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用于指导初级保健中结直肠癌转诊路径的定量粪便免疫化学检测。一项系统评价、荟萃分析和成本效益分析。

Quantitative faecal immunochemical tests to guide colorectal cancer pathway referral in primary care. A systematic review, meta-analysis and cost-effectiveness analysis.

作者信息

Harnan Sue, Navega Biz Aline, Hamilton Jean, Whyte Sophie, Simpson Emma, Ren Shijie, Cooper Katy, Clowes Mark, Abulafi Muti, Ball Alex, Benton Sally C, Booth Richard, Carten Rachel, Edgar Stephanie, Hamilton Willie, Kurien Matt, Merriman Louise, Monahan Kevin, Heathcote Laura, Stevenson Matt

机构信息

Sheffield Centre for Health and Related Research (SCHARR), School of Medicine and Population Health, University of Sheffield, Sheffield, UK.

Croydon Health Services NHS Trust, London, UK.

出版信息

Health Technol Assess. 2025 Sep;29(46):1-210. doi: 10.3310/AHPE4211.

DOI:10.3310/AHPE4211
PMID:41014070
Abstract

BACKGROUND

Faecal immunochemical tests may be better than symptoms alone at identifying which patients who present to primary care with symptoms are at high risk of colorectal cancer and should have a colonoscopy. This could reduce waiting lists and patient anxiety/discomfort and enable earlier treatment of colorectal cancer. The threshold used will affect how well faecal immunochemical tests work, with a higher threshold resulting in fewer referrals but a greater chance of missing disease.

OBJECTIVE

What is the most clinically effective and cost-effective way to use faecal immunochemical tests to reduce the number of people without significant bowel pathology who are referred to the suspected cancer pathway for colorectal cancer, taking into consideration potential colonoscopy capacity constraints for urgent and non-urgent referrals? Tests were HM-JACKarc, OC-Sensor, FOB Gold, NS-Prime, QuikRead go, IDK TurbiFIT, IDK Hb, IDK Hb/Hp complex and IDKHb+Hb/Hp ELISAs.

DESIGN

Systematic review, meta-analysis and cost-effectiveness analyses were conducted.

REVIEW METHODS

Searches across four databases and six registries were conducted (December 2022). Diagnostic accuracy studies conducted in patients presenting to or referred from primary care with symptoms suggestive of colorectal cancer using any reference standard were included. Risk of bias was assessed with quality assessment of diagnostic test accuracy studies version 2. For each test, sensitivity and specificity were pooled at all reported thresholds and summary estimates were provided at all possible thresholds within the observed range. Comparative accuracy between tests was considered. Other outcomes, for example test uptake, failure and patient acceptability, were also extracted.

COST-EFFECTIVENESS ANALYSIS METHODS: A mathematical model was developed to compare three different diagnostic strategies that used quantitative faecal immunochemical tests in primary care patients with symptoms of colorectal cancer to determine subsequent management pathways. The model assessed the health outcomes and costs associated with each strategy over a lifetime horizon from the perspective of the United Kingdom National Health Service and Personal Social Services, using evidence from published literature and other sources.

RESULTS

Syntheses of sensitivity and specificity were conducted for HM-JACKarc ( = 16 studies), OC-Sensor ( = 11 studies) and FOB Gold ( = 3 studies). No synthesis was conducted for QuikRead go, NS-Prime IDK Hb or IDK Hb/Hp as there was only one study for each. No eligible studies were found for IDK Hb+Hb/Hp or for IDK TurbiFIT. Other outcomes (e.g. patient acceptability) were also synthesised. Model results suggest that faecal immunochemical tests generate a positive incremental net monetary benefit compared with current care, typically in the range of £200-350 per patient, regardless of the threshold used, for the majority of faecal immunochemical tests strategies assessed. These conclusions were robust to the sensitivity analyses undertaken.

CONCLUSIONS

For all faecal immunochemical test brands, there are strategies at which the incremental net monetary benefit is positive compared with current care. The exact brand and threshold(s) that generate the greatest incremental net monetary benefit could not be robustly determined due to the similarity of incremental net monetary benefit values, parameter uncertainty and the possibility of omissions from the model structure.

FUTURE WORK

More data are needed on comparative diagnostic test accuracy and whether different thresholds should be used in some patients (e.g. anaemic, male/female, younger/older).

STUDY REGISTRATION

This study is registered as PROSPERO CRD42022383580.

FUNDING

This award was funded by the National Institute for Health and Care Research (NIHR) Evidence Synthesis programme (NIHR award ref: NIHR135637) and is published in full in Health Technology Assessment; Vol. 29, No. 46. See the NIHR Funding and Awards website for further award information.

摘要

背景

在识别哪些因出现症状而就诊于基层医疗的患者有患结直肠癌的高风险且应接受结肠镜检查方面,粪便免疫化学检测可能比单纯依靠症状更有效。这可以减少候诊名单以及患者的焦虑/不适,并使结直肠癌能更早得到治疗。所采用的阈值会影响粪便免疫化学检测的效果,阈值越高,转诊人数越少,但漏诊疾病的可能性越大。

目的

考虑到紧急和非紧急转诊的潜在结肠镜检查能力限制,使用粪便免疫化学检测以减少被转诊至结直肠癌疑似癌症路径但无明显肠道病变的人数的最具临床效果和成本效益的方法是什么?检测方法包括HM-JACKarc、OC-Sensor、FOB Gold、NS-Prime、QuikRead go、IDK TurbiFIT、IDK Hb、IDK Hb/Hp复合物以及IDKHb+Hb/Hp酶联免疫吸附测定法。

设计

进行了系统评价、荟萃分析和成本效益分析。

综述方法

(于2022年12月)对四个数据库和六个登记处进行了检索。纳入了使用任何参考标准对因出现提示结直肠癌症状而就诊于基层医疗或从基层医疗转诊的患者进行的诊断准确性研究。使用诊断试验准确性研究质量评估第2版对偏倚风险进行评估。对于每项检测,在所有报告的阈值下汇总敏感性和特异性,并在观察范围内的所有可能阈值下提供汇总估计值。考虑了不同检测之间的比较准确性。还提取了其他结果,例如检测接受率、失败率和患者可接受性。

成本效益分析方法

建立了一个数学模型,以比较三种不同的诊断策略,这些策略在患有结直肠癌症状的基层医疗患者中使用定量粪便免疫化学检测来确定后续管理路径。该模型从英国国家医疗服务体系和个人社会服务的角度,利用已发表文献和其他来源的证据,评估了每种策略在整个生命周期内的健康结果和成本。

结果

对HM-JACKarc(n = 16项研究)、OC-Sensor(n = 11项研究)和FOB Gold(n = 3项研究)进行了敏感性和特异性的综合分析。由于QuikRead go、NS-Prime、IDK Hb或IDK Hb/Hp每种仅有一项研究,因此未进行综合分析。未找到关于IDK Hb+Hb/Hp或IDK TurbiFIT的符合条件的研究。还综合了其他结果(例如患者可接受性)。模型结果表明,与当前护理相比,粪便免疫化学检测产生了正的增量净货币效益,对于大多数评估的粪便免疫化学检测策略,通常每位患者在200 - 350英镑范围内,无论使用何种阈值。这些结论对所进行的敏感性分析具有稳健性。

结论

对于所有粪便免疫化学检测品牌,都存在与当前护理相比增量净货币效益为正的策略。由于增量净货币效益值的相似性、参数不确定性以及模型结构可能存在遗漏,无法可靠地确定产生最大增量净货币效益的确切品牌和阈值。

未来工作

需要更多关于比较诊断试验准确性以及某些患者(例如贫血患者、男性/女性、年轻/年长患者)是否应使用不同阈值的数据。

研究注册

本研究已注册为PROSPERO CRD42022383580。

资助

本研究由英国国家卫生与保健研究机构(NIHR)证据综合计划资助(NIHR资助编号:NIHR135637),并全文发表于《卫生技术评估》;第29卷,第46期。有关进一步的资助信息,请参阅NIHR资助与奖项网站。

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