Shao Yu-Yun, Shau Wen-Yi, Chan Soa-Yu, Lu Li-Chun, Hsu Chih-Hung, Cheng Ann-Lii
Department of Oncology, National Taiwan University Hospital, New Taipei City, Taiwan, ROC.
Oncology. 2015;88(6):345-52. doi: 10.1159/000369559. Epub 2015 Jan 7.
Hepatocellular carcinoma (HCC) is a heterogeneous disease. We explored whether any specific subgroups of patients may gain more survival benefits from sorafenib as the first-line therapy for advanced HCC.
PubMed and the Cochrane library were searched for phase III clinical trials that compared sorafenib with other treatments as first-line therapy for advanced HCC. We retrieved data from the published articles and then calculated synthesized hazard ratios (HRs) of overall mortality for patients of different subgroups, using patients who received other treatments as the reference.
Four phase III clinical trials comparing sorafenib with other treatments were included in this study. The HRs were not significantly different between patients from various geographic regions (p = 0.183), patients with different Eastern Cooperative Oncology Group performance statuses (p = 0.699), or patients with different tumor involvement (p = 0.221). By contrast, the synthesized HR for hepatitis C virus (HCV)+ patients was 0.65 [95% confidence interval (CI) 0.53-0.80], which was significantly lower than that for HCV- patients (0.87, 95% CI 0.79-0.96, p = 0.013).
As the first-line therapy for advanced HCC, sorafenib might provide more survival benefits to HCV+ patients than to HCV- patients.
肝细胞癌(HCC)是一种异质性疾病。我们探讨了对于晚期HCC患者,是否有特定亚组能从索拉非尼作为一线治疗中获得更多生存益处。
检索PubMed和Cochrane图书馆,查找比较索拉非尼与其他治疗作为晚期HCC一线治疗的III期临床试验。我们从已发表文章中提取数据,然后以接受其他治疗的患者为对照,计算不同亚组患者全因死亡率的综合风险比(HRs)。
本研究纳入了四项比较索拉非尼与其他治疗的III期临床试验。不同地理区域的患者(p = 0.183)、不同东部肿瘤协作组体能状态的患者(p = 0.699)或不同肿瘤累及情况的患者(p = 0.221)之间,HRs无显著差异。相比之下,丙型肝炎病毒(HCV)阳性患者的综合HR为0.65 [95%置信区间(CI)0.53 - 0.80],显著低于HCV阴性患者(0.87,95% CI 0.79 - 0.96,p = 0.013)。
作为晚期HCC的一线治疗,索拉非尼可能为HCV阳性患者提供比HCV阴性患者更多的生存益处。