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Risk of cervical precancer and cancer among HIV-infected women with normal cervical cytology and no evidence of oncogenic HPV infection

机译:在宫颈细胞学检查正常且无致癌HPV感染迹象的HIV感染妇女中,宫颈癌和癌变的风险

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Context: US cervical cancer screening guidelines for human immunodeficiency virus (HIV)-uninfected women 30 years or older have recently been revised, increasing the suggested interval between Papanicolaou (Pap) tests from 3 years to 5 years among those with normal cervical cytology (Pap test) resultswhotest negative for oncogenic human papilloma-virus (HPV). Whether a 3-year or 5-year screening interval could be used in HIV-infected women who are cytologically normal and oncogenic HPV-negative is unknown. Objective: To determine the risk of cervical precancer or cancer defined cytologically (high-grade squamous intraepithelial lesions or greater [HSIL+]) or histologically (cervical intraepithelial neoplasia 2 or greater [CIN-2+]), as 2 separate end points, in HIV-infected women and HIV-uninfected women who at baseline had a normal Pap test result and were negative for oncogenic HPV. Design, Setting, and Participants: Participants included 420 HIV-infected women and 279 HIV-uninfected women with normal cervical cytology at their enrollment in a multi-institutional US cohort of the Women's Interagency HIV Study, between October 1, 2001, and September 30, 2002, with follow-up through April 30, 2011. Semi-annual visits at 6 clinical sites included Pap testing and, if indicated, cervical biopsy. Cervicovaginal lavage specimens from enrollment were tested for HPV DNA using polymerase chain reaction. The primary analysis was truncated at 5 years of follow-up. Main Outcome Measure: Five-year cumulative incidence of cervical precancer and cancer. Results: No oncogenic HPV was detected in 369 (88% [95% CI,84%-91%]) HIV-infected women and 255 (91% [95% CI, 88%-94%]) HIV-uninfected women with normal cervical cytology at enrollment. Among these oncogenic HPV-negative women, 2 cases of HSIL+ were observed; an HIV-uninfected woman and an HIV-infected woman with a CD4 cell count of 500 cells/μL or greater. Histologic data were obtained from 4 of the 6 clinical sites. There were 6 cases of CIN-2+ in 145 HIV-uninfected women (cumulative incidence, 5% [95% CI, 1%-8%]) and 9 cases in 219 HIV-infected women (cumulative incidence, 5% [95% CI, 2%-8%]). This included 1 case of CIN-2+ in 44 oncogenic HPV-negative HIV-infected women with CD4 cell count less than 350 cells/μL (cumulative incidence,2% [95% CI, 0%-7%]), 1 case in 47 women with CD4 cell count of 350 to 499 cells/μL (cumulative incidence, 2% [95% CI, 0%-7%]), and 7 cases in 128 women with CD4 cell count of 500 cells/μL or greater (cumulative incidence, 6% [95% CI, 2%-10%]). One HIV-infected and 1 HIV-uninfected woman had CIN-3, but none had cancer. Conclusion: The 5-year cumulative incidence of HSIL+ and CIN-2+ was similar in HIV-infected women and HIV-uninfected women who were cytologically normal and oncogenic HPV-negative at enrollment.
机译:背景:最近修订了针对30岁以上未感染人类免疫缺陷病毒(HIV)的女性的美国子宫颈癌筛查指南,将子宫颈细胞学检查正常的子宫颈癌(Pap)检测间隔从3年提高到5年测试)结果对致癌性人乳头瘤病毒(HPV)的检测结果最阴性。细胞学上正常且致癌性HPV阴性的HIV感染妇女是否可以使用3年或5年的筛查间隔尚不清楚。目的:确定在细胞学上(高度鳞状上皮内病变或更大[HSIL +]或组织学上(宫颈上皮内瘤变2或更大[CIN-2 +])定义为2个独立终点的子宫颈癌前体癌或癌症的风险,在基线时具有正常Pap检测结果且致癌HPV阴性的HIV感染妇女和HIV未感染妇女。设计,设置和参加者:在2001年10月1日至9月30日期间,该研究纳入了多机构美国妇女跨机构艾滋病研究队列,其中包括420例受HIV感染的妇女和279例宫颈细胞学正常的未感染HIV的妇女。 ,2002年进行随访,直至2011年4月30日。每半年在6个临床部位进行随访,包括巴氏涂片检查和宫颈活检。使用聚合酶链反应对入组的宫颈阴道灌洗标本进行HPV DNA测试。初步分析在随访5年时被截断。主要指标:五年前宫颈癌和癌症的累积发病率。结果:369例(88%[95%CI,84%-91%])感染了HIV的女性和255例(91%[95%CI,88%-94%])未感染HIV的女性中未检测到致癌的HPV入学时宫颈细胞学正常。在这些致癌的HPV阴性女性中,观察到2例HSIL +病例。一名未感染HIV的妇女和一名CD4细胞计数为500细胞/μL或更高的HIV感染妇女。从6个临床部位中的4个获得组织学数据。 145例未感染HIV的女性中有6例CIN-2 +(累计发生率,5%[95%CI,1%-8%]),219例HIV感染女性中有9例(累计发生率,5%[95] %CI,2%-8%])。其中包括44例CD4细胞计数低于350细胞/μL的,致癌的HPV阴性HIV感染女性中的CIN-2 + 1例(累积发生率,2%[95%CI,0%-7%]),1例在47名CD4细胞计数为350至499个细胞/μL的女性中(累计发生率,2%[95%CI,0%-7%]),在128名CD4细胞计数为500个细胞/μL或更高的女性中有7例(累计发生率6%[95%CI,2%-10%])。一名感染艾滋病毒的妇女和一名未感染艾滋病毒的妇女患有CIN-3,但无一例患有癌症。结论:HSIL +和CIN-2 +的5年累积发生率在HIV感染妇女和未感染HIV的妇女中,这些妇女在细胞学上正常且致癌的HPV阴性。

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