Gibson Todd M, Morton Lindsay M, Shiels Meredith S, Clarke Christina A, Engels Eric A
aDivision of Cancer Epidemiology and Genetics bCancer Prevention Fellowship Program, National Cancer Institute, Bethesda, Maryland cCancer Prevention Institute of California, Fremont, California, USA. *Current affiliation: Department of Epidemiology and Cancer Control, St Jude Children's Research Hospital, Memphis, Tennessee, USA.
AIDS. 2014 Sep 24;28(15):2313-8. doi: 10.1097/QAD.0000000000000428.
HIV-infected people have greatly elevated risk of non-Hodgkin lymphoma (NHL), particularly the AIDS-defining NHL subtypes: diffuse large B-cell lymphoma, Burkitt lymphoma and primary lymphomas arising in the central nervous system. The goals of this analysis were to comprehensively describe risks of NHL subtypes, especially those not well studied, among HIV/AIDS patients; examine risks specifically in the HAART era; and distinguish risks in HIV-infected individuals prior to diagnosis with AIDS.
Population-based registry linkage study.
We used data from the US HIV/AIDS Cancer Match Study from 1996 to 2010 (N = 273 705) to calculate standardized incidence ratios (SIRs) comparing subtype-specific NHL risks in HIV-infected people to those in the general population, and used Poisson regression to test for differences in SIRs between the HIV-only and AIDS periods.
NHL risk was elevated 11-fold compared to the general population, but varied substantially by subtype. AIDS-defining NHL subtypes comprised the majority, and risks were high (SIRs ≥17), but risks were also increased for some T-cell lymphomas (SIRs = 3.6-14.2), marginal zone lymphoma (SIR = 2.4), lymphoplasmacytic lymphoma/Waldenström macroglobulinemia (SIR = 3.6), and acute lymphoblastic leukemia/lymphoma (SIR = 2.4).
HIV-infected people in the HAART era continue to have elevated risk of AIDS-defining NHL subtypes, highlighting the contribution of moderate and severe immunosuppression to their cause. Whereas non-AIDS-defining subtypes are much less common, immunosuppression or other dysregulated immune states likely play a role in the cause of some T-cell lymphomas, marginal zone lymphoma, lymphoplasmacytic lymphoma/Waldenström macroglobulinemia, and acute lymphoblastic leukemia/lymphoma.
HIV感染者患非霍奇金淋巴瘤(NHL)的风险大幅升高,尤其是符合艾滋病定义的NHL亚型:弥漫性大B细胞淋巴瘤、伯基特淋巴瘤以及中枢神经系统原发性淋巴瘤。本分析的目的是全面描述HIV/AIDS患者中NHL亚型的风险,尤其是那些研究较少的亚型;研究在高效抗逆转录病毒治疗(HAART)时代的特定风险;并区分艾滋病诊断前HIV感染者的风险。
基于人群的登记链接研究。
我们使用了1996年至2010年美国HIV/AIDS癌症匹配研究的数据(N = 273705),计算标准化发病率比(SIR),以比较HIV感染者与普通人群中特定亚型NHL的风险,并使用泊松回归检验仅感染HIV时期和艾滋病时期SIR的差异。
与普通人群相比,NHL风险升高了11倍,但各亚型差异很大。符合艾滋病定义的NHL亚型占多数,风险很高(SIR≥17),但一些T细胞淋巴瘤(SIR = 3.6 - 14.2)、边缘区淋巴瘤(SIR = 2.4)、淋巴浆细胞淋巴瘤/华氏巨球蛋白血症(SIR = 3.6)以及急性淋巴细胞白血病/淋巴瘤(SIR = 2.4)的风险也有所增加。
HAART时代的HIV感染者患符合艾滋病定义的NHL亚型的风险仍然很高,突出了中度和重度免疫抑制对其病因的作用。虽然不符合艾滋病定义的亚型要少见得多,但免疫抑制或其他失调的免疫状态可能在一些T细胞淋巴瘤、边缘区淋巴瘤、淋巴浆细胞淋巴瘤/华氏巨球蛋白血症以及急性淋巴细胞白血病/淋巴瘤的病因中起作用。