Department of Medicine, Division of Hematology/ Oncology, Geffen School of Medicine at UCLA, Los Angeles, CA.
Massachusetts General Hospital Cancer Center and Harvard Medical School, Boston, MA.
Hepatology. 2018 Jan;67(1):422-435. doi: 10.1002/hep.29486.
Hepatocellular carcinoma (HCC) is a complex disease most commonly arising in the background of chronic liver disease. In the past two decades, there has been a significant increase in our understanding of both the clinical and molecular heterogeneity of HCC. There has been a robust increase in clinical trial activity in patients with poor prognostic factors, such as macrovascular invasion and extrahepatic spread (EHS). We aimed to synthesize the evidence for the treatment of patients with advanced HCC based on these baseline characteristics, including patients with both Child-Pugh (CP) scores of A and B. A comprehensive search of several databases from each database inception to February 15, 2016 any language was conducted. We included 14 studies (three randomized controlled studies [RCTs] and 11 observational studies). We included studies that compared sorafenib, transarterial bland embolization/transarterial chemoembolization, yttrium-90/radiation therapy, ablation (or combination), and no therapy. Two RCTs comparing sorafenib to best supportive care demonstrated a consistent improvement in overall survival (OS) for patients with advanced HCC and metastatic vascular invasion (MVI) and/or EHS and CP A liver disease (hazard ratio, 0.66 [95% confidence interval, 0.51-0.87]; I = 0%). Several observational studies evaluated locoregional therapies alone or in combination with other treatments and were limited by very-low-quality of evidence. This was true for both patients with EHS and MVI.
In patients with advanced HCC and CP A liver function, sorafenib is the only treatment that has been shown to improve OS in randomized studies. High-quality data supporting the use of other treatment modalities in this setting, or in the setting of patients with less compensated (CP B) liver disease, are lacking. (Hepatology 2018;67:422-435).
肝细胞癌(HCC)是一种复杂的疾病,最常发生在慢性肝病的背景下。在过去的二十年中,我们对 HCC 的临床和分子异质性有了更深入的了解。对于预后不良因素(如大血管侵犯和肝外扩散(EHS))的患者,临床试验活动显著增加。我们旨在根据这些基线特征(包括 CP 评分 A 和 B 的患者)综合治疗晚期 HCC 患者的证据,包括 CP 评分 A 和 B 的患者。从每个数据库的创建到 2016 年 2 月 15 日,对多个数据库进行了全面搜索,语言不限。我们纳入了 14 项研究(3 项随机对照试验[RCT]和 11 项观察性研究)。我们纳入了比较索拉非尼、经动脉 bland 栓塞/经动脉化疗栓塞、钇-90/放射治疗、消融(或联合)和无治疗的研究。两项比较索拉非尼与最佳支持治疗的 RCT 表明,对于有晚期 HCC 和转移性血管侵犯(MVI)和/或 EHS 和 CP A 肝脏疾病的患者,总体生存(OS)有一致的改善(风险比,0.66[95%置信区间,0.51-0.87];I=0%)。几项观察性研究评估了单独或联合其他治疗的局部区域治疗,但证据质量非常低。对于有 EHS 和 MVI 的患者都是如此。
在 CP A 肝功能的晚期 HCC 患者中,索拉非尼是唯一在随机研究中显示可改善 OS 的治疗方法。在这种情况下,或在肝功能代偿较差(CP B)的患者中,缺乏支持使用其他治疗方法的数据。(Hepatology 2018;67:422-435)。