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Malignancy after transplantation.

机译:移植后恶性肿瘤。

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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.
机译:随着更新的免疫抑制方案稳定地降低了急性排斥反应的发生率并延长了同种异体移植受体的预期寿命,移植后恶性肿瘤已成为导致死亡的重要原因。实际上,预计在接下来的20年内,癌症将超过心血管并发症,成为移植患者死亡的主要原因。必须了解潜在的病理生物学以及如何最大程度地减少移植受者的癌症风险。移植后恶性肿瘤的病因被认为是多因素的,并且可能涉及肿瘤细胞的免疫监视受损以及抗病毒免疫活性降低,其中许多常见的移植后恶性肿瘤与病毒有关。尽管钙调神经磷酸酶抑制剂和硫唑嘌呤与移植后的恶性肿瘤有关,但较新的药物如霉酚酸酯和西罗莫司却没有,甚至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由于移植受者的恶性肿瘤导致的死亡率。

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