Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland 20892, USA.
Transfusion. 2010 Oct;50(10):2249-57. doi: 10.1111/j.1537-2995.2010.02692.x. Epub 2010 Oct 4.
Blood transfusions are associated with viral transmission and immunomodulation, perhaps increasing subsequent risk of hematologic malignancies (HMs). Prior studies of transfusion recipients have lacked details on specific HM subtypes.
Risk of HM after blood transfusion was evaluated in a US population-based case-control study (77,488 elderly HM cases identified through cancer registries, 154,509 controls). Transfusions were identified using linked Medicare hospitalization claims. Polytomous logistic regression was used to calculate odds ratios (ORs) associating transfusion and HM subtypes by features suggestive of a causal relationship.
A history of transfusion was present in 7.9% of HM cases versus 5.9% of controls. Associations for most HM subtypes suggested reverse causality: ORs were elevated only during the shortest latency periods; ORs for unspecified anemia and gastrointestinal bleeding, which may be related to undiagnosed HM, were stronger than for surgeries, which are unlikely to be related to HM; and/or there was no dose response. In contrast, risk for lymphoplasmacytic lymphoma (1397 cases) was elevated at long latency (OR, 1.56 at 10+ years after transfusion), after transfusions related to surgeries (OR, 1.22-1.47), and in a dose-response relationship with number of transfusion-related hospitalizations (OR, 1.53 with one hospitalization; OR, 1.80 with two or more hospitalizations, p trend < 0.0001). Risk for marginal zone lymphoma (1915 cases) was also elevated at 10+ years after transfusion (OR, 1.80).
Consistent with prior studies, blood transfusions did not increase risk of most HM subtypes. Patterns of elevated risk for lymphoplasmacytic and marginal zone lymphomas suggest an etiologic role for transfusion.
输血与病毒传播和免疫调节有关,可能会增加随后发生血液系统恶性肿瘤(HMs)的风险。先前对输血受者的研究缺乏对特定 HM 亚型的详细信息。
我们在美国进行了一项基于人群的病例对照研究(通过癌症登记处确定了 77488 例老年 HM 病例,154509 例对照),评估了输血后 HM 的风险。通过链接的 Medicare 住院索赔确定输血情况。多分类逻辑回归用于计算与输血和 HM 亚型相关的比值比(ORs),这些亚型的特征提示存在因果关系。
7.9%的 HM 病例有输血史,而对照组为 5.9%。大多数 HM 亚型的关联表明存在反向因果关系:仅在最短潜伏期内,OR 升高;未明确的贫血和胃肠道出血的 OR 高于手术,这可能与未确诊的 HM 有关,而手术不太可能与 HM 有关;并且/或者不存在剂量反应。相比之下,淋巴浆细胞淋巴瘤(1397 例)的风险在潜伏期较长时(输血后 10 年以上的 OR 为 1.56)、与手术相关的输血(OR 为 1.22-1.47)以及与输血相关的住院次数呈剂量反应关系时(OR 为 1.53 次住院;OR 为 1.80 次以上住院,p 趋势 <0.0001)较高。边缘区淋巴瘤(1915 例)的风险也在输血后 10 年以上升高(OR 为 1.80)。
与先前的研究一致,输血并未增加大多数 HM 亚型的风险。淋巴浆细胞性和边缘区淋巴瘤风险升高的模式表明输血具有病因作用。