Pluda J M, Venzon D J, Tosato G, Lietzau J, Wyvill K, Nelson D L, Jaffe E S, Karp J E, Broder S, Yarchoan R
Medicine Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
J Clin Oncol. 1993 Jun;11(6):1099-107. doi: 10.1200/JCO.1993.11.6.1099.
To investigate the occurrence of non-Hodgkin's lymphoma (NHL) in human immunodeficiency virus (HIV)-infected patients receiving long-term antiretroviral therapy and factors associated with the development of these lymphomas.
The charts of 55 patients with advanced HIV infection receiving zidovudine (formerly known as azidothymidine [AZT])-based therapy and 61 patients receiving dideoxyinosine (ddI) were examined for the occurrence of NHL. Stored samples from the AZT-based treatment cohort were examined retrospectively for parameters predictive of the subsequent development of lymphoma.
Eight of 55 patients receiving AZT-based therapy developed NHL, yielding an estimated probability of 12% (95% confidence interval [CI], 4.7% to 27.1%) after 24 months, and 29.2% (95% CI, 15.2% to 48.7%) after 36 months. Four of 61 patients receiving ddI developed NHL, yielding a 6.2% (95% CI, 2.1% to 17%) estimated probability after 24 months, and 9.5% (95% CI, 3.6% to 22.8%) after 36 months. The difference between these cohorts was not significant (two-tailed P [P2] = .13). Patients with less than 50 CD4 cells/microL developed NHL at a significantly higher rate (P2 = .0085). This was particularly true for patients who presented with primary CNS lymphoma (PCNSL). For patients receiving AZT-based therapy, pretreatment serum interleukin-6 (IL-6) levels were somewhat higher in those who subsequently developed NHL than in those who did not (P2 = .048).
HIV-infected patients with profound immunodeficiency, especially those with less than 50 CD4 cells/microL, are at substantial risk of developing NHL and particularly PCNSL. Additional studies are needed to define the role of other factors such as IL-6 in the pathogenesis of these opportunistic tumors.
调查接受长期抗逆转录病毒治疗的人类免疫缺陷病毒(HIV)感染患者中非霍奇金淋巴瘤(NHL)的发生率以及与这些淋巴瘤发生相关的因素。
检查了55例接受以齐多夫定(曾称为叠氮胸苷[AZT])为基础治疗的晚期HIV感染患者以及61例接受双脱氧肌苷(ddI)治疗患者的病历,以了解NHL的发生情况。对以AZT为基础治疗队列中储存的样本进行回顾性检查,以寻找预测淋巴瘤后续发生的参数。
55例接受以AZT为基础治疗的患者中有8例发生NHL,24个月后的估计发生率为12%(95%置信区间[CI],4.7%至27.1%),36个月后为29.2%(95%CI,15.2%至48.7%)。61例接受ddI治疗的患者中有4例发生NHL,24个月后的估计发生率为6.2%(95%CI,2.1%至17%),36个月后为9.5%(95%CI,3.6%至22.8%)。这两个队列之间的差异不显著(双侧P[P2]=0.13)。CD4细胞计数低于50个/微升的患者发生NHL的比率显著更高(P2=0.0085)。对于原发性中枢神经系统淋巴瘤(PCNSL)患者尤其如此。对于接受以AZT为基础治疗的患者,随后发生NHL的患者预处理血清白细胞介素-6(IL-6)水平略高于未发生NHL的患者(P2=0.048)。
免疫严重缺陷的HIV感染患者,尤其是CD4细胞计数低于50个/微升的患者,发生NHL尤其是PCNSL的风险很大。需要进一步研究以确定其他因素如IL-6在这些机会性肿瘤发病机制中的作用。