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对于经治的转移性结直肠癌,在每两个月一次的大剂量亚叶酸钙以及推注和持续输注5-氟尿嘧啶(FOLFIRI方案)基础上加用CPT-11(伊立替康)。GERCOR研究。

CPT-11 (irinotecan) addition to bimonthly, high-dose leucovorin and bolus and continuous-infusion 5-fluorouracil (FOLFIRI) for pretreated metastatic colorectal cancer. GERCOR.

作者信息

André T, Louvet C, Maindrault-Goebel F, Couteau C, Mabro M, Lotz J P, Gilles-Amar V, Krulik M, Carola E, Izrael V, de Gramont A

机构信息

Service d'Oncologie Médicale, Hôpital Tenon, Paris, France.

出版信息

Eur J Cancer. 1999 Sep;35(9):1343-7. doi: 10.1016/s0959-8049(99)00150-1.

Abstract

CPT-11 (irinotecan) has shown activity in patients with advanced colorectal cancer resistant to leucovorin (LV) and 5-fluorouracil (5-FU). In this study, the simplified bimonthly LV-5-FU regimen was combined with CPT-11 (FOLFIRI) as third-line therapy for patients with advanced colorectal cancer. Continuous infusion of 5-FU was administered with disposable pumps as outpatient therapy. FOLFIRI consisted of CPT-11 180 mg/m2 as a 90-min infusion day 1; LV 400 mg/m2 as a 2-h infusion during CPT-11, immediately followed by 5-FU bolus 400 mg/m2 and 46-h continuous infusion of 2.4-3 g/m2 every 2 weeks. Among the 33 patients treated, 2 had partial responses for an overall response rate of 6%; 20 patients were stabilised (61%) and 11 had disease progression (33%). From the start of FOLFIRI, median progression-free survival was 18 weeks and median survival was 43 weeks. For the 242 cycles analysed, NCI-CTC toxicities grade 3-4 per patient were nausea 15%, diarrhoea 12% and neutropenia 15%. Overall, 10 patients (30%) experienced grade 3-4 toxicity. 7 patients (21%) had grade 2 alopecia. FOLFIRI generated activity and acceptable toxicity, in heavily pretreated patients, with limited diarrhoea, mostly asymptomatic neutropenia and manageable nausea and relatively uncommon alopecia. This regimen is suitable for studies in chemotherapy-naïve patients.

摘要

CPT - 11(伊立替康)已在对亚叶酸钙(LV)和5 - 氟尿嘧啶(5 - FU)耐药的晚期结直肠癌患者中显示出活性。在本研究中,简化的每两个月一次的LV - 5 - FU方案与CPT - 11(FOLFIRI)联合,作为晚期结直肠癌患者的三线治疗。5 - FU持续静脉滴注通过一次性泵作为门诊治疗给药。FOLFIRI方案包括第1天静脉滴注180 mg/m²的CPT - 11,持续90分钟;在CPT - 11静脉滴注期间静脉滴注2小时400 mg/m²的LV,随后立即静脉推注400 mg/m²的5 - FU,并每2周持续静脉滴注2.4 - 3 g/m²,持续46小时。在接受治疗的33例患者中,2例部分缓解,总缓解率为6%;20例病情稳定(61%),11例疾病进展(33%)。从开始使用FOLFIRI起,无进展生存期的中位数为18周,总生存期的中位数为43周。在分析的242个周期中,每位患者的美国国立癌症研究所常见毒性标准(NCI - CTC)3 - 4级毒性为恶心15%、腹泻12%和中性粒细胞减少15%。总体而言,10例患者(30%)出现3 - 4级毒性。7例患者(21%)有2级脱发。FOLFIRI在预处理严重的患者中产生了活性且毒性可接受,腹泻有限,大多数为无症状性中性粒细胞减少,恶心易于控制,脱发相对不常见。该方案适用于未接受过化疗患者的研究。

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