The 2024 ILTS-ILCA consensus recommendations for liver transplantation for HCC and intrahepatic cholangiocarcinoma

医学 肝移植 肝内胆管癌 肝细胞癌 移植 协商一致会议 人口 肝癌 重症监护医学 内科学 普通外科 肿瘤科 环境卫生
作者
Sudha Kodali,Laura Kulik,Antonio D’Allessio,Eléonora De Martin,Abdul Hakeem,Monika Lewińska,Stacie Lindsey,Ken Liu,Zorana Maravic,Madhukar S. Patel,David J. Pinato,Ashwin Rammohan,Nicole E. Rich,Marco Sanduzzi Zamparelli,David W. Victor,Carmen Vinaxia,Elizabeth W. Brombosz,Augusto Villanueva,Tim Meyer,Nazia Selzner
出处
期刊:Liver Transplantation [Lippincott Williams & Wilkins]
卷期号:31 (6): 815-831 被引量:7
标识
DOI:10.1097/lvt.0000000000000589
摘要

Liver transplantation (LT) provides the best long-term survival outcomes for patients with liver cancer. As a result, the field of transplant oncology has grown greatly over the past few decades, and many centers have expanded their criteria to allow increased access to LT for liver malignancies. Center-level guidelines and practices in transplant oncology significantly vary across the world, leading to debate regarding the best course of treatment for this patient population. An international consensus conference was convened by the International Liver Transplantation Society and the International Liver Cancer Association on February 1-2, 2024, in Valencia, Spain to establish a more universal consensus regarding LT for oncologic indications. The conference followed the Delphi process, followed by an external expert review. Consensus statements were accepted regarding patient assessment and waitlisting criteria, pretransplant treatment (including immunotherapy) and downstaging, living donor LT, post-LT patient management, and patient- and caregiver-related outcomes. The multidisciplinary participants in the consensus conference provided up-to-date recommendations regarding the selection and management of patients with liver cancer being considered for LT. Although participants deferred to center protocols in many cases, there was great interest in safely expanding access to LT for patients with larger tumor burden and biologically amenable lesions.
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