Opelz Gerhard, Döhler Bernd
Department of Transplantation Immunology, University of Heidelberg, Heidelberg, Germany.
Am J Transplant. 2004 Feb;4(2):222-30. doi: 10.1046/j.1600-6143.2003.00325.x.
We used the Collaborative Transplant Study database to analyze the incidence, risk, and impact of malignant lymphomas in approximately 200,000 organ transplant recipients. Over a 10-year period, the risk in renal transplant recipients was 11.8-fold higher than that in a matched nontransplanted population (p<0.0001). The majority of lymphomas were diagnosed after the first post-transplant year. Heart-lung transplants showed the highest relative risk (RR 239.5) among different types of organ transplants. In kidney recipients, immunosuppression with cyclosporine did not confer added risk compared with azathioprine/steroid treatment, whereas treatment with FK506 increased the risk approximately twofold. Induction therapy with OKT3 or ATG, but not with anti-IL2 receptor antibodies, increased the risk of lymphoma during the first year. Antirejection therapy with OKT3 or ATG also increased the risk. First-year mortality in renal and heart transplant patients with lymphoma was approximately 40% and 50%, respectively, and showed no improvement in recent years. A pattern of preferential localization to the vicinity of the transplant was noted, and the prognosis of the patient was related to localization. This study highlights the continuing risk for lymphoma with time post-transplantation, the contribution of immunosuppression to increased risk, and continuing poor outcomes in patients with post-transplant lymphoma.
我们利用协作移植研究数据库分析了约200,000名器官移植受者中恶性淋巴瘤的发病率、风险及影响。在10年期间,肾移植受者的风险比匹配的未移植人群高11.8倍(p<0.0001)。大多数淋巴瘤在移植后的第一年之后被诊断出来。在不同类型的器官移植中,心肺移植显示出最高的相对风险(RR 239.5)。在肾移植受者中,与硫唑嘌呤/类固醇治疗相比,环孢素免疫抑制并未带来额外风险,而使用FK506治疗使风险增加约两倍。使用OKT3或抗胸腺细胞球蛋白进行诱导治疗,但不包括抗IL2受体抗体,会增加第一年患淋巴瘤的风险。使用OKT3或抗胸腺细胞球蛋白进行抗排斥治疗也会增加风险。肾移植和心脏移植淋巴瘤患者的第一年死亡率分别约为40%和50%,且近年来并无改善。观察到淋巴瘤有优先定位于移植部位附近的模式,且患者的预后与定位有关。这项研究强调了移植后随着时间推移淋巴瘤持续存在的风险、免疫抑制对风险增加的作用以及移植后淋巴瘤患者持续不佳的预后。