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根据多达七条标准的肝细胞癌肝移植术后复发情况。

Recurrence after liver transplantation for hepatocellular carcinoma according to up-to-seven criteria.

作者信息

Gugenheim Jean, Bredt Luis César, Iannelli Antonio, Decaens Thomas, Roudot-Thoraval Francoise, Meyer Carole, Durand Francois, Bernard Pierre-Henri, Boillot Olivier, Sulpice Laurent, Calmus Yvon, Hardwigsen Jean, Ducerf Christian, Pageaux Georges-Philippe, Dharancy Sebastien, Chazouilleres Olivier, Cherqui Daniel, Duvoux Christophe, Hadni-Bresson Solange

出版信息

Hepatogastroenterology. 2013 Jun;60(124):799-806. doi: 10.5754/hge12997. Epub 2013 Jun 6.

DOI:10.5754/hge12997
PMID:23742832
Abstract

BACKGROUND/AIMS: The Up7 criteria for HCC have recently emerged to identify potential candidates for OLT. The aim of this study was to assess the validity of the Up7 criteria according to the pathological analysis of the explanted livers.

METHODOLOGY

For recurrence risk calculation 669 HCC transplanted patients were classified according to both the pathological Milan and Up7 criteria. In order to identify potential predictors of recurrence, selected biological tumor markers and morphological features were then tested by Cox regression.

RESULTS

The 5-year HCC recurrence rate for the Milan out/Up7 in subgroup (n=87), was significantly higher than patients meeting Milan criteria (n=299), 15.8% vs. 9.4% (p=0.0290). For patients within the Up7 criteria (n=383), only pre-OLT AFP level >1000ng/mL and microvascular invasion were significant predictors for recurrence, and for those beyond the Up7 criteria (n=286), pre-OLT AFP level >1000ng/mL, poor differentiation grade and microvascular invasion remained significant.

CONCLUSIONS

Compared to the current Milan staging system, HCC patients within the pathological Up7 criteria were associated with a higher, but acceptable risk of recurrence after OLT, and along with tumor burden, other parameters can potentially be used for further refinement of HCC staging, such as AFP levels and microvascular invasion.

摘要

背景/目的:用于肝细胞癌(HCC)的Up7标准最近已出现,以识别肝移植(OLT)的潜在候选者。本研究的目的是根据移植肝脏的病理分析评估Up7标准的有效性。

方法

为了计算复发风险,669例接受HCC移植的患者根据病理米兰标准和Up7标准进行分类。为了确定复发的潜在预测因素,然后通过Cox回归测试选定的生物肿瘤标志物和形态学特征。

结果

米兰标准不符合/Up7标准亚组(n = 87)的5年HCC复发率显著高于符合米兰标准的患者(n = 299),分别为15.8%和9.4%(p = 0.0290)。对于符合Up7标准的患者(n = 383),仅肝移植前甲胎蛋白(AFP)水平>1000ng/mL和微血管侵犯是复发的显著预测因素,而对于超出Up7标准的患者(n = 286),肝移植前AFP水平>1000ng/mL、低分化等级和微血管侵犯仍然具有显著性。

结论

与当前的米兰分期系统相比,符合病理Up7标准的HCC患者肝移植后复发风险较高但仍可接受,并且除了肿瘤负荷外,其他参数如AFP水平和微血管侵犯可能可用于进一步完善HCC分期。

相似文献

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Recurrence after liver transplantation for hepatocellular carcinoma according to up-to-seven criteria.根据多达七条标准的肝细胞癌肝移植术后复发情况。
Hepatogastroenterology. 2013 Jun;60(124):799-806. doi: 10.5754/hge12997. Epub 2013 Jun 6.
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Rate of tumor growth predicts recurrence of hepatocellular carcinoma after liver transplantation in patients beyond Milan or UCSF criteria.肿瘤生长速率可预测超出米兰或加州大学旧金山分校标准的患者肝移植后肝细胞癌的复发情况。
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Recurrent hepatocellular carcinoma after transplantation: use of a pathological score on explanted livers to predict recurrence.肝移植后复发性肝细胞癌:利用移植肝的病理评分预测复发情况。
Liver Transpl. 2007 Apr;13(4):543-51. doi: 10.1002/lt.21078.
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Multifocal manifestation does not affect vascular invasion of hepatocellular carcinoma: implications for patient selection in liver transplantation.多灶性表现不影响肝细胞癌的血管侵犯:对肝移植患者选择的启示
Clin Transplant. 2007 Nov-Dec;21(6):696-701. doi: 10.1111/j.1399-0012.2007.00707.x.
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Liver transplantation criteria for hepatocellular carcinoma should be expanded: a 22-year experience with 467 patients at UCLA.肝细胞癌的肝移植标准应扩大:加州大学洛杉矶分校467例患者的22年经验。
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Liver transplantation for hepatocellular carcinoma: a model including α-fetoprotein improves the performance of Milan criteria.肝癌肝移植:包含甲胎蛋白的模型可改善米兰标准的性能。
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Pretransplantation α-fetoprotein slope and milan criteria: strong predictors of hepatocellular carcinoma recurrence after transplantation.移植前甲胎蛋白斜率和米兰标准:移植后肝细胞癌复发的强预测因子。
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Surgical treatment of hepatocellular carcinoma beyond Milan criteria. Results of liver resection, salvage transplantation, and primary liver transplantation.米兰标准以外的肝细胞癌的外科治疗。肝切除、挽救性移植和原位肝移植的结果。
Ann Surg Oncol. 2008 May;15(5):1383-91. doi: 10.1245/s10434-008-9851-z. Epub 2008 Mar 5.

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