Gottschlich Anna, Gondara Lovedeep, Smith Laurie W, Anderson Jennifer Joy, Cook Darrel, Krajden Mel, Lee Marette, Martin Ruth Elwood, Melnikow Joy, Peacock Stuart, Proctor Lily, Stuart Gavin, Franco Eduardo L, van Niekerk Dirk, Ogilvie Gina S
Women's Health Research Institute, BC Women's Hospital and Health Service, Vancouver, BC, Canada.
Wayne State University, School of Medicine Departments of Oncology, Detroit, MI, USA.
Lancet Reg Health Am. 2023 Sep 29;26:100598. doi: 10.1016/j.lana.2023.100598. eCollection 2023 Oct.
Shifting from cytology to human papillomavirus (HPV)-based cervical cancer screening will initially increase colposcopy referrals. The anticipated impact on health systems has been raised as a concern for implementation. It is unclear if the higher rate of colposcopy referrals is sustained after initial HPV-based screens or reverts to new lower baselines due to earlier detection and treatment of precancer. This study aimed to investigate long-term rates of colposcopy referrals after participation in HPV-based screening.
Participants of HPV for Cervical Cancer Screening trial (HPV FOCAL) received one (HPV1, N = 6204) or two (HPV2, N = 9540) HPV-based screens. After exit, they returned to British Columbia's (BC) cytology screening program. A comparison cohort from the BC screening population (BCS, N = 1,140,745) was identified, mirroring trial inclusion criteria. All participants were followed for 10-14 years through the provincial screening registry. Colposcopy referral rates per 1000 screens were calculated for each group. Trial colposcopy referrals for HPV1 and HPV2 were calculated under two referral scenarios: (1) all HPV positive referred to colposcopy; (2) cytology triage with ASCUS or greater referred to colposcopy. Colposcopy referrals from post-trial screens in HPV1 an HPV2 and all screens in BCS were based on actual recommendations from the screening program. A multivariable flexible survival regression model compared hazard ratios (HR) throughout follow-up.
Scenario 2 referral rates were higher during initial HPV screen(s) vs cytology screen (HPV1: 28 per 1000 screens (95% CI: 24, 33), HPV2: 32 per 1000 screens (95% CI: 29, 36), BCS: 8 per 1000 screens (95% CI: 8.9)). However, post-trial rates in HPV1 and HPV2 were significantly lower than in BCS. Cumulative rates in HPV1 and HPV2 approached the cumulative rate in BCS 11-12 years after HPV-based screening (HPV1: 11 per 1000 screens (95% CI: 10, 12), HPV2: 16 per 1000 screens (95% CI: 15-17), BCS: 11 per 1000 screens (95% CI: 10, 11)). Adjusted models demonstrated reductions in referral rates in HPV1 (HR = 0.6, 95% CI: 0.5, 0.7) and HPV2 (HR = 0.7, 95% CI: 0.6, 0.8) relative to BCS by 54 and 72 months post-final HPV screen respectively.
Reduced colposcopy referral rates were observed after initial rounds of HPV-based screening. After initial HPV screening, referral rates to colposcopy after cytology triage were below the current rates seen in a centralized cytology program after approximately four years. Any expected increase in referrals at initiation of HPV-based screening could be countered by staged program implementation.
This work was supported by the National Institutes of Health (R01 CA221918), Michael Smith Health Research BC (RT-2021-1595), and the Canadian Institutes of Health Research (MCT82072).
从细胞学筛查转向基于人乳头瘤病毒(HPV)的宫颈癌筛查,最初会增加阴道镜检查转诊人数。对卫生系统的预期影响已成为实施过程中的一个关注点。目前尚不清楚在最初基于HPV的筛查后,阴道镜检查转诊率是否会持续升高,还是会因癌前病变的早期检测和治疗而恢复到新的较低基线水平。本研究旨在调查参与基于HPV的筛查后阴道镜检查转诊的长期发生率。
宫颈癌筛查HPV试验(HPV FOCAL)的参与者接受了一次(HPV1组,N = 6204)或两次(HPV2组,N = 9540)基于HPV的筛查。退出试验后,他们回到不列颠哥伦比亚省(BC)的细胞学筛查项目。从BC筛查人群(BCS,N = 1,140,745)中确定了一个对照队列,该队列符合试验纳入标准。通过省级筛查登记处对所有参与者进行了10 - 14年的随访。计算了每组每1000次筛查的阴道镜检查转诊率。HPV1组和HPV2组的试验阴道镜检查转诊率在两种转诊情况下进行计算:(1)所有HPV阳性者转诊至阴道镜检查;(2)对非典型鳞状细胞(ASCUS)及以上的细胞学结果进行分流后转诊至阴道镜检查。HPV1组和HPV2组试验后筛查的阴道镜检查转诊以及BCS组所有筛查的阴道镜检查转诊均基于筛查项目的实际建议。采用多变量灵活生存回归模型比较了整个随访期间的风险比(HR)。
在最初的HPV筛查期间,情况2的转诊率高于细胞学筛查(HPV1组:每1000次筛查28例(95%CI:24,33),HPV2组:每1000次筛查32例(95%CI:29,36),BCS组:每1000次筛查8例(95%CI:8.9))。然而,HPV1组和HPV2组试验后的转诊率显著低于BCS组。HPV1组和HPV2组的累积转诊率在基于HPV的筛查后11 - 12年接近BCS组的累积转诊率(HPV1组:每1000次筛查11例(95%CI:10,12),HPV2组:每1000次筛查16例(95%CI:15 - 17),BCS组:每1000次筛查11例(95%CI:10,11))。调整后的模型显示,相对于BCS组,HPV1组(HR = 0.6,95%CI:0.5,0.7)和HPV2组(HR = 0.7,95%CI:0.6,0.8)在最后一次HPV筛查后分别在54个月和72个月时转诊率降低。
在首轮基于HPV的筛查后,观察到阴道镜检查转诊率降低。在最初的HPV筛查后,经过细胞学分流后的阴道镜检查转诊率在大约四年后低于目前集中式细胞学项目中的转诊率。基于HPV的筛查开始时预期的转诊增加可通过分阶段实施项目来抵消。
本研究得到了美国国立卫生研究院(R01 CA221918)、不列颠哥伦比亚省迈克尔·史密斯健康研究基金会(RT - 2021 - 1595)以及加拿大卫生研究院(MCT82072)的支持。