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分子富集在肝细胞癌未来治疗中的作用。

The role of molecular enrichment on future therapies in hepatocellular carcinoma.

机构信息

Unité Mixte de Recherche 1162, Génomique fonctionnelle des tumeurs solides, Institut National de la Santé et de la Recherche Médicale, Paris, France; Liver Unit, Hôpital Jean Verdier, Hôpitaux Universitaires Paris-Seine-Saint-Denis, Assistance-Publique Hôpitaux de Paris, Bondy, France; Unité de Formation et de Recherche Santé Médecine et Biologie Humaine, Université Paris 13, Communauté d'Universités et Etablissements Sorbonne Paris Cité, Paris, France.

Department of Medicine I, Johannes Gutenberg University, Mainz, Germany.

出版信息

J Hepatol. 2018 Jul;69(1):237-247. doi: 10.1016/j.jhep.2018.02.016. Epub 2018 Mar 2.

Abstract

Hepatocellular carcinomas (HCCs) are characterised by considerable phenotypic and molecular heterogeneity. Treating HCC and designing clinical trials are particularly challenging because co-existing liver disease, present in most patients, limits aggressive therapeutic options. Positive results in recent phase III clinical trials have confirmed the high value of anti-angiogenic therapies for HCC in both first (sorafenib and lenvatinib) and second line (regorafenib and cabozantinib) treatment modalities. However, failure of several large randomised controlled clinical trials over the last 10 years underlines the necessity for innovative treatment strategies and implementation of translational findings to overcome the unmet clinical need. Furthermore, the promising results from novel immunotherapies are likely to complement the landscape of active compounds for HCC and will require a completely different approach to patients, as well as the development of prognostic/predictive biomarkers. Given our increasing understanding of the most abundant molecular alterations in HCC, effective enrichment of patients based on clinical and molecular biomarkers, as well as adaptive clinical trials, are now feasible and should be implemented. Herein, we aim to review important aspects of precision medicine approaches in HCC that might contribute to improving the molecular subclassification of patients in a clinical trial setting and pave the way for novel therapeutic strategies.

摘要

肝细胞癌(HCC)具有显著的表型和分子异质性。治疗 HCC 和设计临床试验特别具有挑战性,因为共存的肝病在大多数患者中存在,限制了激进的治疗选择。最近三期临床试验的阳性结果证实了抗血管生成疗法在 HCC 一线(索拉非尼和仑伐替尼)和二线(regorafenib 和 cabozantinib)治疗方案中的高价值。然而,过去 10 年中的几项大型随机对照临床试验的失败突显了需要创新的治疗策略和转化研究结果的实施,以克服未满足的临床需求。此外,新型免疫疗法的有前途的结果可能会补充 HCC 有效化合物的前景,并将需要对患者采取完全不同的方法,以及开发预后/预测生物标志物。鉴于我们对 HCC 中最丰富的分子改变的认识不断增加,基于临床和分子生物标志物的有效患者富集以及适应性临床试验现在是可行的,应该实施。在此,我们旨在回顾 HCC 精准医学方法的重要方面,这些方面可能有助于改善临床试验中患者的分子分类,并为新的治疗策略铺平道路。

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