Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Department of Health and Human Services, 6120 Executive Boulevard, EPS 7076, Rockville, MD 20892, USA.
Cancer Epidemiol Biomarkers Prev. 2010 May;19(5):1229-37. doi: 10.1158/1055-9965.EPI-09-1220. Epub 2010 Apr 20.
By assessing the spectrum of hematologic malignancies associated with solid-organ transplantation in the elderly, we provide information on the pathogenesis of lymphoid and myeloid neoplasms and the clinical manifestations of immunosuppression.
Using data from the U.S. Surveillance, Epidemiology, and End Results Medicare database, we identified 83,016 cases with a hematologic malignancy (age 66-99 years) and 166,057 population-based controls matched to cases by age, sex, and calendar year. Medicare claims were used to identify a history of solid-organ transplantation. We used polytomous logistic regression to calculate odds ratios (OR) comparing transplantation history among cases with various hematologic malignancy subtypes and controls, adjusting for the matching factors and race.
A prior solid-organ transplant was identified in 216 (0.26%) cases and 204 (0.12%) controls. Transplantation was associated with increased risk for non-Hodgkin lymphomas [OR, 2.13; 95% confidence interval (95% CI), 1.67-2.72], especially diffuse large B-cell lymphoma (OR, 3.29; 95% CI, 2.28-4.76), marginal zone lymphoma (OR, 2.48; 95% CI, 1.17-5.22), lymphoplasmacytic lymphoma (OR, 3.32; 95% CI, 1.41-7.81), and T-cell lymphoma (OR, 3.07; 95% CI, 1.56-6.06). Transplantation was also associated with elevated risk of Hodgkin lymphoma (OR, 2.53; 95% CI, 1.01-6.35) and plasma cell neoplasms (OR, 1.91; 95% CI, 1.24-2.93). Risks for myeloid neoplasms were also elevated (OR, 1.99; 95% CI, 1.41-2.81).
Solid-organ transplantation is associated with a wide spectrum of hematologic malignancies in the elderly. Risk was increased for four specific non-Hodgkin lymphoma subtypes for which a viral agent has been implicated, supporting an added role for immunosuppression.
Our results support monitoring for a wide spectrum of hematologic malignancies following solid-organ transplant.
通过评估与老年实体器官移植相关的血液系统恶性肿瘤谱,我们提供了关于淋巴细胞和髓系肿瘤发病机制以及免疫抑制临床表现的信息。
使用来自美国监测、流行病学和最终结果医疗保险数据库的数据,我们确定了 83016 例年龄在 66-99 岁之间患有血液系统恶性肿瘤(病例)和 166057 例按年龄、性别和日历年份与病例匹配的基于人群的对照。使用医疗保险索赔来确定实体器官移植的病史。我们使用多项逻辑回归来计算病例与各种血液系统恶性肿瘤亚型和对照之间的移植史的比值比(OR),并调整了匹配因素和种族。
在 216 例(0.26%)病例和 204 例(0.12%)对照中发现了先前的实体器官移植。移植与非霍奇金淋巴瘤的风险增加相关[比值比(OR),2.13;95%置信区间(95%CI),1.67-2.72],尤其是弥漫性大 B 细胞淋巴瘤(OR,3.29;95%CI,2.28-4.76)、边缘区淋巴瘤(OR,2.48;95%CI,1.17-5.22)、淋巴浆细胞淋巴瘤(OR,3.32;95%CI,1.41-7.81)和 T 细胞淋巴瘤(OR,3.07;95%CI,1.56-6.06)。移植还与霍奇金淋巴瘤(OR,2.53;95%CI,1.01-6.35)和浆细胞瘤(OR,1.91;95%CI,1.24-2.93)的风险增加相关。髓系肿瘤的风险也升高(OR,1.99;95%CI,1.41-2.81)。
实体器官移植与老年人群中广泛的血液系统恶性肿瘤有关。四种特定的非霍奇金淋巴瘤亚型的风险增加,其中已发现病毒因子的作用,这支持免疫抑制的额外作用。
我们的结果支持在实体器官移植后监测广泛的血液系统恶性肿瘤。