接受三联免疫抑制药物的心脏和心肺移植受者肿瘤发生率低。

The Journal of heart transplantation Pub Date : 1990-11-01
M T Olivari, R A Diekmann, S H Kubo, E Braunlin, S W Jamieson, W S Ring
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引用次数: 0

摘要

实体器官移植后肿瘤发生的风险明显增加免疫抑制治疗。据报道,接受环孢素治疗的心脏移植受者中有13%发生淋巴瘤,33%的心肺移植受者发生淋巴瘤,皮肤癌的发病率在6%至16%之间。在三联免疫抑制药物中使用较低负荷和维持剂量的环孢素,移植后肿瘤的发生率尚不清楚。从1983年12月到1988年8月,明尼苏达大学进行了134例心脏和7例心肺移植手术。所有患者均接受环孢素、硫唑嘌呤和强的松联合治疗。心脏受者1年生存率为94%,3年生存率为90%。急性排斥反应在3个月时为9%,1年和3年时为12%。只有2例患者在心脏移植后发生b细胞淋巴瘤,发病率为1.5%。急性排斥反应的发作和平均环孢素血水平不能预测移植后淋巴瘤的发生。皮肤癌的发生率为6.4%。心肺移植受者无肿瘤发生。所有肿瘤均发生在50岁以上的患者中。我们的数据表明,在接受三联免疫抑制药物的心脏和心肺移植受者中,发生淋巴增生性疾病的风险降低了,但基底细胞癌的风险没有降低。年龄较大的受者可能有更高的风险,提示在该组中应考虑低剂量的免疫抑制治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low incidence of neoplasia in heart and heart-lung transplant recipients receiving triple-drug immunosuppression.

The risk of neoplasias developing after solid organ transplantation is markedly increased by immunosuppressive therapy. Lymphoma has been reported to develop in 13% of heart and in 33% of heart-lung transplant recipients treated with cyclosporine, and the incidence of skin carcinoma ranges between 6% and 16%. The incidence of posttransplant neoplasias with the use of lower loading and maintenance doses of cyclosporine as used in triple-drug immunosuppression is unknown. From December 1983 through August 1988, 134 heart and seven heart-lung transplants were performed at the University of Minnesota. All patients received a combination of cyclosporine, azathioprine, and prednisone. Survival was 94% at 1 and 90% at 3 years in heart recipients. Probability of acute rejection was 9% at 3 months and 12% at 1 and 3 years. B-cell lymphoma developed after heart transplant in only two patients for an incidence of 1.5%. Episodes of acute rejection and mean cyclosporine blood level did not predict the occurrence of posttransplant lymphoma. The incidence of skin carcinoma was 6.4%. No neoplasia occurred in heart-lung transplant recipients. All neoplasias were observed in patients older than 50 years. Our data indicate that the risk for developing lymphoproliferative disorders, but not for basal cell carcinoma, is reduced in heart and heart-lung transplant recipients receiving triple-drug immunosuppression. Older recipients may be at increased risk, suggesting that lower doses of immunosuppressive therapy should be considered in this group.

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