Wörns Marcus Alexander, Weinmann Arndt, Pfingst Kerstin, Schulte-Sasse Carla, Messow Claudia-Martina, Schulze-Bergkamen Henning, Teufel Andreas, Schuchmann Marcus, Kanzler Stephan, Düber Christoph, Otto Gerd, Galle Peter Robert
I Department of Internal Medicine, Johannes Gutenberg-University Mainz, Germany.
J Clin Gastroenterol. 2009 May-Jun;43(5):489-95. doi: 10.1097/MCG.0b013e31818ddfc6.
The multikinase inhibitor sorafenib provides survival benefit for patients with advanced hepatocellular carcinoma (HCC) and liver cirrhosis (LCI) Child-Pugh A. We report our experiences with sorafenib in advanced HCC, particularly in patients with LCI Child-Pugh B/C, where only limited data are available in regard to safety and efficacy of sorafenib.
Thirty-four patients with advanced HCC were treated with sorafenib regardless of liver function and prior anticancer therapy. Adverse events (AEs) were graded using Common Toxicity Criteria version 3.0, tumor response was assessed according to Response Evaluation Criteria in Solid Tumors.
Fifteen patients presented without LCI or with LCI Child- Pugh A, 15/4 patients had LCI Child-Pugh B/C. Barcelona Clinic Liver Cancer stage was B/C/D in 4/22/8 patients. During treatment period (median 2.2 mo), therapy was discontinued in 61.8% of patients due to tumor progression (32.3%), death (17.6%), AEs (8.8%), or noncompliance (2.9%). Most common grade 3/4 AEs included liver dysfunction (23.5%), diarrhea (14.7%), increased lipase (8.8%), fatigue (8.8%), and hand-foot skin reaction (5.9%). Worsening liver dysfunction/failure was more frequent (P=0.036) in patients with LCI Child-Pugh B/C compared with patients with maintained liver function (no LCI/LCI Child-Pugh A). Median overall survival was 7.2 months for patients with maintained liver function versus 3.3/3.4 months for patients with LCI Child-Pugh B/C.
These data do not support the use of sorafenib in patients with LCI Child-Pugh C, and patients with LCI Child-Pugh B should be treated with caution until larger trials provide more safety data and a clinically relevant survival benefit under sorafenib therapy.
多激酶抑制剂索拉非尼可使晚期肝细胞癌(HCC)和Child-Pugh A级肝硬化(LCI)患者的生存期延长。我们报告了索拉非尼治疗晚期HCC的经验,尤其是在Child-Pugh B/C级LCI患者中,关于索拉非尼安全性和疗效的可用数据有限。
34例晚期HCC患者接受索拉非尼治疗,无论其肝功能及既往抗癌治疗情况如何。不良事件(AE)按照通用毒性标准3.0版进行分级,肿瘤反应根据实体瘤疗效评价标准进行评估。
15例患者无LCI或为Child-Pugh A级LCI,15/4例患者为Child-Pugh B/C级LCI。巴塞罗那临床肝癌分期为B/C/D期的患者分别有4/22/8例。在治疗期间(中位时间2.2个月),61.8%的患者因肿瘤进展(32.3%)、死亡(17.6%)、AE(8.8%)或不依从(2.9%)而停药。最常见的3/4级AE包括肝功能不全(23.5%)、腹泻(14.7%)、脂肪酶升高(8.8%)、疲劳(8.8%)和手足皮肤反应(5.9%)。与肝功能维持正常(无LCI/Child-Pugh A级LCI)的患者相比,Child-Pugh B/C级LCI患者肝功能恶化/衰竭更为常见(P=0.036)。肝功能维持正常的患者中位总生存期为7.2个月,而Child-Pugh B/C级LCI患者为3.3/3.4个月。
这些数据不支持在Child-Pugh C级LCI患者中使用索拉非尼,对于Child-Pugh B级LCI患者应谨慎治疗,直至有更大规模试验提供更多安全性数据以及索拉非尼治疗下具有临床意义的生存获益。