利铂在以前未经化疗治疗的晚期转移性或局部晚期食管胃癌患者中的II期研究:中欧合作肿瘤小组的结果

获取原文
获取原文并翻译 | 示例
           

摘要

A phase II trial was performed to determine the efficacy and tolerance of docetaxel plus oxaliplatin with hematopoietic growth factor support in previously untreated patients with advanced gastroesophageal adenocarcinoma. Thirty-five patients were entered in this trial. Treatment consisted of 3-weekly docetaxel 80 mg/m and oxaliplatin 100 mg/m both infused on day 1. A prophylactic 5-day course of human granulocyte colony-stimulating factor 5 mug/kg/day was given subcutaneously, and erythropoietin (10 000 IU subcutaneously three times per week) was administered if hemoglobin was less than 12.0 mg/dl. The confirmed overall response rate was 34%, including two complete responses (6%) and 10 partial responses (28%). Fifteen patients (43%) had stable disease. The median time to response was 2.5 months (1-3.5), the median time to progression was 8.9 (4-42.5) months and the median overall survival time was 11.6 (2.5-51) months. Hematologic toxicity was common, though World Health Organization grade 3 or 4 neutropenia occurred only in six (17%) patients and anemia in six (17%) patients, respectively. Nonhematologic adverse reactions were usually mild-to-moderate. Our data suggest that the combination of docetaxel and oxaliplatin with granulocyte colony-stimulating factor and erythropoietin has a promising therapeutic index in patients with advanced gastroesophageal adenocarcinoma.
机译:进行了一项II期试验,以确定多西他赛加奥沙利铂联合造血生长因子支持在先前未经治疗的晚期胃食管腺癌患者中的疗效和耐受性。该试验纳入了35名患者。治疗包括第1天输注3周的多西他赛80 mg / m和奥沙利铂100 mg / m,皮下给予人类粒细胞集落刺激因子5杯/ kg /天的预防性5天疗程,以及促红细胞生成素(10如果血红蛋白低于12.0 mg / dl,则每周皮下注射3 000 000 IU。确认的总体缓解率为34%,包括两个完全缓解(6%)和10个部分缓解(28%)。 15名患者(43%)病情稳定。中位反应时间为2.5个月(1-3.5),中位进展时间为8.9(4-42.5)个月,中位总生存时间为11.6(2.5-51)个月。尽管世界卫生组织3级或4级中性粒细胞减少症仅发生在6名(17%)患者中,贫血发生在6名(17%)患者中,但血液学毒性很常见。非血液学不良反应通常为轻度至中度。我们的数据表明,多西紫杉醇和奥沙利铂与粒细胞集落刺激因子和促红细胞生成素的组合对晚期胃食管腺癌患者具有有希望的治疗指标。

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