Department of Transplantation and Hepatobiliary Surgery, Lahey Clinic Medical Center, 41 Mall Road, 4 West, Burlington, MA 01805, USA.
Liver Transpl. 2010 Mar;16(3):262-78. doi: 10.1002/lt.21999.
A national conference was held to better characterize the long-term outcomes of liver transplantation (LT) for patients with hepatocellular carcinoma (HCC) and to assess whether it is justified to continue the policy of assigning increased priority for candidates with early-stage HCC on the transplant waiting list in the United States. The objectives of the conference were to address specific HCC issues as they relate to liver allocation, develop a standardized pathology report form for the assessment of the explanted liver, develop more specific imaging criteria for HCC designed to qualify LT candidates for automatic Model for End-Stage Liver Disease (MELD) exception points without the need for biopsy, and develop a standardized pretransplant imaging report form for the assessment of patients with liver lesions. At the completion of the meeting, there was agreement that the allocation policy should result in similar risks of removal from the waiting list and similar transplant rates for HCC and non-HCC candidates. In addition, the allocation policy should select HCC candidates so that there are similar posttransplant outcomes for HCC and non-HCC recipients. There was a general consensus for the development of a calculated continuous HCC priority score for ranking HCC candidates on the list that would incorporate the calculated MELD score, alpha-fetoprotein, tumor size, and rate of tumor growth. Only candidates with at least stage T2 tumors would receive additional HCC priority points.
召开了一次全国会议,以更好地描述肝癌 (HCC) 患者肝移植 (LT) 的长期结果,并评估在美国是否有理由继续为移植等候名单上早期 HCC 患者增加优先权的政策。会议的目的是解决与肝脏分配有关的特定 HCC 问题,为评估供体肝脏制定标准化的病理报告表,为 HCC 设计更具体的影像学标准,以便在无需活检的情况下使 LT 候选人有资格获得自动终末期肝病模型 (MELD) 例外分数,并为评估有肝脏病变的患者制定标准化的移植前影像学报告表。会议结束时,与会者一致认为,分配政策应导致 HCC 和非 HCC 候选者从等候名单中除名的风险和移植率相似。此外,分配政策应选择 HCC 候选者,以使 HCC 和非 HCC 受者的移植后结果相似。人们普遍同意为 HCC 候选者在名单上的排名制定一个计算连续 HCC 优先分数,该分数将纳入计算的 MELD 分数、甲胎蛋白、肿瘤大小和肿瘤生长速度。只有至少为 T2 期肿瘤的候选者才会获得额外的 HCC 优先分数。