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移植后恶性肿瘤

Malignancy after transplantation.

作者信息

Buell Joseph F, Gross Thomas G, Woodle E Steve

机构信息

Israel Penn International Transplant Tumor Registry, University of Cincinnati, Cincinnati, OH 45267-0558, USA.

出版信息

Transplantation. 2005 Oct 15;80(2 Suppl):S254-64. doi: 10.1097/01.tp.0000186382.81130.ba.

Abstract

As newer immunosuppressive regimens have steadily reduced the incidence of acute rejection and have extended the life expectancy of allograft recipients, posttransplant malignancy has become an important cause of mortality. In fact, it is expected that cancer will surpass cardiovascular complications as the leading cause of death in transplant patients within the next 2 decades. An understanding of the underlying pathobiology and how to minimize cancer risks in transplant recipients are essential. The etiology of posttransplant malignancy is believed to be multifactorial and likely involves impaired immunosurveillance of neoplastic cells as well as depressed antiviral immune activity with a number of common posttransplant malignancies being viral-related. Although calcineurin inhibitors and azathioprine have been linked with posttransplant malignancies, newer agents such as mycophenolate mofetil and sirolimus have not and indeed may have antitumor properties. Long-term data are needed to determine if the use of these agents will ultimately lower the mortality due to malignancy for transplant recipients.

摘要

随着更新的免疫抑制方案稳步降低了急性排斥反应的发生率,并延长了同种异体移植受者的预期寿命,移植后恶性肿瘤已成为重要的死亡原因。事实上,预计在未来20年内,癌症将超过心血管并发症,成为移植患者的主要死亡原因。了解潜在的病理生物学以及如何将移植受者的癌症风险降至最低至关重要。移植后恶性肿瘤的病因被认为是多因素的,可能涉及对肿瘤细胞的免疫监视受损以及抗病毒免疫活性降低,许多常见的移植后恶性肿瘤与病毒有关。虽然钙调神经磷酸酶抑制剂和硫唑嘌呤与移植后恶性肿瘤有关,但诸如霉酚酸酯和西罗莫司等新型药物则不然,实际上可能具有抗肿瘤特性。需要长期数据来确定使用这些药物是否最终会降低移植受者因恶性肿瘤导致的死亡率。

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