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. 2024 Dec 30;24(1):1596.
doi: 10.1186/s12885-024-13319-x.

Age, frequency, and strategy optimization for organized colorectal cancer screening: a decision analysis conducted in China for the years 2023-2038

Affiliations

Age, frequency, and strategy optimization for organized colorectal cancer screening: a decision analysis conducted in China for the years 2023-2038

Zixing Wang et al. BMC Cancer. .

Abstract

Background: The colorectal cancer mortality rate in China has exceeded that in many developing countries and is expected to further increase owing to multiple factors, including the aging population. However, the optimal policy for colorectal cancer screening is unknown.

Methods: We synthesized the most up-to-date data using a 12-state Markov model populated with a cohort of Chinese men and women born during 1949-1988, and evaluated 16 conventional and 40 risk-tailored schemes for colorectal cancer screening, considering possible combinations of age (starting at 40 + years and ending at 75 years), frequency, and strategy (standard colonoscopy, fecal immunochemical testing with colonoscopy if positive, or risk-tailored). We projected the incidence and mortality of CRC, cost, and quality-adjusted life years for 2023-2038; and performed incremental cost-effectiveness, probability acceptability, and sensitivity analyses to identify the optimal scheme and the factors affecting this choice.

Results: By 2038, all standard colonoscopy, colonoscopy following fecal immunochemical testing, and risk-tailored schemes were effective in reshaping China's colorectal cancer trajectory, with relative reductions in colorectal cancer incidence and mortality rates of up to 34% and 33.7%, respectively, versus no screening. Two standard colonoscopy, one colonoscopy following fecal immunochemical testing, and four risk-tailored schemes were efficient using a starting age of 40 years. Among these options, a risk-tailored scheme (standard colonoscopy every 5 years for high-risk and annual fecal immunochemical testing screening for moderate-to-low-risk) had a high probability (31.1%) of being optimal (with ≥ 40% uptake for a high-risk population, in particular), given China's present per capita gross domestic product, and would yield the highest gain in quality-adjusted life years in 17 of 31 provinces.

Conclusions: Our findings suggest the commencement of colorectal cancer screening at 40 years of age in China, and that risk-tailored and some conventional schemes would be effective and cost-efficient. These findings should be valuable for policy-making regarding cancer control and resource allocation.

Keywords: Cancer screening; Colorectal cancer; Cost effectiveness; Decision analysis; Early onset.

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Conflict of interest statement

Declarations. Ethics approval and consent to participate: Not applicable. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
The Markov state transition decision model used. The green lines indicate that resected pre-cancerous lesions can either regress to a “no adenoma” status or progress to colorectal cancer (CRC). For resected stage II and stage III CRC, the lesions are considered to regress to stage I
Fig. 2
Fig. 2
Projected cumulative incidences of CRC and CRC-related mortality. C5_X and C10_X denote colonoscopy screening every 5 and 10 years from X years of age, respectively. F1_Y and F2_Y denote annual and biennial fecal immunochemical testing from Y years of age, respectively. Similar notations apply for risk-tailored schemes, where C denotes colonoscopy for the high-risk population and F denotes fecal immunochemical testing for the low-risk population
Fig. 3
Fig. 3
Cost-effectiveness plane. C5_X and C10_X denote colonoscopy screening every 5 and 10 years from X years of age, respectively. F1_Y and F2_Y denote annual and biennial fecal immunochemical testing from Y years of age, respectively. Similar notations apply for risk-tailored schemes, where C denotes colonoscopy for the high-risk population and F denotes fecal immunochemical testing for the low-risk population
Fig. 4
Fig. 4
Optimal schemes according to colonoscopy participation rate. C5_X and C10_X denote colonoscopy screening every 5 and 10 years from X years of age, respectively. F1_Y and F2_Y denote annual and biennial fecal immunochemical testing from Y years of age, respectively. Similar notations apply for risk-tailored schemes, where C denotes colonoscopy for the high-risk population and F denotes fecal immunochemical testing for the low-risk population

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