Department of Medical Oncology 1 Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Cancer. 2011 Jan 1;117(1):125-33. doi: 10.1002/cncr.25578. Epub 2010 Aug 31.
Over the years, doxorubicin and gemcitabine have been among the most widely used drugs for hepatocellular carcinoma (HCC), with relative efficacy. The authors report the results of a phase 2 study of the combination of gemcitabine plus pegylated liposomal doxorubicin.
Patients with advanced HCC received combination chemotherapy with gemcitabine 1000 mg/m² on Days 1 and 8, followed by pegylated liposomal doxorubicin 30 mg/m² on Day 1. Treatment was repeated every 4 weeks to a maximum of 8 cycles. Primary endpoint was overall response rate, and secondary endpoints were time to disease progression (TTP), overall survival (OS), and toxicity.
Forty-one patients were enrolled and were evaluable for response, toxicity, and survival. A total of 194 cycles of treatment were administered. Three (7%) patients had a complete response, and 1 of these patients underwent liver transplantation. Seven (17%) patients had a partial response and, among these patients, 1 patient underwent surgical resection. Among the 31 patients who had initial alpha-fetoprotein levels >400 ng/mL, 20 (64.5%) had a >20% decrease after 2 cycles of treatment. The median TTP and OS were 5.8 and 22.5 months, respectively. Hematologic toxicity was the most common side effect, including neutropenia (17%) and anemia (7%).
The combination of gemcitabine plus pegylated liposomal doxorubicin was active and safe in advanced HCC. Moreover, this treatment induced some complete responses and converted some untreatable HCCs into lesions eligible for resection or transplantation.
多年来,阿霉素和吉西他滨一直是肝癌(HCC)最广泛使用的药物之一,具有相对疗效。作者报告了吉西他滨联合聚乙二醇脂质体阿霉素联合治疗的 2 期研究结果。
晚期 HCC 患者接受吉西他滨 1000mg/m²,第 1 天和第 8 天,随后第 1 天给予聚乙二醇脂质体阿霉素 30mg/m²。每 4 周重复治疗,最多 8 个周期。主要终点是总缓解率,次要终点是疾病进展时间(TTP)、总生存期(OS)和毒性。
41 例患者入组并可评估反应、毒性和生存情况。共给予 194 个周期的治疗。3 例(7%)患者完全缓解,其中 1 例患者接受了肝移植。7 例(17%)患者部分缓解,其中 1 例患者接受了手术切除。在初始 AFP 水平>400ng/mL 的 31 例患者中,20 例(64.5%)在 2 个周期治疗后 AFP 下降>20%。中位 TTP 和 OS 分别为 5.8 个月和 22.5 个月。血液学毒性是最常见的副作用,包括中性粒细胞减少症(17%)和贫血(7%)。
吉西他滨联合聚乙二醇脂质体阿霉素在晚期 HCC 中具有活性和安全性。此外,这种治疗方法诱导了一些完全缓解,并将一些无法治疗的 HCC 转化为可切除或移植的病变。