Is nelfinavir exposure associated with cancer incidence in HIV-positive individuals?

被引:6
|
作者
Boettiger, David C. [1 ]
Sabin, Caroline A. [2 ]
Grulich, Andrew [1 ]
Ryom, Lene [3 ]
Bonnet, Fabrice [4 ,5 ]
Reiss, Peter [6 ,7 ]
Monforte, Antonella d'arminio [8 ]
Kirk, Ole [3 ]
Phillips, Andrew [2 ]
Bower, Mark [9 ]
Fatkenheuer, Gerd [10 ]
Lundgren, Jens D. [3 ]
Law, Matthew [1 ]
机构
[1] UNSW Australia, Kirby Inst, Level 5 Wallace Wurth Bldg, Sydney, NSW 2052, Australia
[2] UCL, Res Dept Infect & Populat Hlth, London, England
[3] Univ Copenhagen, Rigshosp, Sect 2100, CHIP,Dept Infect Dis, DK-2100 Copenhagen, Denmark
[4] Univ Bordeaux, CHU Bordeaux, Talence, France
[5] Univ Bordeaux, INSERM U897, Talence, France
[6] Univ Amsterdam, Acad Med Ctr, Div Infect Dis, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[7] Univ Amsterdam, Acad Med Ctr, Dept Global Hlth, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[8] San Paolo Univ Hosp, Dept Hlth Sci, Milan, Italy
[9] Chelsea & Westminster Hosp, Natl Ctr HIV Malignancy, London, England
[10] Univ Hosp Cologne, Dept Internal Med 1, Cologne, Germany
基金
瑞士国家科学基金会; 新加坡国家研究基金会; 美国国家卫生研究院;
关键词
cancer; ethyl mesylate; HIV; Kaposi's sarcoma; nelfinavir; PROTEASE INHIBITOR NELFINAVIR; COMBINATION ANTIRETROVIRAL THERAPY; ENDOPLASMIC-RETICULUM STRESS; PREVENTING KAPOSIS-SARCOMA; MULTIPLE-MYELOMA CELLS; PHASE-I TRIAL; ETHYL METHANESULFONATE; MYOCARDIAL-INFARCTION; INFECTED PERSONS; RISK;
D O I
10.1097/QAD.0000000000001053
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: Nelfinavir exhibits potent anticancer properties against a range of tumours. However, in 2006/2007, nelfinavir supplies were accidently contaminated with a carcinogen. This analysis investigated the association between nelfinavir use and cancer risk in HIV-positive persons. Design: Observational cohort study. Methods: D:A:D study data was analysed using Poisson regression models to examine associations between cancer incidence and cumulative nelfinavir exposure, current nelfinavir exposure, and exposure to nelfinavir between 1 July 2006-30 June 2007. Results: A total of 42 006 individuals (50% white, 73% male) contributed 303 005 person-years of follow-up between 1 January 2004 and 1 February 2014. At study enrolment, median age was 40 [interquartile range (IQR) 33-46] years and 8305 individuals had a history of nelfinavir use [median duration 1.7 (IQR 0.7-3.4) years]. During follow-up, nelfinavir was used by 2476 individuals for a median of 1.7 (IQR 0.7-3.8) years; 1063 were exposed to nelfinavir between 1 July 2006 and 30 June 2007. Overall, 2279 cancers were diagnosed at a rate of 0.75 [95% confidence interval (95% CI) 0.72-0.78] per 100 person-years. Neither greater cumulative exposure to nelfinavir [adjusted risk ratio (aRR) 0.93 for every additional 5 years, 95% CI 0.82-1.06, P=0.26] nor current use of nelfinavir (aRR 0.98 vs other protease inhibitor use, 95% CI 0.68-1.41, P=0.92) were associated with cancer risk. The adjusted risk of cancer for participants exposed to nelfinavir between 1 July 2006 and 30 June 2007 compared to those receiving other treatment over this period was 1.07 (95% CI 0.78-1.46, P=0.68). Conclusion: Nelfinavir use was not associated with a lower cancer incidence than other protease inhibitor regimens. As of February 2014, exposure to the 2006/2007 contamination of nelfinavir does not appear to be associated with increased cancer incidence. Copyright (C) 2016 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:1629 / 1637
页数:9
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