Suppr超能文献

晚期肝细胞癌的肝移植

Liver transplantation for advanced hepatocellular carcinoma.

作者信息

Lee Hae Won, Suh Kyung-Suk

机构信息

Department of Surgery, Seoul National University College of Medicine, Seoul, Korea.

Department of Surgery, Seoul National University Boramae Medical Center, Seoul, Korea.

出版信息

Clin Mol Hepatol. 2016 Sep;22(3):309-318. doi: 10.3350/cmh.2016.0042. Epub 2016 Sep 25.

Abstract

There has been ongoing debate that the Milan criteria may be too strict that a significant number of patients who could benefit from liver transplantation (LT) might have been excluded. Based on this idea, various studies have been conducted to further expand the Milan criteria and give more HCC patients a chance of cure. In deceased donor LT (DDLT) setting, expansion of the criteria is relatively tempered because the results of LT for HCC should be comparable to those of patients with non-malignant indications. On the other hand, in living donor LT (LDLT) situation, liver grafts are not public resources. The acceptable target outcomes for LDLT might be much lower than those for DDLT. Patients with biologically favorable tumors might have excellent survivals after LT despite morphological advanced HCCs. Therefore, the significance and utility of biological tumor parameters for selecting suitable LT candidates have been increased to predict HCC recurrence after LT. Although there is no consensus regarding the use of prognostic biomarkers in LT selection criteria for HCC, the combination of conventional morphological parameters and new promising biomarkers could help us refine and expand the LT criteria for HCC in the near future.

摘要

一直存在这样的争论,即米兰标准可能过于严格,以至于大量可能从肝移植(LT)中获益的患者可能被排除在外。基于这一想法,已经开展了各种研究以进一步扩大米兰标准,让更多的肝癌患者有治愈的机会。在尸体供肝肝移植(DDLT)中,标准的扩大相对缓和,因为肝癌肝移植的结果应与非恶性指征患者的结果相当。另一方面,在活体供肝肝移植(LDLT)中,肝脏移植物不是公共资源。LDLT可接受的目标结果可能远低于DDLT。生物学行为良好的肿瘤患者尽管形态学上为晚期肝癌,但肝移植后可能有良好的生存率。因此,生物学肿瘤参数在选择合适的肝移植候选者以预测肝移植后肝癌复发方面的意义和实用性已有所增加。尽管在肝癌肝移植选择标准中使用预后生物标志物尚无共识,但传统形态学参数与新的有前景的生物标志物的结合可能有助于我们在不久的将来完善和扩大肝癌的肝移植标准。

相似文献

1
Liver transplantation for advanced hepatocellular carcinoma.
Clin Mol Hepatol. 2016 Sep;22(3):309-318. doi: 10.3350/cmh.2016.0042. Epub 2016 Sep 25.
2
Living donor liver transplantation for hepatocellular carcinoma.
Recent Results Cancer Res. 2013;190:165-79. doi: 10.1007/978-3-642-16037-0_11.
3
Section 5. Further expanding the criteria for HCC in living donor liver transplantation: when not to transplant: SNUH experience.
Transplantation. 2014 Apr 27;97 Suppl 8:S20-3. doi: 10.1097/01.tp.0000446269.20934.d3.
4
Expansion of the criteria for living donor liver transplantation for hepatocellular carcinoma.
Curr Opin Organ Transplant. 2016 Apr;21(2):231-7. doi: 10.1097/MOT.0000000000000294.
5
Liver transplantation for HCC: its role: Eastern and Western perspectives.
J Hepatobiliary Pancreat Sci. 2010 Jul;17(4):443-8. doi: 10.1007/s00534-009-0241-0. Epub 2009 Nov 3.
7
The stratifying value of Hangzhou criteria in liver transplantation for hepatocellular carcinoma.
PLoS One. 2014 Mar 27;9(3):e93128. doi: 10.1371/journal.pone.0093128. eCollection 2014.
8
Section 2. Small-for-size liver graft and hepatocellular carcinoma recurrence.
Transplantation. 2014 Apr 27;97 Suppl 8:S7-S10. doi: 10.1097/01.tp.0000446266.42019.28.
10
Liver transplantation beyond or downstaging within the Milan criteria for hepatocellular carcinoma.
Expert Rev Gastroenterol Hepatol. 2018 Mar;12(3):265-275. doi: 10.1080/17474124.2018.1417035. Epub 2017 Dec 28.

引用本文的文献

1
Living donor liver transplantation can be a rescue treatment for hepatocellular carcinoma.
Hepatobiliary Surg Nutr. 2024 Aug 1;13(4):742-744. doi: 10.21037/hbsn-24-198. Epub 2024 Jul 18.
4
Bromodomain-containing protein BRPF1 is a therapeutic target for liver cancer.
Commun Biol. 2021 Jul 20;4(1):888. doi: 10.1038/s42003-021-02405-6.
6
Achieving Complete Remission of Hepatocellular Carcinoma: A Significant Predictor for Recurrence-Free Survival after Liver Transplantation.
Can J Gastroenterol Hepatol. 2019 Jan 8;2019:5796074. doi: 10.1155/2019/5796074. eCollection 2019.
7
Multidisciplinary approach is associated with improved survival of hepatocellular carcinoma patients.
PLoS One. 2019 Jan 14;14(1):e0210730. doi: 10.1371/journal.pone.0210730. eCollection 2019.
8
Simple Maturation of Direct-Converted Hepatocytes Derived from Fibroblasts.
Tissue Eng Regen Med. 2017 Jun 23;14(5):579-586. doi: 10.1007/s13770-017-0064-z. eCollection 2017 Oct.
9
Sorafenib for Recurrent Hepatocellular Carcinoma after Liver Transplantation.
J Korean Med Sci. 2018 Oct 16;33(45):e286. doi: 10.3346/jkms.2018.33.e286. eCollection 2018 Nov 5.
10
Efficacy of Sorafenib for the Treatment of Post-Transplant Hepatocellular Carcinoma Recurrence.
J Korean Med Sci. 2018 Oct 12;33(45):e283. doi: 10.3346/jkms.2018.33.e283. eCollection 2018 Nov 5.

本文引用的文献

1
Liver transplantation for advanced hepatocellular carcinoma: how far can we go?
Hepat Oncol. 2015 Jan;2(1):19-28. doi: 10.2217/hep.14.34. Epub 2015 Jan 12.
2
Expansion of the criteria for living donor liver transplantation for hepatocellular carcinoma.
Curr Opin Organ Transplant. 2016 Apr;21(2):231-7. doi: 10.1097/MOT.0000000000000294.
4
Prediction of hepatocellular carcinoma biological behavior in patient selection for liver transplantation.
World J Gastroenterol. 2016 Jan 7;22(1):232-52. doi: 10.3748/wjg.v22.i1.232.
6
Liver transplantation as a management of hepatocellular carcinoma.
World J Hepatol. 2015 Jun 8;7(10):1347-54. doi: 10.4254/wjh.v7.i10.1347.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验