Infectious Diseases Division, University Hospital Germans Trias, Barcelona, Spain; Fight Infections Foundation, Barcelona, Spain.
Infectious Diseases Division, University Hospital Germans Trias, Barcelona, Spain; Fight Infections Foundation, Barcelona, Spain.
Lancet HIV. 2024 Sep;11(9):e598-e606. doi: 10.1016/S2352-3018(24)00174-7. Epub 2024 Aug 2.
People with HIV have a substantially higher risk of anal cancer than the general population. We aimed to identify risk factors associated with the development of anal cancer among people with HIV to implement more effective and targeted screening strategies.
We conducted a multicentre retrospective cohort study in 16 hospitals across Catalonia and the Balearic Islands, Spain, between Jan 1, 1998, and Dec 31, 2022. Treatment-naive people with HIV nested in the PISCIS cohort aged 16 years and older with biopsy-proven squamous cell carcinoma of the anus or anal canal were eligible for inclusion. Data were retrieved from every hospital registry and were centrally validated in the PISCIS cohort and the Public Data Analysis for Health Research and Innovation Program. The primary outcome was the incidence rate (IR) of histologically confirmed anal cancer. We used Poisson regression to examine the association between the following risk factors and incidence of anal cancer: age, mode of HIV transmission, nadir CD4 cell count, and time period of HIV diagnosis.
Among 14 238 people with HIV, 107 (0·8%) developed anal cancer, with an overall IR of 72·5 cases per 100 000 person-years (95% CI 59·4-87·6) and median follow-up of 9·5 years (IQR 4·4-15·7). Of these patients with anal cancer, 37 (34·6%) died, of which 24 (64·9%) deaths were related to anal cancer. Incidence was highest among people with HIV with historical nadir CD4 counts of less than 200 cells per μL (IR 105·0 person-years, 95% CI 82·0-132·5) and lowest among those with counts of more than 350 cells per μL (2·9 person-years, 0·1-16·0). Among men who have sex with men (MSM), the IR was 211·5 person-years (95% CI 151·1-211·7) among those with a CD4 count of less than 200 cells per μL, 37·6 person-years (16·2-74·1) among those with a count of 200-350 cells per μL, and 4·8 person-years (0·1-26·9) among those with a count of more than 350 cells per μL. Among people with HIV younger than 30 years, there were no cases of anal cancer among women or men who do not have sex with men, and one case among MSM with a nadir CD4 count of more than 350 cells per μL (IR 4·8 person-years, 95% CI 0·1-26·9). In the multivariable analysis, people with HIV with nadir CD4 counts of more than 350 cells per μL had the lowest risk of developing anal cancer, compared with people with HIV with counts of less than 200 cells per μL (adjusted IR ratio 0·03, 95% CI 0·00-0·25; p=0·0010) or 200-350 cells per μL (0·30, 0·17-0·55; p<0·0001). Compared with people with HIV younger than 30 years, people with HIV aged 60 years and older had an adjusted IR ratio of 27·6 (3·7-206·9; p=0·0010) and people with HIV aged 45-59 years of 21·6 (3·0-156·4; p=0·0020). Compared with individuals diagnosed after 2015, a diagnosis of HIV before 1998 had an adjusted IR ratio of 33·0 (7·9-137·5; p<0·0001).
A nadir CD4 count threshold below 350 cells per μL, particularly less than 200 cells per μL, has the potential to identify people with HIV at heightened risk of developing anal cancer. Customised screening strategies that prioritise screening for individuals at high risk with this surrogate marker could maximise available resources. External validation of these data with other cohorts is required before screening recommendations can be updated.
Catalan Health Department, Generalitat de Catalunya.
与普通人群相比,HIV 感染者罹患肛门癌的风险要高得多。我们旨在确定与 HIV 感染者肛门癌发展相关的风险因素,以便实施更有效和有针对性的筛查策略。
我们在西班牙加泰罗尼亚和巴利阿里群岛的 16 家医院进行了一项多中心回顾性队列研究,时间为 1998 年 1 月 1 日至 2022 年 12 月 31 日。符合条件的患者为年龄在 16 岁及以上、无治疗史且经活检证实为肛门或肛管鳞癌的 HIV 感染者。数据来自每个医院的登记处,并在 PISCIS 队列和公共数据分析用于健康研究和创新计划中进行了集中验证。主要结局是经组织学证实的肛门癌的发病率(IR)。我们使用泊松回归分析了以下风险因素与肛门癌发病之间的关系:年龄、HIV 传播模式、最低 CD4 细胞计数和 HIV 诊断时间区间。
在 14238 名 HIV 感染者中,有 107 人(0.8%)罹患肛门癌,总发病率为 72.5/10 万患者年(95%CI 59.4-87.6),中位随访时间为 9.5 年(IQR 4.4-15.7)。在这些肛门癌患者中,有 37 人(34.6%)死亡,其中 24 人(64.9%)的死亡与肛门癌相关。发病率在 HIV 感染者中最高,历史最低 CD4 计数<200 个/μL 的发病率为 105.0/10 万患者年(95%CI 82.0-132.5),而最低 CD4 计数>350 个/μL 的发病率为 2.9/10 万患者年(0.1-16.0)。在男男性行为者(MSM)中,CD4 计数<200 个/μL 的 MSM 发病率为 211.5/10 万患者年(95%CI 151.1-211.7),200-350 个/μL 的为 37.6/10 万患者年(16.2-74.1),>350 个/μL 的为 4.8/10 万患者年(0.1-26.9)。在年龄<30 岁的 HIV 感染者中,无性行为的女性或男性均未发生肛门癌,而 HIV 感染者中仅有 1 例 MSM 发生肛门癌,且该例患者的 CD4 计数>350 个/μL(IR 4.8/10 万患者年,95%CI 0.1-26.9)。在多变量分析中,与 CD4 计数<200 个/μL 或 200-350 个/μL 的 HIV 感染者相比,CD4 计数>350 个/μL 的 HIV 感染者罹患肛门癌的风险最低(调整后的 IR 比值分别为 0.03,95%CI 0.00-0.25;p=0.0010 和 0.30,95%CI 0.17-0.55;p<0.0001)。与年龄<30 岁的 HIV 感染者相比,年龄在 60 岁及以上的 HIV 感染者调整后的 IR 比值为 27.6(95%CI 3.7-206.9;p=0.0010),年龄在 45-59 岁的 HIV 感染者为 21.6(95%CI 3.0-156.4;p=0.0020)。与在 2015 年后诊断的患者相比,1998 年前诊断的 HIV 患者的调整后的 IR 比值为 33.0(7.9-137.5;p<0.0001)。
CD4 细胞计数的最低值<350 个/μL,特别是<200 个/μL,可能是识别具有罹患肛门癌高风险的 HIV 感染者的一个潜在指标。使用该替代标志物对具有此类高风险的人群进行有针对性的筛查,可以最大限度地利用现有资源。在更新筛查建议之前,需要对其他队列的数据进行外部验证。
加泰罗尼亚卫生部,加泰罗尼亚自治区。