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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Weekly High-dose 5-Fluorouracil as 24-hour Infusion Combined with Sodium Folinic Acid (AIO regimen) Plus Irinotecan in Second-line and Sequential Therapy of Metastatic Colorectal Cancer (CRC)
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Weekly High-dose 5-Fluorouracil as 24-hour Infusion Combined with Sodium Folinic Acid (AIO regimen) Plus Irinotecan in Second-line and Sequential Therapy of Metastatic Colorectal Cancer (CRC)

机译:每周高剂量5-氟尿嘧啶作为24小时输注联合枯草酸钠(AIO方案)加上伊替康在二线和转移结直肠癌(CRC)的顺序治疗

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Background/Aim: The aim of this work was to evaluate the efficacy and safety of second-line treatment with weekly high-dose 5-fluorouracil (5-FU) as a 24-hour infusion (24-h inf.) combined with sodium folinic acid (FA) (AIO-regimen) plus irinotecan (Iri.) after pretreatment with AIO-regimen plus oxaliplatin (L-OHP). Patients and Methods: Patients with non-resectable distant CRC metastases were enrolled in a prospective phase II study for palliative second-line treatment after previous progression of first-line treatment in accordance with the AIO-regimen plus oxaliplatin. On an outpatient basis, the patients received a treatment regimen comprising of weekly 80 mg/m(2) irinotecan in the form of a 1-hour i.v. infusion and 2,000 mg/m(2) 5-FU combined with 500 mg/m(2) sodium folinic acid administered as a 24-h infusion i.v. once weekly. Results: During secondline treatment, a total of 59 patients received 520 chemotherapy applications. As the main higher-grade symptom of toxicity, diarrhea (NCI-CTC-toxicity grade 3) presented in 8 patients (13.6%, 95% CI=5.1-23.7), followed by leukocytopenia (CTC grade 3) in 3 patients (5.1%, 95% CI=0-11.9), followed by thrombocytopenia (CTC grade 3) in 1 patient (1.7%, 95% CI=0-5.1). Fifty-nine patients were evaluable for treatment response. The remission data can be summarized as follows: complete remission (CR); n=0; partial remission (PR); n=6 (10%; 95% CI=3.4-18.6); stable disease (SD); n=31 (53%; 95% CI=39.0-64.4); progressive disease (PD); n=19 (33%; 95% CI=20.3-44.1). The median progression-free survival (PFS) rate (n=59) was 4.2 months (range=3.8-5.8 months). The median survival time counted from the start of second-line treatment (n=59) 14.2 months (range 8.2-17.3 months) and the median survival time counted from the start of first-line therapy (n=59) 25 months (range 19-27 months). Conclusion: Palliative second-line treatment according to the AIO regimen plus irinotecan offers both a favourable toxicity profile and promising efficacy in second-line and palliative sequential therapy.
机译:背景/目标:这项工作的目的是评估每周高剂量5-氟尿嘧啶(5-FU)作为24小时输注(24-HIM。)与钠相结合的二线治疗的疗效和安全性叶酸(FA)(AIO-方案)加上IRINOTECAN(IRI。)在使用AIO-RENIMEN加上oxaliplatin(L-OHP)进行预处理后。患者和方法:在根据AIO-Regimen Plus oxaliplatin的先前进展后,患有不可切除的远程CRC转移患者在先前进展后进行姑息二线治疗的前瞻性二线治疗。在门诊,患者接受了每周80mg / m(2)伊立替康的治疗方案,以1小时I.V。输注和2,000mg / m(2)5-fu合并500mg / m(2)钠叶酸作为24-h输注I.v。每周一次。结果:在第二次治疗过程中,共有59名患者接受了520名化疗应用。作为毒性的主要较高症状,腹泻(NCI-CTC毒性3级)在8名患者(13.6%,95%CI = 5.1-23.7)中,其次是3名患者的白细胞减少症(CTC等级3)(5.1 %,95%CI = 0-11.9),其次是1例(1.7%,95%CI = 0-5.1)中的血小板减少症(CTC级3)。 59名患者对治疗反应进行评估。缓解数据可以概括如下:完全缓解(CR); n = 0;部分缓解(PR); n = 6(10%; 95%CI = 3.4-18.6);稳定的疾病(SD); n = 31(53%; 95%CI = 39.0-64.4);进行性疾病(PD); n = 19(33%; 95%CI = 20.3-44.1)。中位进展生存期(PFS)率(N = 59)为4.2个月(范围= 3.8-5.8个月)。从二线治疗开始(n = 59)14.2个月(范围8.2-17.3个月)和从一线治疗开始(n = 59)25个月(范围)计算的中位存活时间(范围19-27个月)。结论:根据Aio Regimen Plus Irinotecan的姑息性二线治疗在二线和姑息性连续治疗中提供了有利的毒性概况和有希望的疗效。

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