Park Lesley S, Tate Janet P, Sigel Keith, Rimland David, Crothers Kristina, Gibert Cynthia, Rodriguez-Barradas Maria C, Goetz Matthew Bidwell, Bedimo Roger J, Brown Sheldon T, Justice Amy C, Dubrow Robert
aStanford University School of Medicine, Stanford, California bVeterans Affairs Connecticut Healthcare System, West Haven cYale School of Medicine, New Haven, Connecticut dIcahn School of Medicine at Mt. Sinai, New York, New York eAtlanta Veterans Affairs Medical Center fEmory University School of Medicine, Atlanta, Georgia gUniversity of Washington School of Medicine, Seattle, Washington hWashington DC Veterans Affairs Medical Center iGeorge Washington University School of Medicine and Health Sciences, Washington, District of Columbia jMichael E. DeBakey Veterans Affairs Medical Center kBaylor College of Medicine, Houston, Texas lVeterans Affairs Greater Los Angeles Healthcare System mDavid Geffen School of Medicine, University of California, Los Angeles, California nVeterans Affairs North Texas Healthcare System oUniversity of Texas Southwestern Medical Center, Dallas, Texas pJames J. Peters Veterans Affairs Medical Center, New York, New York qYale School of Public Health, New Haven, Connecticut, USA.
AIDS. 2016 Jul 17;30(11):1795-806. doi: 10.1097/QAD.0000000000001112.
Utilizing the Veterans Aging Cohort Study, the largest HIV cohort in North America, we conducted one of the few comprehensive comparisons of cancer incidence time trends in HIV-infected (HIV+) versus uninfected persons during the antiretroviral therapy (ART) era.
Prospective cohort study.
We followed 44 787 HIV+ and 96 852 demographically matched uninfected persons during 1997-2012. We calculated age-, sex-, and race/ethnicity-standardized incidence rates and incidence rate ratios (IRR, HIV+ versus uninfected) over four calendar periods with incidence rate and IRR period trend P values for cancer groupings and specific cancer types.
We observed 3714 incident cancer diagnoses in HIV+ and 5760 in uninfected persons. The HIV+ all-cancer crude incidence rate increased between 1997-2000 and 2009-2012 (P trend = 0.0019). However, after standardization, we observed highly significant HIV+ incidence rate declines for all cancer (25% decline; P trend <0.0001), AIDS-defining cancers (55% decline; P trend <0.0001), nonAIDS-defining cancers (NADC; 15% decline; P trend = 0.0003), and nonvirus-related NADC (20% decline; P trend <0.0001); significant IRR declines for all cancer (from 2.0 to 1.6; P trend <0.0001), AIDS-defining cancers (from 19 to 5.5; P trend <0.0001), and nonvirus-related NADC (from 1.4 to 1.2; P trend = 0.049); and borderline significant IRR declines for NADC (from 1.6 to 1.4; P trend = 0.078) and virus-related NADC (from 4.9 to 3.5; P trend = 0.071).
Improved HIV care resulting in improved immune function most likely contributed to the HIV+ incidence rate and the IRR declines. Further promotion of early and sustained ART, improved ART regimens, reduction of traditional cancer risk factor (e.g. smoking) prevalence, and evidence-based screening could contribute to future cancer incidence declines among HIV+ persons.
利用北美最大的HIV队列——退伍军人老龄化队列研究,我们在抗逆转录病毒治疗(ART)时代,对HIV感染者(HIV+)与未感染者的癌症发病率时间趋势进行了为数不多的全面比较之一。
前瞻性队列研究。
我们在1997年至2012年期间跟踪了44787名HIV+患者和96852名人口统计学匹配的未感染者。我们计算了四个日历期内按年龄、性别和种族/族裔标准化的发病率和发病率比(IRR,HIV+与未感染者相比),并得出癌症分组和特定癌症类型的发病率和IRR时期趋势P值。
我们观察到HIV+患者中有3714例癌症诊断为新发,未感染者中有5760例。HIV+患者的所有癌症粗发病率在1997 - 2000年至2009 - 2012年期间有所上升(P趋势 = 0.0019)。然而,标准化后,我们观察到HIV+患者的所有癌症发病率显著下降(下降25%;P趋势<0.0001),定义艾滋病的癌症(下降55%;P趋势<0.0001),非定义艾滋病的癌症(NADC;下降15%;P趋势 = 0.0003),以及非病毒相关的NADC(下降20%;P趋势<0.0001);所有癌症的IRR显著下降(从2.0降至1.6;P趋势<0.0001),定义艾滋病的癌症(从19降至5.5;P趋势<0.0001),以及非病毒相关的NADC(从1.4降至1.2;P趋势 = 0.049);NADC(从1.6降至1.4;P趋势 = 0.078)和病毒相关NADC(从4.9降至3.5;P趋势 = 0.071)的IRR下降接近显著。
HIV治疗的改善导致免疫功能增强,很可能是HIV+患者发病率和IRR下降的原因。进一步推广早期和持续的ART、改进ART方案、降低传统癌症危险因素(如吸烟)的流行率以及基于证据的筛查,可能有助于未来HIV+患者癌症发病率的下降。