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影响接受抗逆转录病毒治疗的严重人类免疫缺陷病毒感染患者非霍奇金淋巴瘤发生的因素。

Parameters affecting the development of non-Hodgkin's lymphoma in patients with severe human immunodeficiency virus infection receiving antiretroviral therapy.

作者信息

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

机构信息

Medicine Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

J Clin Oncol. 1993 Jun;11(6):1099-107. doi: 10.1200/JCO.1993.11.6.1099.

DOI:10.1200/JCO.1993.11.6.1099
PMID:8099121
Abstract

PURPOSE

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.

PATIENTS AND METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

目的

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。

患者与方法

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。

结果

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)。

结论

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。

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