Validation of Microsimulation Models against Alternative Model Predictions and Long-Term Colorectal Cancer Incidence and Mortality Outcomes of Randomized Controlled Trials. (August 2020)
- Record Type:
- Journal Article
- Title:
- Validation of Microsimulation Models against Alternative Model Predictions and Long-Term Colorectal Cancer Incidence and Mortality Outcomes of Randomized Controlled Trials. (August 2020)
- Main Title:
- Validation of Microsimulation Models against Alternative Model Predictions and Long-Term Colorectal Cancer Incidence and Mortality Outcomes of Randomized Controlled Trials
- Authors:
- Lew, Jie-Bin
Greuter, Marjolein J. E.
Caruana, Michael
He, Emily
Worthington, Joachim
St John, D. James
Macrae, Finlay A.
Feletto, Eleonora
Coupé, Veerle M. H.
Canfell, Karen - Abstract:
- Background . This study aimed to assess the validity of 2 microsimulation models of colorectal cancer (CRC), Policy1-Bowel and ASCCA. Methods . The model-estimated CRC risk in population subgroups with different health statuses, "dwell time" (time from incident precancerous polyp to symptomatically detected CRC), and reduction in symptomatically detected CRC incidence after a one-time complete removal of polyps and/or undetected CRC were compared with published findings from 3 well-established models ( MISCAN, CRC-SPIN, and SimCRC ). Furthermore, 6 randomized controlled trials (RCTs) that provided screening using a guaiac fecal occult blood test (Funen trial, Burgundy trial, and Minnesota Colon Cancer Control Study [MCCCS]) or flexible sigmoidoscopy (NORCCAP, SCORE, and UKFSST) with long-term follow-up were simulated. Model-estimated long-term relative reductions of CRC incidence (RR inc ) and mortality (RR mort ) were compared with the RCTs' findings.Results . The Policy1-Bowel and ASCCA estimates showed more similarities to CRC-SPIN and SimCRC . For example, overall dwell times estimated by Policy1-Bowel (24.0 years) and ASCCA (25.3) were comparable to CRC-SPIN (25.8) and SimCRC (25.2) but higher than MISCAN (10.6). In addition, ∼86% of Policy1-Bowel 's and ∼74% of ASCCA 's estimated RR inc and RR mort were consistent with the RCTs' long-term follow-up findings. For example, at 17 to 18 years of follow-up, the MCCCS reported RR mort of 0.67 (95% confidence interval [CI],Background . This study aimed to assess the validity of 2 microsimulation models of colorectal cancer (CRC), Policy1-Bowel and ASCCA. Methods . The model-estimated CRC risk in population subgroups with different health statuses, "dwell time" (time from incident precancerous polyp to symptomatically detected CRC), and reduction in symptomatically detected CRC incidence after a one-time complete removal of polyps and/or undetected CRC were compared with published findings from 3 well-established models ( MISCAN, CRC-SPIN, and SimCRC ). Furthermore, 6 randomized controlled trials (RCTs) that provided screening using a guaiac fecal occult blood test (Funen trial, Burgundy trial, and Minnesota Colon Cancer Control Study [MCCCS]) or flexible sigmoidoscopy (NORCCAP, SCORE, and UKFSST) with long-term follow-up were simulated. Model-estimated long-term relative reductions of CRC incidence (RR inc ) and mortality (RR mort ) were compared with the RCTs' findings.Results . The Policy1-Bowel and ASCCA estimates showed more similarities to CRC-SPIN and SimCRC . For example, overall dwell times estimated by Policy1-Bowel (24.0 years) and ASCCA (25.3) were comparable to CRC-SPIN (25.8) and SimCRC (25.2) but higher than MISCAN (10.6). In addition, ∼86% of Policy1-Bowel 's and ∼74% of ASCCA 's estimated RR inc and RR mort were consistent with the RCTs' long-term follow-up findings. For example, at 17 to 18 years of follow-up, the MCCCS reported RR mort of 0.67 (95% confidence interval [CI], 0.51–0.83) and 0.79 (95% CI, 0.62–0.97) for the annual and biennial screening arm, respectively, and the UKFSST reported RR mort of 0.70 (95% CI, 0.62–0.79) for CRC at all sites and 0.54 (95% CI, 0.46–0.65) for distal CRC. The corresponding model estimates were 0.65, 0.74, 0.81, and 0.61, respectively, for Policy1-Bowel and 0.65, 0.70, 0.75, and 0.58, respectively, for ASCCA .Conclusion . Policy1-Bowel and ASCCA 's estimates are largely consistent with the data included for comparisons, which indicates good model validity. … (more)
- Is Part Of:
- Medical decision making. Volume 40:Number 6(2020)
- Journal:
- Medical decision making
- Issue:
- Volume 40:Number 6(2020)
- Issue Display:
- Volume 40, Issue 6 (2020)
- Year:
- 2020
- Volume:
- 40
- Issue:
- 6
- Issue Sort Value:
- 2020-0040-0006-0000
- Page Start:
- 815
- Page End:
- 829
- Publication Date:
- 2020-08
- Subjects:
- ASCCA -- colorectal cancer -- microsimulation -- Policy1-Bowel -- population modelling -- validation
Medical policy -- Periodicals
Clinical medicine -- Decision making -- Periodicals
Medicine -- Periodicals
Médecine clinique -- Prise de décision -- Périodiques
362.1 - Journal URLs:
- http://journals.sagepub.com/home/mdm ↗
http://www.ingenta.com/journals/browse/sage/j501 ↗
http://www.sagepublications.com/ ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=0272-989x;screen=info;ECOIP ↗ - DOI:
- 10.1177/0272989X20944869 ↗
- Languages:
- English
- ISSNs:
- 0272-989X
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- Legaldeposit
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