首页> 外文期刊>Clinical oncology >Weekly fluorouracil at 425 mg/m(2) plus low-dose folinic acid for 24 weeks as adjuvant treatment for colorectal cancer: assessment of toxicity and delivery.
【24h】

Weekly fluorouracil at 425 mg/m(2) plus low-dose folinic acid for 24 weeks as adjuvant treatment for colorectal cancer: assessment of toxicity and delivery.

机译:每周425 mg / m(2)氟尿嘧啶加小剂量亚叶酸治疗大肠癌24周:毒性和分娩评估。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

AIMS: To assess the toxicity and dose delivery of weekly bolus 5-fluorouracil (5-FU) at 425 mg/m(2) plus low-dose folinic acid (FA) for 24 weeks as adjuvant treatment for colorectal cancer. MATERIALS AND METHODS: Data were collected on toxicity and dose reductions, stoppages, delays and intensity from 100 consecutive patients receiving this adjuvant regimen after curative surgery. RESULTS: There were 53 men and 47 women (median age: 64 and 65 years, respectively); 77 patients with colon cancer and 23 with cancer of the rectum; 34 patients with Dukes' stage B and 66 with Dukes' stage C. Thirty-seven patients experienced at least one grade 3 or 4 toxicity, mainly diarrhoea (20 patients) or fatigue (14 patients). Only one grade 4 toxicity was noted (diarrhoea). In multivariate analysis, increased grade 3 and 4 toxicity was significantly associated with female gender (P = 0.001) and age >65 years (P = 0.046). Forty patients completed the 24 cycles without dose reduction or delay. Forty-one patients required at least one dose reduction. The median 'conventional' dose intensity (DI), calculated from the first cycle to the last, was 408 mg/m(2)/week (96%). The median DI over 24 weeks was 387 mg/m(2)/week (91%). A higher median 24-week DI was delivered to men (407 mg/m(2)/week, 96%) than women (361 mg/m(2)/ week, 85%; P = 0.009). Women older than 65 years showed a significantly reduced median DI over 24 weeks (347 mg/ m(2)/week, 82%) compared with men aged 65 years or younger (407 mg/m(2)/week, 96%; P = 0.049) and men older than 65 years (425 mg/m(2)/week, 100%; P = 0.001), although the difference against women aged 65 years or younger (377 mg/ m(2)/week, 89%) was not statistically significant (P = 0.09). CONCLUSION: This regimen has shown what might be considered high rates of grade 3 and 4 toxicity for an adjuvant treatment, although the delivered DI was acceptable. Caution is urged in the treatment of elderly female patients who have statistically higher rates of grade 3 and 4 toxicity and lower DI.
机译:目的:评估每周一次推注5-氟尿嘧啶(5-FU)425 mg / m(2)加低剂量亚叶酸(FA)的毒性和剂量,持续24周,作为大肠癌的辅助治疗方法。材料与方法:收集了100例接受根治性手术后接受辅助治疗的患者的毒性和剂量减少,停药,延迟和强度的数据。结果:男性53例,女性47例(中位年龄分别为64岁和65岁)。 77例结肠癌患者和23例直肠癌患者;杜克B期患者34例,杜克C期患者66例。三十七名患者至少有一种3级或4级毒性,主要是腹泻(20例)或疲劳(14例)。仅注意到一种4级毒性(腹泻)。在多变量分析中,3级和4级毒性增加与女性性别(P = 0.001)和年龄> 65岁(P = 0.046)显着相关。 40名患者完成了24个周期而没有减少剂量或延迟剂量。 41位患者需要减少至少一种剂量。从第一个周期到最后一个周期计算得出的“常规”剂量强度(DI)中值为408 mg / m(2)/周(96%)。在24周内,DI的中位数为387 mg / m(2)/周(91%)。与女性(361 mg / m(2)/周,85%; P = 0.009)相比,男性(407 mg / m(2)/周,中位24周DI的中位数更高)。 65岁以上的女性在24周内的中值DI显着降低(347 mg / m(2)/周,82%),而65岁或更年轻的男性(407 mg / m(2)/周,96%); P = 0.049)和65岁以上的男性(425 mg / m(2)/周,100%; P = 0.001),尽管与65岁以下的女性(377 mg / m(2)/周, 89%)差异无统计学意义(P = 0.09)。结论:该方案显示了辅助治疗的高3级和4级毒性反应,尽管所提供的DI可以接受。在治疗老年女性患者时,应谨慎对待,其统计学上具有较高的3级和4级毒性发生率,且DI较低。

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