Haug Ulrike, Knudsen Amy B, Lansdorp-Vogelaar Iris, Kuntz Karen M
Epidemiological Cancer Registry Baden-Wuerttemberg, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Int J Cancer. 2015 Jun 15;136(12):2864-74. doi: 10.1002/ijc.29343. Epub 2014 Dec 3.
Researchers are actively pursuing the development of a new non-invasive test (NIT) for colorectal cancer (CRC) screening as an alternative to fecal occult blood tests (FOBTs). The majority of pilot studies focus on the detection of invasive CRC rather than precursor lesions (i.e., adenomas). We aimed to explore the relevance of adenoma detection for the viability of an NIT for CRC screening by considering a hypothetical test that does not detect adenomas beyond chance. We used the Simulation Model of Colorectal Cancer (SimCRC) to estimate the effectiveness of CRC screening and the lifetime costs (payers' perspective) for a cohort of US 50-years-old persons to whom CRC screening is offered from age 50-75. We compared annual screening with guaiac and immunochemical FOBTs (with sensitivities up to 70 and 24% for CRC and adenomas, respectively) to annual screening with a hypothetical NIT (sensitivity of 90% for CRC, no detection of adenomas beyond chance, specificity and cost similar to FOBTs). Screening with the NIT was not more effective, but was 29-44% more costly than screening with FOBTs. The findings were robust to varying the screening interval, the NIT's sensitivity for CRC, adherence rates favoring the NIT, and the NIT's unit cost. A comparative modelling approach using a model that assumes a shorter adenoma dwell time (MISCAN-COLON) confirmed the superiority of the immunochemical FOBT over an NIT with no ability to detect adenomas. Information on adenoma detection is crucial to determine whether a new NIT is a viable alternative to FOBTs for CRC screening. Current evidence thus lacks an important piece of information to identify marker candidates that hold real promise and deserve further (large-scale) evaluation.
研究人员正在积极致力于开发一种用于结直肠癌(CRC)筛查的新型非侵入性检测方法(NIT),以替代粪便潜血检测(FOBT)。大多数试点研究聚焦于侵袭性CRC的检测,而非前驱病变(即腺瘤)。我们旨在通过考虑一种除偶然情况外无法检测腺瘤的假设检测方法,探讨腺瘤检测对于CRC筛查NIT可行性的相关性。我们使用结直肠癌模拟模型(SimCRC)来估计CRC筛查的有效性以及从50岁至75岁接受CRC筛查的美国50岁人群队列的终生成本(从支付方角度)。我们将每年使用愈创木脂法和免疫化学法FOBT进行筛查(对CRC和腺瘤的敏感性分别高达70%和24%)与每年使用假设的NIT进行筛查(对CRC的敏感性为90%,除偶然情况外无法检测腺瘤,特异性和成本与FOBT相似)进行了比较。使用NIT进行筛查并不更有效,但成本比使用FOBT筛查高出29% - 44%。这些发现对于改变筛查间隔、NIT对CRC的敏感性、有利于NIT的依从率以及NIT的单位成本具有稳健性。使用假设腺瘤停留时间较短的模型(MISCAN - COLON)进行的比较建模方法证实了免疫化学FOBT优于无法检测腺瘤的NIT。关于腺瘤检测的信息对于确定一种新的NIT是否是CRC筛查中FOBT的可行替代方法至关重要。因此,目前的证据缺乏识别真正有前景且值得进一步(大规模)评估的标志物候选物所需的一项重要信息。