Exposure to antiretroviral therapy and risk of cancer in HIV-infected persons

被引:61
作者
Chao, Chun [2 ]
Leyden, Wendy A.
Xu, Lanfang [2 ]
Horberg, Michael A. [3 ]
Klein, Daniel [4 ]
Towner, William J. [5 ]
Quesenberry, Charles P., Jr.
Abrams, Donald I. [6 ,7 ]
Silverberg, Michael J. [1 ]
机构
[1] Kaiser Permanente No Calif, Div Res, Oakland, CA 94612 USA
[2] Kaiser Permanente So Calif, Pasadena, CA USA
[3] Midatlantic Permanente Res Inst, Rockville, MD USA
[4] Kaiser Permanente No Calif, Hayward, CA USA
[5] Kaiser Permanente So Calif, Los Angeles, CA USA
[6] San Francisco Gen Hosp, San Francisco, CA 94110 USA
[7] Univ Calif San Francisco, San Francisco, CA 94143 USA
关键词
cancer; cohort study; combination antiretroviral therapy; HIV infection; nonnucleotide reverse transcriptase inhibitor; protease inhibitor; HUMAN-IMMUNODEFICIENCY-VIRUS; AIDS-DEFINING MALIGNANCIES; NON-HODGKINS-LYMPHOMA; CO3 AQUITAINE COHORT; PROTEASE INHIBITOR; UNITED-STATES; IN-VITRO; PROSTATE-CANCER; KAPOSIS-SARCOMA; CELLS;
D O I
10.1097/QAD.0b013e32835935b3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: The incidence of certain non-AIDS-defining cancers (NADCs) in HIV patients has been reported to have increased in the combination antiretroviral therapy (ART) era. Studies are needed to directly evaluate the effect of ART use on cancer risk. Design: We followed 12 872 HIV-infected Kaiser Permanente members whose complete ART history was known for incident cancers between 1996 and 2008. Methods: Cancers, identified from Surveillance, Epidemiology, and End Results (SEER)based cancer registries, were grouped as ADCs, infection-related NADCs, or infection-unrelated NADCs. We also evaluated the most common individual cancer types. Rate ratios for ART use (yes/no) and cumulative duration of any ART, protease inhibitor, and nonnucleotide reverse transcriptase inhibitor (NNRTI) therapy were obtained from Poisson models adjusting for demographics, pretreatment or recent CD4 cell count and HIV RNA levels, years known HIV-infected, prior antiretroviral use, HIV risk, smoking, alcohol/drug abuse, overweight/obesity, and calendar year. Results: The cohort experienced 32 368 person-years of ART, 21 249 person-years of protease inhibitor therapy, and 15 643 person-years of NNRTI therapy. The mean follow-up duration was 4.5 years. ADC rates decrease with increased duration of ART use [rate ratio per year = 0.61 (95% confidence interval 0.56-0.66)]; the effect was similar by therapy class. ART, protease inhibitor, or NNRTI therapy duration was not associated with infection-related or infection-unrelated NADC [rate ratio per year ART = 1.00 (0.91-1.11) and 0.96 (0.90-1.01), respectively], except a higher anal cancer risk with longer protease inhibitor therapy [rate ratio per year = 1.16 (1.02-1.31)]. Conclusion: No therapy class-specific effect was found for ADC. ART exposure was generally not associated with NADC risk, except for long-term use of protease inhibitor, which might be associated with increased anal cancer risk. (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
引用
收藏
页码:2223 / 2231
页数:9
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