Berger Barry M, Parton Marcus A, Levin Bernard
Exact Sciences Corporation, 441 Charmany Dr, Madison, WI 553719. E-mail:
Am J Manag Care. 2016 Feb 1;22(2):e77-81.
The US Preventive Services Task Force (USPSTF) released draft recommendations regarding colorectal cancer (CRC) screening in October 2015. Despite evidence that annual fecal blood testing test use is uncommon in screen eligible adults, with only 10.4% reporting the use of such a test in 2012, and features poor adherence over time, the USPSTF recommended only 3 noninvasive screening strategy options, all including annual fecal occult blood testing: 1) annual fecal immunochemical test (FIT) alone; 2) annual FIT in combination with flexible sigmoidoscopy every 10 years; and 3) annual high-sensitivity fecal occult blood test (hsFOBT). Mt-sDNA is the only FDA-approved CRC screening test, is covered by Medicare every 3 years, and is included as an every-3-year (3y) option in the American Cancer Society guidelines. We demonstrate that USPSTF modeling includes an embedded sensitivity analysis of less frequent than annual test adherence, which provides support for the inclusion of mt-sDNA 3y as a recommended test.
A descriptive analysis of USPSTF modeling of the clinical impact of various stool based CRC screening strategies.
We analyzed the data generated by the USPSTF CRC screening models describing the impact of noninvasive CRC screening strategies on CRC incidence, CRC related mortality, life years gained (LYG), colonoscopy volume and associated complication, test efficiency (a measure of benefits (LYG) and harms (colonoscopies generated), and identified strategies that provide 90% or more of the LYG by screening with colonoscopy every 10 years. We compared mt-sDNA at 3y intervals and FIT and hsFOBT at 2-year (2y) and 3y intervals and did not consider annual testing.
We found that only mt-sDNA 3y, FIT 2y, and FIT 3y were within 98% of the efficiency frontier. However, only mt-sDNA 3y generates more than 90% of the life-years gained with screening colonoscopy. These results meet the USPSTF criteria for a recommendation for mt-sDNA 3y for routine screening.
Given poor adherence to annual testing, any screening opportunity with a test, such as mt-sDNA, that has high sensitivity for CRC and for the most significant precancerous lesions would be an important screening option for patients for maximizing screening effectiveness in reducing CRC incidence and mortality.
美国预防服务工作组(USPSTF)于2015年10月发布了关于结直肠癌(CRC)筛查的建议草案。尽管有证据表明,在适合筛查的成年人中,每年进行粪便潜血检测的情况并不常见,2012年只有10.4%的人报告使用过此类检测,而且随着时间推移其依从性较差,但USPSTF仅推荐了3种非侵入性筛查策略选项,均包括每年进行粪便潜血检测:1)仅每年进行粪便免疫化学检测(FIT);2)每年进行FIT并每10年结合一次乙状结肠镜检查;3)每年进行高灵敏度粪便潜血检测(hsFOBT)。线粒体-sDNA(Mt-sDNA)是唯一经美国食品药品监督管理局(FDA)批准的CRC筛查检测,医疗保险每3年覆盖一次,并且被纳入美国癌症协会指南中的每3年(3y)筛查选项。我们证明,USPSTF的模型包括对低于每年检测依从性的嵌入式敏感性分析,这为将Mt-sDNA每3年检测作为推荐检测提供了支持。
对USPSTF关于各种基于粪便的CRC筛查策略临床影响的模型进行描述性分析。
我们分析了USPSTF CRC筛查模型生成的数据,这些数据描述了非侵入性CRC筛查策略对CRC发病率、CRC相关死亡率、获得的生命年数(LYG)、结肠镜检查量及相关并发症、检测效率(一种衡量益处(LYG)和危害(产生的结肠镜检查量)的指标)的影响,并确定了通过每10年进行一次结肠镜检查筛查可提供90%或更多LYG的策略。我们比较了每3年进行一次的Mt-sDNA以及每2年(2y)和每3年进行一次FIT和hsFOBT的情况,未考虑每年检测的情况。
我们发现,只有每3年进行一次的Mt-sDNA、每2年进行一次的FIT和每3年进行一次的FIT在效率前沿的98%以内。然而,只有每3年进行一次的Mt-sDNA能通过结肠镜检查筛查获得超过90%的生命年数。这些结果符合USPSTF对推荐每3年进行一次Mt-sDNA常规筛查的标准。
鉴于每年检测的依从性较差,对于CRC及最主要癌前病变具有高灵敏度的检测(如Mt-sDNA)的任何筛查机会,都将是患者提高筛查效果以降低CRC发病率和死亡率的重要筛查选项。