Division of Gastroenterology and Hepatology, Department of Internal Medicine, Iwate Medical University, Morioka, Iwate, Japan.
Cancer. 2012 Jul 1;118(13):3302-10. doi: 10.1002/cncr.26648. Epub 2011 Nov 9.
The prognosis of advanced hepatocellular carcinoma (HCC) remains poor, particularly among patients with portal vein tumor thrombosis (PVTT). This study evaluated the efficacy of combined 5-fluorouracil and pegylated interferon (PEG-IFN) α-2b in patients with advanced HCC.
Subjects comprised 59 HCC patients with PVTT treated using subcutaneous administration of PEG-IFNα-2b (50-100 μg on day 1 of each week for 4 weeks) and intra-arterial infusion of 5-fluorouracil (250 mg/d for 5 hours on days 1-5 of each week for 4 weeks). One treatment cycle lasted 4 weeks. The current therapy was discontinued in patients with progressive disease (PD). For responses other than PD, treatment was repeated for ≥1 cycle. The primary efficacy endpoint was the objective early response rate. Secondary efficacy endpoints were progression-free survival (PFS) and overall survival.
Objective early response rate was 73.0%. Cumulative PFS rates were 67.4% at 6 months, 30.2% at 12 months, 25.9% at 18 months, and 20.7% at 24 months. Median PFS was 9.7 months. Cumulative survival rates were 82.4% at 6 months, 73.6% at 12 months, 52.8% at 24 months, and 44.0% at 36 months. Median survival time was 29.9 months. All adverse reactions were controllable by temporary suspension of treatment. Serious complications and treatment-related deaths were not observed.
Although a prospective randomized controlled trial using a larger population of patients with advanced HCC is needed to evaluate combination therapy with 5-fluorouracil and PEG-IFNα-2b, this new combination therapy may be useful for patients with advanced HCC.
晚期肝细胞癌(HCC)的预后仍然较差,尤其是伴有门静脉癌栓(PVTT)的患者。本研究评估了氟尿嘧啶联合聚乙二醇干扰素(PEG-IFN)α-2b 治疗晚期 HCC 的疗效。
59 例 HCC 合并 PVTT 患者接受皮下注射 PEG-IFNα-2b(每周 1 天,第 1 天 50-100 μg,连续 4 周)联合肝动脉灌注氟尿嘧啶(每周 1-5 天,每天 250 mg,连续 5 小时,连续 4 周)治疗。1 个治疗周期为 4 周。疾病进展(PD)患者停止当前治疗。对于 PD 以外的反应,重复治疗至少 1 个周期。主要疗效终点为客观早期反应率。次要疗效终点为无进展生存期(PFS)和总生存期。
客观早期反应率为 73.0%。6 个月时累积 PFS 率为 67.4%,12 个月时为 30.2%,18 个月时为 25.9%,24 个月时为 20.7%。中位 PFS 为 9.7 个月。6 个月时累积生存率为 82.4%,12 个月时为 73.6%,24 个月时为 52.8%,36 个月时为 44.0%。中位总生存期为 29.9 个月。所有不良反应均可通过暂时停止治疗控制。未观察到严重并发症和与治疗相关的死亡。
尽管需要一项前瞻性随机对照试验,用更大的晚期 HCC 患者群体评估氟尿嘧啶联合 PEG-IFNα-2b 的联合治疗,但这种新的联合治疗可能对晚期 HCC 患者有用。