Department of Gastroenterology and Hepatology, Kinki University School of Medicine, Osaka, Japan.
Dig Dis. 2011;29(3):321-5. doi: 10.1159/000327570. Epub 2011 Aug 9.
The purpose of this study was to evaluate the role of des-γ-carboxyprothrombin (DCP) as a marker for the efficacy of sorafenib therapy for hepatocellular carcinoma (HCC).
Patients with advanced HCC treated with sorafenib were retrospectively evaluated, focusing on DCP levels and clinical characteristics.
50 patients with advanced HCC were treated with sorafenib alone. In 25 of these patients, the serum levels of DCP were evaluated twice (pretreatment and within 2 weeks after starting therapy). The time to progression was significantly longer in patients in whom the DCP level at 2 weeks after starting sorafenib was ≥2-fold higher than the pretreatment levels, as compared with patients without an increase in DCP (p = 0.0296).
The serum level of DCP is a surrogate marker for tissue hypoxia and can be a predictive marker to assess the tumor response to sorafenib therapy.
本研究旨在评估去γ-羧基凝血酶原(DCP)作为索拉非尼治疗肝细胞癌(HCC)疗效标志物的作用。
回顾性评估了接受索拉非尼治疗的晚期 HCC 患者,重点关注 DCP 水平和临床特征。
50 例晚期 HCC 患者单独接受索拉非尼治疗。其中 25 例患者在治疗前和开始治疗后 2 周内评估了两次 DCP 血清水平。与 DCP 水平未升高的患者相比,在开始索拉非尼治疗后 2 周 DCP 水平是治疗前水平的 2 倍以上的患者,其疾病进展时间明显更长(p=0.0296)。
DCP 的血清水平是组织缺氧的替代标志物,可作为预测标志物,用于评估索拉非尼治疗的肿瘤反应。