Pozzo C, Basso M, Cassano A, Quirino M, Schinzari G, Trigila N, Vellone M, Giuliante F, Nuzzo G, Barone C
Unit of Medical Oncology, Department of Internal Medicine, Catholic University of Sacred Heart, Rome, Italy.
Ann Oncol. 2004 Jun;15(6):933-9. doi: 10.1093/annonc/mdh217.
The aim of this study was to observe the effects of neoadjuvant therapy with irinotecan and 5-fluorouracil (5-FU)/folinic acid (FA) on the resection rate and survival of colorectal cancer patients with initially unresectable hepatic metastases.
Forty patients received neoadjuvant chemotherapy comprising irinotecan 180 mg/m(2) administered intravenously (i.v.) on day 1, FA 200 mg/m(2) i.v. on days 1 and 2, 5-FU 400 mg/m(2) i.v. bolus on days 1 and 2, and 5-FU 1200 mg/m(2) as a continuous 48-h i.v. infusion on day 1. The treatment was repeated every 2 weeks and response was assessed every 12 weeks (six cycles).
The objective response rate to chemotherapy was 47.5% (n = 19), with two complete responses and disease stabilization in 11 (27.5.%) patients. Responses were unconfirmed for 11 patients undergoing surgery within 2 weeks. Treatment was well tolerated and adverse events were typical of the chemotherapy agents used. Twenty-seven (67.5%) patients reported hematological toxicity (35.0% grade 3/4) and 14 (35.0%) reported gastrointestinal toxicity (12.5% grade 3/4). Thirteen patients (32.5%) underwent potentially curative liver resection following chemotherapy. Chemotherapy was particularly effective in patients with large metastases on entry to the study. The median time to progression is 14.3 months and, at a median follow-up of 19 months, all patients are alive.
Neoadjuvant therapy with irinotecan combined with 5-FU/FA enabled a significant proportion of patients with initially unresectable liver metastases to undergo surgical resection. The effects of treatment on survival have yet to be determined.
本研究旨在观察伊立替康联合5-氟尿嘧啶(5-FU)/亚叶酸(FA)新辅助治疗对初始不可切除肝转移结直肠癌患者切除率及生存率的影响。
40例患者接受新辅助化疗,方案为第1天静脉注射(i.v.)伊立替康180mg/m²,第1天和第2天静脉注射FA 200mg/m²,第1天和第2天静脉推注5-FU 400mg/m²,第1天持续48小时静脉滴注5-FU 1200mg/m²。每2周重复治疗,每12周(6个周期)评估疗效。
化疗的客观缓解率为47.5%(n = 19),2例完全缓解,11例(27.5%)病情稳定。11例在2周内接受手术的患者的缓解情况未得到确认。治疗耐受性良好,不良事件为所用化疗药物的典型不良反应。27例(67.5%)患者出现血液学毒性(35.0%为3/4级),14例(35.0%)出现胃肠道毒性(12.5%为3/4级)。13例患者(32.5%)在化疗后接受了可能治愈性的肝切除术。化疗对研究入组时存在大转移灶的患者特别有效。中位进展时间为14.3个月,中位随访19个月时,所有患者均存活。
伊立替康联合5-FU/FA新辅助治疗使相当比例的初始不可切除肝转移患者能够接受手术切除。治疗对生存率的影响尚未确定。