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Sorafenib for the treatment of advanced hepatocellular carcinoma with extrahepatic metastasis: a prospective multicenter cohort study

机译:索拉非尼治疗晚期肝细胞癌伴肝外转移的前瞻性多中心队列研究

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摘要

Sorafenib, an oral multikinase inhibitor, is approved for advanced hepatocellular carcinoma (HCC) treatment. However, its therapeutic effect in advanced HCC patients with extrahepatic metastasis remains uncertain. This study aimed to prospectively assess the efficacy, safety, and survival risk factors and evaluate the prognostic impact of sorafenib treatment in advanced HCC patients with or without extrahepatic metastasis. Between May 2009 and March 2014, 312 consecutive advanced HCC patients who received sorafenib were enrolled in this study. We evaluated their characteristics and compared the clinical outcomes of those with and without extrahepatic metastasis. Of the enrolled patients, 245 (81%) received sorafenib treatment for more than 1 month, with a median duration of 3.6 months. Eighteen patients demonstrated partial response to sorafenib therapy, 127 had stable disease, and 134 had progressive disease at the first radiologic assessment. The median survival time (MST) and progression‐free survival (PFS) were 10.3 and 3.6 months, respectively. Multivariate analysis identified gender, Child‐Pugh class, baseline serum des‐gamma‐carboxy prothrombin level, and treatment duration as independent risk factors for survival. Extrahepatic metastasis was detected in 178 patients. However, the MST, PFS, and therapeutic effect were comparable between patients with and without extrahepatic metastasis. The independent risk factors for decreased overall survival in patients with extrahepatic metastasis were similar to those affecting all patients. Our results indicated that sorafenib could be administered for hepatic reserve and as long‐term treatment for advanced HCC patients regardless of their extrahepatic metastasis status.
机译:口服多激酶抑制剂索拉非尼被批准用于晚期肝细胞癌(HCC)治疗。然而,其在晚期肝癌肝外转移患者中的治疗效果仍不确定。这项研究旨在前瞻性评估疗效,安全性和生存风险因素,并评估索拉非尼治疗对有或无肝外转移的晚期HCC患者的预后影响。在2009年5月至2014年3月之间,本研究共纳入312位接受索拉非尼治疗的晚期HCC患者。我们评估了它们的特征,并比较了有无肝外转移的患者的临床结局。在入组患者中,有245名(81%)接受索拉非尼治疗超过1个月,中位时间为3.6个月。在首次放射学评估中,有18名患者对索拉非尼治疗表现出部分反应,其中127例疾病稳定,而134例疾病进行性。中位生存时间(MST)和无进展生存期(PFS)分别为10.3和3.6个月。多变量分析确定了性别,Child-Pugh类,基线血清脱γ-羧基凝血酶原水平和治疗持续时间是生存的独立危险因素。 178例患者检测到肝外转移。然而,在有无肝外转移的患者中,MST,PFS和治疗效果相当。肝外转移患者降低总生存的独立危险因素与影响所有患者的相似。我们的结果表明,索拉非尼可用于肝储备和作为晚期HCC患者的长期治疗,无论其肝外转移状况如何。

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