Westwood Marie, Corro Ramos Isaac, Lang Shona, Luyendijk Marianne, Zaim Remziye, Stirk Lisa, Al Maiwenn, Armstrong Nigel, Kleijnen Jos
Kleijnen Systematic Reviews Ltd, York, UK.
Institute for Medical Technology Assessment, Erasmus University Rotterdam, Rotterdam, the Netherlands.
Health Technol Assess. 2017 May;21(33):1-234. doi: 10.3310/hta21330.
Colorectal cancer (CRC) is the third most common cancer in the UK. Presenting symptoms that can be associated with CRC usually have another explanation. Faecal immunochemical tests (FITs) detect blood that is not visible to the naked eye and may help to select patients who are likely to benefit from further investigation.
To assess the effectiveness of FITs [OC-Sensor (Eiken Chemical Co./MAST Diagnostics, Tokyo, Japan), HM-JACKarc (Kyowa Medex/Alpha Laboratories Ltd, Tokyo, Japan), FOB Gold (Sentinel/Sysmex, Sentinel Diagnostics, Milan, Italy), RIDASCREEN Hb or RIDASCREEN Hb/Hp complex (R-Biopharm, Darmstadt, Germany)] for primary care triage of people with low-risk symptoms.
Twenty-four resources were searched to March 2016. Review methods followed published guidelines. Summary estimates were calculated using a bivariate model or a random-effects logistic regression model. The cost-effectiveness analysis considered long-term costs and quality-adjusted life-years (QALYs) that were associated with different faecal occult blood tests and direct colonoscopy referral. Modelling comprised a diagnostic decision model, a Markov model for long-term costs and QALYs that were associated with CRC treatment and progression, and a Markov model for QALYs that were associated with no CRC.
We included 10 studies. Using a single sample and 10 µg Hb/g faeces threshold, sensitivity estimates for OC-Sensor [92.1%, 95% confidence interval (CI) 86.9% to 95.3%] and HM-JACKarc (100%, 95% CI 71.5% to 100%) indicated that both may be useful to rule out CRC. Specificity estimates were 85.8% (95% CI 78.3% to 91.0%) and 76.6% (95% CI 72.6% to 80.3%). Triage using FITs could rule out CRC and avoid colonoscopy in approximately 75% of symptomatic patients. Data from our systematic review suggest that 22.5-93% of patients with a positive FIT and no CRC have other significant bowel pathologies. The results of the base-case analysis suggested minimal difference in QALYs between all of the strategies; no triage (referral straight to colonoscopy) is the most expensive. Faecal immunochemical testing was cost-effective (cheaper and more, or only slightly less, effective) compared with no triage. Faecal immunochemical testing was more effective and costly than guaiac faecal occult blood testing, but remained cost-effective at a threshold incremental cost-effectiveness ratio of £30,000. The results of scenario analyses did not differ substantively from the base-case. Results were better for faecal immunochemical testing when accuracy of the guaiac faecal occult blood test (gFOBT) was based on studies that were more representative of the correct population.
Only one included study evaluated faecal immunochemical testing in primary care; however, all of the other studies evaluated faecal immunochemical testing at the point of referral. Further, validation data for the Faecal haemoglobin, Age and Sex Test (FAST) score, which includes faecal immunochemical testing, showed no significant difference in performance between primary and secondary care. There were insufficient data to adequately assess FOB Gold, RIDASCREEN Hb or RIDASCREEN Hb/Hp complex. No study compared FIT assays, or FIT assays versus gFOBT; all of the data included in this assessment refer to the clinical effectiveness of individual FIT methods and their comparative effectiveness.
Faecal immunochemical testing is likely to be a clinically effective and cost-effective strategy for triaging people who are presenting, in primary care settings, with lower abdominal symptoms and who are at low risk for CRC. Further research is required to confirm the effectiveness of faecal immunochemical testing in primary care practice and to compare the performance of different FIT assays.
This study is registered as PROSPERO CRD42016037723.
The National Institute for Health Research Health Technology Assessment programme.
结直肠癌(CRC)是英国第三大常见癌症。与CRC相关的症状通常另有原因。粪便免疫化学检测(FIT)可检测肉眼不可见的血液,可能有助于筛选出可能从进一步检查中获益的患者。
评估FIT [OC-Sensor(日本东京荣研化学株式会社/MAST诊断公司)、HM-JACKarc(日本东京协和梅迪克/Alpha实验室有限公司)、FOB Gold(意大利米兰哨兵诊断公司/Sysmex公司)、RIDASCREEN Hb或RIDASCREEN Hb/Hp复合物(德国达姆施塔特R-Biopharm公司)] 用于初级保健中对低风险症状人群进行分诊的有效性。
截至2016年3月检索了24种资源。综述方法遵循已发表的指南。使用双变量模型或随机效应逻辑回归模型计算汇总估计值。成本效益分析考虑了与不同粪便潜血检测和直接结肠镜检查转诊相关的长期成本和质量调整生命年(QALY)。建模包括一个诊断决策模型、一个与CRC治疗和进展相关的长期成本和QALY的马尔可夫模型,以及一个与无CRC相关的QALY的马尔可夫模型。
我们纳入了10项研究。使用单个样本和10 μg Hb/g粪便阈值,OC-Sensor的敏感性估计值为92.1% [95%置信区间(CI)86.9%至95.3%],HM-JACKarc为(100%,95% CI 71.5%至100%),表明两者可能都有助于排除CRC。特异性估计值分别为85.8%(95% CI 78.3%至91.0%)和76.6%(95% CI 72.6%至80.3%)。使用FIT进行分诊可在约75%有症状的患者中排除CRC并避免结肠镜检查。我们系统评价的数据表明,FIT结果阳性且无CRC的患者中有22.5% - 93%存在其他严重肠道病变。基础病例分析结果表明,所有策略之间的QALY差异极小;不进行分诊(直接转诊至结肠镜检查)成本最高。与不进行分诊相比,粪便免疫化学检测具有成本效益(更便宜且效果相当或仅略差)。粪便免疫化学检测比愈创木脂粪便潜血检测更有效且成本更高,但在阈值增量成本效益比为30,000英镑时仍具有成本效益。情景分析结果与基础病例分析没有实质性差异。当愈创木脂粪便潜血检测(gFOBT)的准确性基于更能代表正确人群的研究时,粪便免疫化学检测的结果更好。
纳入的研究中只有一项评估了初级保健中的粪便免疫化学检测;然而,所有其他研究均在转诊时评估了粪便免疫化学检测。此外,包括粪便免疫化学检测的粪便血红蛋白、年龄和性别检测(FAST)评分的验证数据显示,初级保健和二级保健之间的性能无显著差异。评估FOB Gold、RIDASCREEN Hb或RIDASCREEN Hb/Hp复合物的数据不足。没有研究比较FIT检测方法,或FIT检测方法与gFOBT;本评估中纳入的所有数据均指单个FIT方法的临床有效性及其比较有效性。
粪便免疫化学检测可能是一种临床有效且具有成本效益的策略,用于对初级保健环境中出现下腹部症状且患CRC风险较低的人群进行分诊。需要进一步研究以确认粪便免疫化学检测在初级保健实践中的有效性,并比较不同FIT检测方法的性能。
本研究注册为PROSPERO CRD42016037723。
英国国家卫生研究院卫生技术评估计划。