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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Efficacy of FOLFIRI-3 (irinotecan D1,D3 combined with LV5-FU) or other irinotecan-based regimens in oxaliplatin-pretreated metastatic colorectal cancer in the GERCOR OPTIMOX1 study.
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Efficacy of FOLFIRI-3 (irinotecan D1,D3 combined with LV5-FU) or other irinotecan-based regimens in oxaliplatin-pretreated metastatic colorectal cancer in the GERCOR OPTIMOX1 study.

机译:在GERCOR OPTIMOX1研究中,FOLFIRI-3(伊立替康D1,D3与LV5-FU联合使用)或其他基于伊立替康的治疗方案在奥沙利铂预处理的转移性结直肠癌中的疗效。

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摘要

BACKGROUND: Second-line irinotecan-based chemotherapy is commonly used in metastatic colorectal cancers after first-line oxaliplatin-based chemotherapy. No standard schedule of irinotecan has been established in this situation. PATIENTS AND METHODS: Metastatic colorectal cancer patients included in the OPTIMOX1 phase III study received first-line oxaliplatin-based chemotherapy (FOLFOX). No second line was defined in the protocol, but data concerning second line were prospectively registered. Inclusion criterion was patients receiving an irinotecan-based second-line chemotherapy. Second-line progression-free survival (PFS) and tumor response were evaluated according to type of irinotecan-based regimen administered. RESULTS: A total of 342 patients received irinotecan-based chemotherapy as second-line chemotherapy: FOLFIRI-3 [n = 109, irinotecan 100 mg/m(2) days 1 and 3 combined with leucovorin (LV) 400 mg/m(2) day 1 and 46-h continuous 5-fluorouracil (5-FU) 2000 mg/m(2)], FOLFIRI-1 (n = 112, irinotecan 180 mg/m(2) day 1 combined with LV 400 mg/m(2) day 1, 5-FU bolus 400 mg/m(2) and 46-h continuous 5-FU 2400 mg/m(2)) and other various irinotecan-based regimens (n = 121). Median second-line PFS was 3.0 months (FOLFIRI-3: 3.7 months; FOLFIRI-1: 3.0 months; other regimens: 2.3 months). In multivariate analysis, FOLFIRI-3 regimen (relative risk 0.43, 95% confidence interval 0.28-0.68, P = 0.0003) and lactate deshydrogenase level at inclusion (P = 0.0006) in OPTIMOX1 were associated with a longer second-line PFS. CONCLUSION: In unselected patients pretreated with oxaliplatin, PFS in second line appeared to be improved by FOLFIRI-3 regimen.
机译:背景:基于二线伊立替康的化学疗法通常在基于一线奥沙利铂的化学疗法之后用于转移性结直肠癌。在这种情况下,尚未建立伊立替康的标准时间表。患者和方法:OPTIMOX1 III期研究中包括的转移性结直肠癌患者接受了以奥沙利铂为基础的一线化疗(FOLFOX)。协议中未定义第二行,但是有关第二行的数据已预先注册。纳入标准为接受基于伊立替康的二线化疗的患者。根据所用伊立替康治疗方案的类型评估了二线无进展生存期(PFS)和肿瘤反应。结果:共有342例患者接受了基于伊立替康的二线化疗:FOLFIRI-3 [n = 109,伊立替康100 mg / m(2)第1和3天联合亚叶酸(LV)400 mg / m(2 )第1天和46小时连续5-氟尿嘧啶(5-FU)2000 mg / m(2)],FOLFIRI-1(n = 112,伊立替康180 mg / m(2)第1天联合LV 400 mg / m (2)第1天的5-FU推注400 mg / m(2)和46小时的连续5-FU 2400 mg / m(2))和其他各种基于伊立替康的治疗方案(n = 121)。二线PFS中位数为3.0个月(FOLFIRI-3:3.7个月; FOLFIRI-1:3.0个月;其他方案:2.3个月)。在多变量分析中,OPTIMOX1的FOLFIRI-3方案(相对风险0.43,95%置信区间0.28-0.68,P = 0.0003)和乳酸脱氢酶水平(P = 0.0006)与较长的二线PFS相关。结论:未选择的患者接受奥沙利铂预处理后,FOLFIRI-3方案似乎可改善二线患者的PFS。

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