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检查点抑制疗法治疗不可切除的晚期淋巴上皮瘤样肝细胞癌

Checkpoint Inhibition in the Treatment of Unresectable, Advanced Lymphoepithelioma-like Hepatocellular Carcinoma.

作者信息

Hermel David J, Du Emma Z, Lin Ray, Frenette Catherine T, Sigal Darren S

机构信息

Division of Hematology and Oncology, Scripps Clinic and Scripps MD Anderson Cancer Center, La Jolla, CA, USA.

Division of Pathology, Scripps Clinic and Scripps MD Anderson Cancer Center, La Jolla, CA, USA.

出版信息

J Clin Transl Hepatol. 2021 Apr 28;9(2):265-268. doi: 10.14218/JCTH.2020.00094. Epub 2021 Feb 1.

Abstract

Lymphoepithelioma-like hepatocellular carcinoma (LEL-HCC) is a very rare neoplasm, with distinct epidemiologic, morphologic and clinical characteristics. Molecular mechanistic insight into the pathogenesis of this carcinoma suggests a pivotal role for the host immune system in the proliferation and progression of this tumor. However, while detailed genomic profiling of these hepatic tumors have revealed an intra-tumoral inflammatory mutational signature that may predispose to immune checkpoint inhibitor efficacy, no published report has described their use in this tumor type. Unfortunately, with near 100 cases of LEL-HCC reported in the literature to date and the majority of cases confined to localized and resectable disease, current evidence-based practices in the unresectable setting are lacking, with unknown benefit of chemotherapy or immunotherapy. We report on the case of a 68 year-old man with unresectable, advanced LEL-HCC who had evidence of disease stability after starting on the immune checkpoint inhibitor nivolumab. His disease response persisted off therapy for over a year and was potentially augmented by radiotherapy at the site of local progression. For this extremely rare tumor subtype, this case highlights the potential efficacy and safety of immune checkpoint blockade in LEL-HCC and reinforces the need for more robust, large-scale analysis of patients with these rare tumors to better evaluate treatment strategies and outcomes.

摘要

淋巴上皮瘤样肝细胞癌(LEL-HCC)是一种非常罕见的肿瘤,具有独特的流行病学、形态学和临床特征。对该癌症发病机制的分子机制研究表明,宿主免疫系统在这种肿瘤的增殖和进展中起关键作用。然而,尽管对这些肝肿瘤的详细基因组分析揭示了一种可能使免疫检查点抑制剂有效的肿瘤内炎症突变特征,但尚无已发表的报告描述其在这种肿瘤类型中的应用。不幸的是,迄今为止文献中报道了近100例LEL-HCC病例,且大多数病例局限于局部和可切除疾病,在不可切除情况下目前缺乏循证实践,化疗或免疫治疗的益处尚不清楚。我们报告了一例68岁患有不可切除的晚期LEL-HCC的男性病例,该患者在开始使用免疫检查点抑制剂纳武单抗后有疾病稳定的证据。他的疾病反应在停止治疗后持续了一年多,并且在局部进展部位进行放疗后可能得到增强。对于这种极其罕见的肿瘤亚型,该病例突出了免疫检查点阻断在LEL-HCC中的潜在疗效和安全性,并强化了对这些罕见肿瘤患者进行更有力、大规模分析以更好评估治疗策略和结果的必要性。

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