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乌干达马尤盖区综合宫颈癌筛查(ASPIRE 马尤盖):一项实用的序贯集群随机试验方案。

Integrated cervical cancer screening in Mayuge District Uganda (ASPIRE Mayuge): a pragmatic sequential cluster randomized trial protocol.

机构信息

Uganda Cancer Institute, Kampala, Uganda.

Women's Health Research Institute, Vancouver, Canada.

出版信息

BMC Public Health. 2020 Jan 31;20(1):142. doi: 10.1186/s12889-020-8216-9.

Abstract

BACKGROUND

Cervical cancer is almost entirely preventable through vaccination and screening, yet remains one of the 'gravest threats to women's lives' according to the World Health Organization. Specific high-risk subtypes of human papillomavirus (HR-HPV) are well-established as the primary cause of cervical cancer. Uganda has one of the highest cervical cancer incidence rates in the world (54.8 per 100,000) as a result of limited screening access and infrastructure. The integration of a self-collected cervical cancer screening program using HPV testing within existing community-based primary health care services could increase access to screening and reduce cervical cancer rates among Ugandan women.

METHODS

Using a pragmatic, sequential, cluster randomized trial design; we will compare the effectiveness of two cervical cancer screening models for self-collected HPV testing: 1) community health worker recruitment (door-to-door); and 2) community health meetings. In Mayuge district, Uganda, 31 villages are randomized to one of two treatment arms. Due to the nature of this trial, blinding is not possible. Women are eligible to participate if they have no previous history of hysterectomy or treatment for cervical cancer or pre-cancer and are aged 25-49 years old. All participants receive an integrated package of cervical cancer screening and education. Samples are tested for HPV using GeneXpert point of care testing. All women who test positive for HR-HPV types are referred to a designated health centre for follow-up inspection by Visual Inspection with Acetic acid (VIA) and treatment with thermal ablation. The primary outcome for the trial is the number of women who attend follow-up for VIA screening at a designated Health Centre after a positive HR-HPV test out of all women screened per arm. Secondary outcomes include: cervical cancer screening knowledge; patient-reported experience measures for self-collected cervical cancer screening; and HPV incidence.

DISCUSSION

Results from this study will inform the national scale-up of cervical cancer screening in Uganda, aligning with the World Health Organization's target of achieving cervical cancer elimination through the pillar of increased HPV screening coverage.

TRIAL REGISTRATION

ISRCTN, ISRCTN12767014. Registered 14 May 2019, https://doi.org/10.1186/ISRCTN12767014; clinicaltrials.gov, NCT04000503; Registered 27 June 2019, https://clinicaltrials.gov/ct2/show/NCT04000503 PROTOCOL VERSION: January 8, 2020, version 1.

摘要

背景

宫颈癌几乎可以通过疫苗接种和筛查完全预防,但根据世界卫生组织的说法,它仍然是“对女性生命的最严重威胁之一”。特定的高危型人乳头瘤病毒(HR-HPV)已被确定为宫颈癌的主要病因。由于筛查机会和基础设施有限,乌干达的宫颈癌发病率是世界上最高的之一(每 10 万人中有 54.8 例)。在现有的社区基层医疗保健服务中纳入自我采集的宫颈癌筛查计划,使用 HPV 检测,这可能会增加筛查机会并降低乌干达妇女的宫颈癌发病率。

方法

采用实用的、顺序的、聚类随机试验设计;我们将比较两种用于自我采集 HPV 检测的宫颈癌筛查模型的有效性:1)社区卫生工作者招聘(挨家挨户);2)社区卫生会议。在乌干达马尤盖区,将 31 个村庄随机分配到两个治疗组之一。由于试验的性质,无法进行盲法。如果女性没有子宫切除术或宫颈癌或癌前病变的治疗史,年龄在 25-49 岁之间,则有资格参加。所有参与者都接受了综合的宫颈癌筛查和教育方案。使用 GeneXpert 即时检测对样本进行 HPV 检测。所有 HR-HPV 检测呈阳性的女性都被转介到指定的卫生中心,通过醋酸视觉检查(VIA)和热消融治疗进行随访检查。该试验的主要结局是每臂筛查的所有女性中,在 HR-HPV 检测呈阳性后到指定卫生中心接受 VIA 筛查的女性人数。次要结局包括:宫颈癌筛查知识;自我采集宫颈癌筛查的患者报告体验测量;HPV 发病率。

讨论

该研究的结果将为乌干达全国范围内扩大宫颈癌筛查提供信息,符合世界卫生组织通过增加 HPV 筛查覆盖率来实现宫颈癌消除的目标。

试验注册

ISRCTN,ISRCTN12767014。2019 年 5 月 14 日注册,https://doi.org/10.1186/ISRCTN12767014;clinicaltrials.gov,NCT04000503;2019 年 6 月 27 日注册,https://clinicaltrials.gov/ct2/show/NCT04000503;方案版本:2020 年 1 月 8 日,第 1 版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc39/6995074/2867672235be/12889_2020_8216_Fig1_HTML.jpg

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