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肝移植术后奥沙利铂、5-氟尿嘧啶和亚叶酸钙联合辅助化疗治疗肝细胞癌:一项初步的开放标签研究。

Combination adjuvant chemotherapy with oxaliplatin, 5-fluorouracil and leucovorin after liver transplantation for hepatocellular carcinoma: a preliminary open-label study.

机构信息

Institute of Liver Transplantation, General Hospital of Chinese People's Armed Police Force, 69 Yongding Road, Haidian District, Beijing, 100039, China.

出版信息

Invest New Drugs. 2011 Dec;29(6):1360-9. doi: 10.1007/s10637-011-9726-1. Epub 2011 Aug 2.

Abstract

The purpose of this study was to evaluate the efficacy of postoperative adjuvant chemotherapy with FOLFOX regimen on the outcome after LT for HCC patients who did not meet the Milan criteria. Ninety-five consecutive HCC patients with liver cirrhosis undergoing LT were enrolled. Fifty-eight who did not meet the Milan criteria were randomized to open-label treatment with or without adjuvant chemotherapy after LT (n = 29/group). The FOLFOX chemotherapy protocol comprised 3-week cycles of oxaliplatin 100 mg/m(2) on day 1, leucovorin (calcium folinate, CF) 200 mg/m(2) on day 1 followed by 3-day, and 5-fluorouracil (5-FU) 2000 mg/m(2) as a 48-h continuous infusion, for up to six courses in the 1st year after transplantation. Median survival was extended by 4.57 months by combination chemotherapy. The 1- and 3-year survival rates were 89.7% and 79.3% with chemotherapy versus 69.0% and 62.1% without chemotherapy. The cumulative 1-year survival was significantly increased by chemotherapy (log-rank test, P = 0.043). The 6-month tumor-free survival rate was 24.1% higher with chemotherapy than without. The recurrence rate after LT was significantly different between the two groups at 6 months (P = 0.036), but not at 3 years (P = 0.102). The chemotherapy regimen was generally well tolerated. Post-LT adjuvant chemotherapy with oxaliplatin/5-FU/CF could not prevent tumor recurrence post-LT but may contribute to improve the survival of HCC patients who do not meet the Milan criteria. These results should be verified in a larger sample with a longer follow-up period.

摘要

本研究旨在评估术后辅助 FOLFOX 方案化疗对不符合米兰标准的 HCC 患者行肝移植(LT)后的疗效。共纳入 95 例连续行 LT 的 HCC 合并肝硬化患者,其中 58 例不符合米兰标准,随机分为 LT 后行或不行辅助化疗(n = 29/组)。FOLFOX 化疗方案包括:奥沙利铂 100 mg/m²(第 1 天),亚叶酸钙(calcium folinate,CF)200 mg/m²(第 1 天),5-氟尿嘧啶(5-FU)2000 mg/m²(第 1 天),3 天输注,5-FU 持续 48 小时输注,1 年内共 6 个周期。联合化疗使中位生存时间延长 4.57 个月。化疗组的 1 年和 3 年生存率分别为 89.7%和 79.3%,而未化疗组分别为 69.0%和 62.1%。化疗组的 1 年累积生存率显著高于未化疗组(log-rank 检验,P = 0.043)。化疗组的 6 个月无瘤生存率比未化疗组高 24.1%。两组在 LT 后 6 个月的复发率存在显著差异(P = 0.036),但在 3 年后无差异(P = 0.102)。化疗方案总体耐受良好。奥沙利铂/5-FU/CF 术后辅助化疗不能预防 LT 后肿瘤复发,但可能有助于提高不符合米兰标准的 HCC 患者的生存率。这些结果应在更大样本和更长随访期内得到验证。

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