J Hepatol. 2023 Jul;79(1):181-208. doi: 10.1016/j.jhep.2023.03.010. Epub 2023 Apr 20.
Intrahepatic cholangiocarcinoma (iCCA) develops inside the liver, between bile ductules and the second-order bile ducts. It is the second most frequent primary liver cancer after hepatocellular carcinoma, and its global incidence is increasing. It is associated with an alarming mortality rate owing to its silent presentation (often leading to late diagnosis), highly aggressive nature and resistance to treatment. Early diagnosis, molecular characterisation, accurate staging and personalised multidisciplinary treatments represent current challenges for researchers and physicians. Unfortunately, these challenges are beset by the high heterogeneity of iCCA at the clinical, genomic, epigenetic and molecular levels, very often precluding successful management. Nonetheless, in the last few years, progress has been made in molecular characterisation, surgical management, and targeted therapy. Recent advances together with the awareness that iCCA represents a distinct entity amongst the CCA family, led the ILCA and EASL governing boards to commission international experts to draft dedicated evidence-based guidelines for physicians involved in the diagnostic, prognostic, and therapeutic management of iCCA.
肝内胆管癌(iCCA)发生在肝脏内部,在胆管小管和二级胆管之间。它是继肝细胞癌之后第二常见的原发性肝癌,其全球发病率正在上升。由于其隐匿性表现(常导致晚期诊断)、高度侵袭性和对治疗的耐药性,其死亡率令人震惊。早期诊断、分子特征、准确分期和个体化多学科治疗是当前研究人员和医生面临的挑战。不幸的是,这些挑战受到 iCCA 在临床、基因组、表观遗传学和分子水平上高度异质性的困扰,常常使治疗无法成功。尽管如此,在过去几年中,在分子特征、手术管理和靶向治疗方面已经取得了进展。最近的进展以及认识到 iCCA 是 CCA 家族中的一个独特实体,促使 ILCA 和 EASL 理事会委托国际专家为参与 iCCA 诊断、预后和治疗管理的医生制定专门的循证指南。