TY - JOUR
T1 - Comparison of performance between a short categorized lifestyle exposure-based colon cancer risk prediction tool and a model using continuous measures
AU - Liu, Ying
AU - Colditz, Graham A.
AU - Rosner, Bernard A.
AU - Dart, Hank
AU - Wei, Esther
AU - Waters, Erika A.
N1 - Funding Information:
We would like to thank the participants and staff of the Nurses' Health Study and the Health Professional Follow-up Study, the Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School for their valuable contributions. We also thank the following state cancer registries for their help: AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KY, LA, ME, MD, MA, MI, NE, NH, NJ, NY, NC, ND, OH, OK, OR, PA, RI, SC, TN, TX, VA, WA, WY. The authors assume full responsibility for analyses and interpretation of these data. This study was supported by a research grant from the NIH (R01CA190391). Y. Liu, G. Colditz, and E. Waters were supported by the NCI (R01CA190391 and P30 CA091842) and the Foundation for Barnes Jewish Hospital (St. Louis, MO). The Nurses' Health Study (UM1CA186107; P01CA87969) and the Health Professional Follow-Up Study (UM1CA167552) were supported by the NIH.
Publisher Copyright:
© 2018 American Association for Cancer Research.
PY - 2018/12
Y1 - 2018/12
N2 - Risk prediction models that estimate an individual's risk of developing colon cancer could be used for a variety of clinical and public health interventions, including offering high-risk individuals enhanced screening or lifestyle interventions. However, if risk prediction models are to be translated into actual clinical and public health practice, they must not only be valid and reliable, but also be easy to use. One way of accomplishing this might be to simplify the information that users of risk prediction tools have to enter, but it is critical to ensure no resulting detrimental effects on model performance. We compared the performance of a simplified, largely categorized exposure-based colon cancer risk model against a more complex, largely continuous exposure-based risk model using two prospective cohorts. Using data from the Nurses' Health Study and the Health Professionals Follow-up Study we included 816 incident colon cancer cases in women and 412 in men. The discrimination of models was not significantly different comparing a categorized risk prediction model with a continuous prediction model in women (c-statistic 0.600 vs. 0.609, Pdiff ¼ 0.07) and men (c-statistic 0.622 vs. 0.618, Pdiff ¼ 0.60). Both models had good calibration in men [observed case count/ expected case count (O/E) ¼ 1.05, P > 0.05] but not in women (O/E ¼ 1.19, P < 0.01). Risk reclassification was slightly improved using categorized predictors in men [net reclassification index (NRI) ¼ 0.041] and slightly worsened in women (NRI ¼ 0.065). Categorical assessment of predictor variables may facilitate use of risk assessment tools in the general population without significant loss of performance. Cancer Prev Res; 11(12); 841-8. 2018 AACR.
AB - Risk prediction models that estimate an individual's risk of developing colon cancer could be used for a variety of clinical and public health interventions, including offering high-risk individuals enhanced screening or lifestyle interventions. However, if risk prediction models are to be translated into actual clinical and public health practice, they must not only be valid and reliable, but also be easy to use. One way of accomplishing this might be to simplify the information that users of risk prediction tools have to enter, but it is critical to ensure no resulting detrimental effects on model performance. We compared the performance of a simplified, largely categorized exposure-based colon cancer risk model against a more complex, largely continuous exposure-based risk model using two prospective cohorts. Using data from the Nurses' Health Study and the Health Professionals Follow-up Study we included 816 incident colon cancer cases in women and 412 in men. The discrimination of models was not significantly different comparing a categorized risk prediction model with a continuous prediction model in women (c-statistic 0.600 vs. 0.609, Pdiff ¼ 0.07) and men (c-statistic 0.622 vs. 0.618, Pdiff ¼ 0.60). Both models had good calibration in men [observed case count/ expected case count (O/E) ¼ 1.05, P > 0.05] but not in women (O/E ¼ 1.19, P < 0.01). Risk reclassification was slightly improved using categorized predictors in men [net reclassification index (NRI) ¼ 0.041] and slightly worsened in women (NRI ¼ 0.065). Categorical assessment of predictor variables may facilitate use of risk assessment tools in the general population without significant loss of performance. Cancer Prev Res; 11(12); 841-8. 2018 AACR.
UR - http://www.scopus.com/inward/record.url?scp=85058323760&partnerID=8YFLogxK
U2 - 10.1158/1940-6207.CAPR-18-0196
DO - 10.1158/1940-6207.CAPR-18-0196
M3 - Article
C2 - 30446519
AN - SCOPUS:85058323760
SN - 1940-6207
VL - 11
SP - 841
EP - 848
JO - Cancer Prevention Research
JF - Cancer Prevention Research
IS - 12
ER -