Harlass Matthias, Dalmat Ronit R, Chubak Jessica, van den Puttelaar Rosita, Udaltsova Natalia, Corley Douglas A, Jensen Christopher D, Collier Nicholson, Ozik Jonathan, Lansdorp-Vogelaar Iris, Meester Reinier G S
Department of Public Health, Erasmus University Medical Center, Rotterdam, South Holland, the Netherlands.
Department of Global Health, University of Washington, Seattle.
JAMA Netw Open. 2024 Dec 2;7(12):e2451715. doi: 10.1001/jamanetworkopen.2024.51715.
Prior studies have shown that the benefits, harms, and costs of colorectal cancer (CRC) screening at older ages are associated with a patient's sex, health, and screening history. However, these studies were hypothetical exercises and not directly informed by data on CRC risk.
To identify the optimal stopping ages for CRC screening by sex, comorbidity, and screening history from a cost-effectiveness perspective.
DESIGN, SETTING, AND PARTICIPANTS: This economic evaluation first validated the MISCAN-Colon (Microsimulation Screening Analysis-Colon) model against community-based CRC incidence and mortality rates for 2 subcohorts of the PRECISE (Optimizing Colorectal Cancer Screening Precision and Outcomes in Community-Based Populations) cohort. Subsequently, different CRC screening scenarios were simulated in older individuals. Cohorts of US adults aged 76 to 90 years varied by sex and comorbidity status (none, low, moderate, or severe). Statistical and sensitivity analyses were performed from March 2023 to May 2024.
CRC screening histories including fecal immunochemical test (FIT) or colonoscopy, such as a negative colonoscopy result from 10, 15, 20, 25, or 30 years before the index age; 1 to 5 negative FIT results within 5 years of the index age, with different patterns of recency; or a combination of negative colonoscopy and negative FIT results.
The main outcomes included estimated lifetime clinical outcomes, incremental costs, and quality-adjusted life-years gained (QALYG) associated with 1 additional FIT or colonoscopy. Optimal stopping age for screening, defined as the oldest age for which the incremental cost-effectiveness ratio was still below the willingness-to-pay threshold of $100 000 per QALYG, was evaluated.
The first of the 2 PRECISE subcohorts used in validating the simulation model included 25 974 adults (15 060 females [58.0%]; 54.7% aged 76 to 80 years) with a negative colonoscopy result 10 years before the index date. The second subcohort consisted of 118 269 adults (67 058 females [56.7%]; 90.5% aged 76 to 80 years) with a negative FIT result 1 year before the index date. Older age, male sex, higher comorbidity levels, and recent CRC screenings were associated with reduced incremental benefit and cost-effectiveness of additional screening. For the reference cohort of 76-year-old females without comorbidities and a negative colonoscopy result 10 years before the index age, 1 additional colonoscopy cost $38 226 per QALYG. For cohorts with otherwise equivalent characteristics, associated costs increased to $1 689 945 per QALYG for females at age 90 years without comorbidities and a negative colonoscopy results 10 years before the index age, $51 604 per QALYG for males at age 76 years without comorbidities and a negative colonoscopy result 10 years before the index age, and $108 480 per QALYG for females at age 76 years with severe comorbidities and a negative colonoscopy result 10 years before the index age and decreased to $16 870 per QALYG for females without comorbidities and a negative colonoscopy result 30 years before the index age. The optimal stopping ages across different cohorts ranged from younger than 76 to 86 years for colonoscopy and younger than 76 to 88 years for FIT.
In this economic evaluation, age, sex, screening history, comorbidity, and future screening modality were associated with the clinical outcomes, cost-effectiveness, and optimal stopping age for CRC screening. These results can inform guideline development and patient-directed informed decision-making.
先前的研究表明,老年人大肠癌(CRC)筛查的益处、危害和成本与患者的性别、健康状况和筛查史有关。然而,这些研究是假设性的,并非直接基于CRC风险数据。
从成本效益的角度确定按性别、合并症和筛查史划分的CRC筛查的最佳停止年龄。
设计、设置和参与者:这项经济评估首先针对PRECISE(优化社区人群中的结直肠癌筛查精度和结果)队列的2个亚队列,根据社区CRC发病率和死亡率验证了MISCAN-Colon(微模拟筛查分析-结肠)模型。随后,在老年人中模拟了不同的CRC筛查方案。美国76至90岁成年人队列按性别和合并症状态(无、低、中或重度)划分。2023年3月至2024年5月进行了统计和敏感性分析。
CRC筛查史,包括粪便免疫化学检测(FIT)或结肠镜检查,例如在索引年龄前10、15、20、25或30年结肠镜检查结果为阴性;在索引年龄前5年内有1至5次FIT结果为阴性,且有不同的近期模式;或结肠镜检查阴性和FIT结果阴性的组合。
主要结局包括估计的终生临床结局、增量成本以及与再进行1次FIT或结肠镜检查相关的质量调整生命年(QALYG)。评估了筛查的最佳停止年龄,定义为增量成本效益比仍低于每QALYG 100,000美元支付意愿阈值的最高年龄。
用于验证模拟模型的2个PRECISE亚队列中的第一个包括25,974名成年人(15,060名女性[58.0%];54.7%年龄在76至80岁之间),在索引日期前10年结肠镜检查结果为阴性。第二个亚队列由118,269名成年人(67,058名女性[56.7%];90.5%年龄在76至80岁之间)组成,在索引日期前1年FIT结果为阴性。年龄较大、男性、合并症水平较高以及近期进行过CRC筛查与额外筛查的增量效益和成本效益降低相关。对于索引年龄前10年结肠镜检查结果为阴性且无合并症的76岁女性参考队列,再进行1次结肠镜检查每QALYG成本为38,226美元。对于具有其他等效特征的队列,对于索引年龄前10年结肠镜检查结果为阴性且无合并症的90岁女性,每QALYG相关成本增加到1,689,945美元;对于索引年龄前10年结肠镜检查结果为阴性且无合并症的76岁男性,每QALYG为51,604美元;对于索引年龄前10年结肠镜检查结果为阴性且有严重合并症的76岁女性,每QALYG为108,480美元,而对于索引年龄前30年结肠镜检查结果为阴性且无合并症的女性,每QALYG降至16,870美元。不同队列的最佳停止年龄对于结肠镜检查为小于76至86岁,对于FIT为小于76至88岁。
在这项经济评估中,年龄、性别、筛查史、合并症和未来筛查方式与CRC筛查的临床结局、成本效益和最佳停止年龄相关。这些结果可为指南制定和以患者为导向的知情决策提供参考。