Department of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Botswana Harvard Health Partnership, Gaborone, Botswana.
BMJ Open. 2024 Oct 29;14(10):e089375. doi: 10.1136/bmjopen-2024-089375.
International guidelines recommend cervical screening cessation at age 50 following two consecutive negative screens. However, many women aged 50 and older in low-income and middle-income countries (LMICs) have not had prior opportunity to screen. We examine the prevalence of cervical dysplasia and cervical cancer stage in Botswana women aged 50+ compared with 30-49, stratified by HIV status.
Secondary analysis of data from two prospective cohort studies.
The screening cohort was recruited at health facilities in South East District. The cancer cohort was recruited from the primary public tertiary referral hospital and a private hospital in Gaborone, Botswana.
The screening cohort included 2570 women aged 30 and older recruited from February 2021 to August 2022. Screening eligibility included anyone with a cervix and without a prior history of cervical cancer. The cancer cohort included 1520 patients diagnosed with cervical cancer who sought care at the facilities where recruitment took place from January 2015 to December 2022.
The prevalence of cervical intraepithelial neoplasia (CIN)2+ and cancer stage at diagnosis was compared across age groups, stratified by HIV status. Prevalence ratios were calculated for the association between age and CIN2+/CIN3+via log-binomial regression.
The prevalence of CIN2+ was similar between 30-49 years old and 50+, both among women with HIV (WWH, 15.9% and 19.3%, respectively) and without HIV (13.3% and 10.4%, respectively). Similar findings were found when CIN3+ was used as the outcome. There were no statistically significant differences in prevalence ratios (PRs) across age groups for CIN2+ (adjusted PR (aPR) WWH 1.1 (95% CI 0.80 to 1.6); aPR HIV- 0.78 (95% CI 0.45 to 1.4) nor CIN3+ (aPR WWH 1.1 (95% CI 0.70 to 1.6); aPR HIV- 0.81 (95% CI 0.40 to 1.7)). Nearly half of cervical cancer diagnoses were made in women 50+; three-quarters of cases in women without HIV were diagnosed at 50+ years.
Our findings demonstrate the prevalence of high-grade cervical dysplasia and cervical cancer remains high beyond age 50 in both women with and without HIV in an LMIC context with high HIV prevalence. Screening women 50+ will allow treatment for cervical dysplasia and may provide early diagnosis of curable cervical cancer. These findings support the rapid introduction of high-performance cervical screening to increase access for women 50+.
NCT04242823.
国际指南建议在连续两次阴性筛查后,年龄为 50 岁的女性停止宫颈筛查。然而,许多低收入和中等收入国家(LMIC)的 50 岁及以上女性以前没有机会进行筛查。我们研究了博茨瓦纳年龄在 50 岁及以上的女性与 30-49 岁的女性相比,在 HIV 阳性和阴性的情况下,宫颈发育不良和宫颈癌分期的流行率。
对来自两项前瞻性队列研究的数据进行二次分析。
筛查队列是在东南区的卫生机构招募的。癌症队列是从博茨瓦纳哈博罗内的一家初级公立三级转诊医院和一家私立医院招募的。
筛查队列包括 2570 名年龄在 30 岁及以上的女性,招募时间为 2021 年 2 月至 2022 年 8 月。筛查合格者包括有子宫颈且无宫颈癌病史的任何人。癌症队列包括在招募地点的医疗机构就诊的 1520 名宫颈癌患者,从 2015 年 1 月至 2022 年 12 月期间。
比较了不同年龄组中 HIV 阳性(WWH)和 HIV 阴性(HIV-)妇女中宫颈上皮内瘤变(CIN)2+和癌症诊断期的流行率。使用对数二项回归计算年龄与 CIN2+/CIN3+之间的关联的优势比(PR)。
在 HIV 阳性(WWH)和 HIV 阴性(HIV-)的女性中,30-49 岁和 50 岁及以上的 CIN2+的流行率相似(分别为 15.9%和 19.3%)。当使用 CIN3+作为结局时,也发现了相似的结果。在 CIN2+(调整后优势比(aPR)WWH 1.1(95%置信区间 0.80 至 1.6);aPR HIV-0.78(95%置信区间 0.45 至 1.4)和 CIN3+(aPR WWH 1.1(95%置信区间 0.70 至 1.6);aPR HIV-0.81(95%置信区间 0.40 至 1.7))方面,年龄组之间没有统计学意义的 PR 差异。几乎一半的宫颈癌诊断发生在 50 岁以上的女性;四分之三的无 HIV 女性病例在 50 岁及以上被诊断。
我们的研究结果表明,在 HIV 患病率较高的 LMIC 环境中,无论是 HIV 阳性还是阴性的女性,50 岁以上的女性中高度宫颈发育不良和宫颈癌的患病率仍然很高。对 50 岁以上的女性进行筛查将有助于治疗宫颈发育不良,并可能有助于早期诊断可治愈的宫颈癌。这些发现支持快速引入高性能宫颈筛查,以增加 50 岁以上女性的机会。
NCT04242823。