首页> 外文期刊>Anti-cancer drugs >Weekly high-dose 5-fluorouracil as 24-h infusion and folinic acid (AIO) plus irinotecan as second- and third-line treatment in patients with colorectal cancer pre-treated with AIO plus oxaliplatin.
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Weekly high-dose 5-fluorouracil as 24-h infusion and folinic acid (AIO) plus irinotecan as second- and third-line treatment in patients with colorectal cancer pre-treated with AIO plus oxaliplatin.

机译:在接受AIO加奥沙利铂预处理的大肠癌患者中,每周高剂量5-氟尿嘧啶24小时输注和亚叶酸(AIO)加伊立替康作为二线和三线治疗。

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Our objective was to evaluate the efficacy and safety of high-dose 5-fluorouracil (5-FU) as a 24-h infusion and folinic acid (FA) (AIO regimen) plus irinotecan (CPT-11) after pre-treatment with AIO plus oxaliplatin (L-OHP) in colorectal carcinoma (CRC). Twenty-six patients with non-resectable distant CRC metastases were analyzed for second- or third-line treatment with AIO plus CPT-11 after pre-treatment with AIO plus L-OHP. On an outpatient basis, the patients received a treatment regimen comprising weekly 80 mg/m2 CPT-11 in the form of a 1-h i.v. infusion and 500 mg/m2 FA as a 1- to 2-h i.v. infusion, followed by 2000 mg/m2 5-FU i.v. administered as a 24-h infusion once weekly. A single treatment cycle comprised six weekly infusions followed by 2 weeks of rest. A total of 26 patients received 344 chemotherapy applications with AIO plus CPT-11. The main symptom of toxicity was diarrhea (NCI-CTC toxicity grade 3+4) occurring in five patients (19%; 95% CI 7-39%). Nausea and vomiting presented in two patients (8%; 95% CI 1-25%). The response rate of 26 patients can be summarized as follows: partial remission: n=7 (27%; 95% CI 12-48%); stable disease: n=9 (35%; 95% CI 17-56%) and progressive disease: n=10 (38%; 95% CI 20-59%). The median progression-free survival (n=26) was 5.8 months (range 3-13), the median survival time counted from the treatment start with the AIO plus CPT-11 regimen was 10 months (range 2-24) and counted from the start of first-line treatment (n=26) was 23 months (range 10-66). We conclude that the AIO regimen plus CPT-11 is practicable in an outpatient setting and well tolerated by the patients. Tumor control was achieved in 62% of the patients. The median survival time was 10 months and the median survival time from the start of first-line treatment (n=26) was 23 months.
机译:我们的目标是评估AIO预处理后大剂量5-氟尿嘧啶(5-FU)作为24小时输注和亚叶酸(FA)(AIO方案)加伊立替康(CPT-11)的疗效和安全性加上奥沙利铂(L-OHP)治疗大肠癌(CRC)。在AIO加L-OHP预处理后,对26例不可切除的远处CRC转移患者进行了AIO加CPT-11的二线或三线治疗。在门诊患者的基础上,患者接受每周1次静脉输注80 mg / m2 CPT-11的治疗方案。静脉输注和每小时1到2小时500 mg / m2 FA。输注,然后静脉输注2000 mg / m2 5-FU。每周一次24小时输注。一个治疗周期包括每周输注6次,然后休息2周。共有26位患者接受了344例AIO加CPT-11化疗。毒性的主要症状是腹泻(NCI-CTC毒性等级3 + 4),发生在五名患者中(19%; 95%CI 7-39%)。两名患者出现恶心和呕吐(8%; 95%CI 1-25%)。 26例患者的缓解率可归纳如下:部分缓解:n = 7(27%; 95%CI 12-48%);稳定疾病:n = 9(35%; 95%CI 17-56%)和进行性疾病:n = 10(38%; 95%CI 20-59%)。中位无进展生存期(n = 26)为5.8个月(范围3-13),从AIO加CPT-11方案开始治疗的中位生存时间为10个月(范围2-24),从一线治疗的开始时间(n = 26)为23个月(范围10-66)。我们得出的结论是,AIO方案加CPT-11在门诊患者中是可行的,并且患者可以很好地耐受。 62%的患者达到了肿瘤控制。中位生存时间为10个月,从一线治疗开始(n = 26)开始的中位生存时间为23个月。

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