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纤维板层肝细胞癌:挑战中的挑战。

Fibrolamellar carcinoma: Challenging the challenge.

机构信息

Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester, United Kingdom; Division Cancer Sciences, University of Manchester; Manchester, United Kingdom.

Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester, United Kingdom.

出版信息

Eur J Cancer. 2020 Sep;137:144-147. doi: 10.1016/j.ejca.2020.06.035. Epub 2020 Aug 5.

Abstract

Fibrolamellar carcinoma (FLC) is a rare and poorly understood malignancy, which seems to be more prevalent in young patients compared with conventional hepatocellular carcinoma (HCC). Performing prospective clinical trials recruiting patients diagnosed with FLC has proven challenging with scarce data available guiding clinical management. The use of a number of chemotherapy compounds in these patients, including cisplatin, epirubicin, 5-fluorouracil (5-FU) and recombinant interferon α-2B (IFN-α-2B), has been reported in the literature, mainly in the form of case reports. The most promising systemic therapy tested so far is the combination of 5-FU infusion and 3-weekly IFN-α-2B, based on results from a phase II clinical trial. This article provides an overview of our own experience with this treatment schedule for patients with FLC, confirming its activity and treatment-derived benefit in the real world. Current challenges being faced by healthcare professionals treating patients with advanced FLC are discussed, especially the increasingly limited access to IFN-α-2B, which could compromise the access to an active therapy in the coming future, and the difficulties in the development of new treatment options for advanced FLC.

摘要

纤维板层肝细胞癌(FLC)是一种罕见且尚未被充分了解的恶性肿瘤,与传统的肝细胞癌(HCC)相比,其似乎更常见于年轻患者。由于缺乏指导临床管理的可用数据,对确诊为 FLC 的患者进行前瞻性临床试验招募一直具有挑战性。文献中报道了许多在这些患者中使用的化疗药物,包括顺铂、表柔比星、5-氟尿嘧啶(5-FU)和重组干扰素α-2B(IFN-α-2B),主要以病例报告的形式报告。迄今为止,经过测试的最有前途的系统治疗方法是 5-FU 输注联合每周 3 次 IFN-α-2B,这是基于一项 II 期临床试验的结果。本文概述了我们使用这种治疗方案治疗 FLC 患者的经验,证实了它在现实世界中的活性和治疗获益。讨论了目前治疗晚期 FLC 患者的医疗保健专业人员面临的挑战,特别是越来越有限地获得 IFN-α-2B,这可能会在未来限制对有效治疗方法的获得,以及开发晚期 FLC 新治疗方案的困难。

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