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Lowering the colorectal cancer screening age improves predicted outcomes in a microsimulation model
Deborah A Fisher1, Leila Saoud2, Lila J Finney Rutten3
1Department of Medicine, Division of Gastroenterology, Duke University, Durham, NC, USA.
Current Medical Research and Opinion
|March 26, 2021
Summary
Lowering colorectal cancer screening age to 45 improves outcomes. Triennial multi-target stool DNA (mt-sDNA) screening offers greater benefits than annual fecal immunochemical test (FIT) when using real-world adherence rates.
Area of Science:
- Oncology
- Preventive Medicine
- Health Services Research
Background:
- Colorectal cancer (CRC) incidence is rising in younger populations.
- Current guidelines recommend CRC screening initiation at age 50 for average-risk individuals.
- There is a growing trend to lower the recommended screening age to 45.
Purpose of the Study:
- To model the impact of lowering CRC screening initiation age from 50 to 45 years.
- To compare triennial multi-target stool DNA (mt-sDNA) and annual fecal immunochemical test (FIT) screening strategies.
- To incorporate theoretical and reported adherence rates into the screening models.
Main Methods:
- Simulated screening strategies for individuals aged 40 without CRC.
- Modeled screening from ages 50-75 versus 45-75.
- Calculated CRC incidence, mortality, and life-years gained (LYG) using perfect (100%) and reported adherence rates (71% mt-sDNA; 43% FIT).
Main Results:
- Lowering screening initiation to age 45 increased predicted life-years gained (LYG) by 22.2-24.4 per 1000 individuals.
- Initiation at age 45 reduced CRC cases and deaths compared to age 50, particularly with reported adherence.
- With reported adherence, mt-sDNA averted more CRC cases (8.6) and deaths (3.3) per 1000 individuals than FIT.
Conclusions:
- Lowering CRC screening initiation age to 45 improves estimated screening outcomes.
- Triennial mt-sDNA screening demonstrates greater benefits than annual FIT screening when reported adherence rates are considered.
- These findings support the potential benefits of earlier CRC screening and highlight differences in screening test effectiveness based on adherence.

