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Development and validation of a model to predict outcomes of colon cancer surveillance.
Rose, Johnie; Homa, Laura; Kong, Chung Yin; Cooper, Gregory S; Kattan, Michael W; Ermlich, Bridget O; Meyers, Jeffrey P; Primrose, John N; Pugh, Sian A; Shinkins, Bethany; Kim, Uriel; Meropol, Neal J.
Afiliação
  • Rose J; Case Western Reserve University School of Medicine, Cleveland, OH, USA. johnie.rose@case.edu.
  • Homa L; Case Comprehensive Cancer Center, Cleveland, OH, USA. johnie.rose@case.edu.
  • Kong CY; Case Western Reserve University School of Medicine, Cleveland, OH, USA.
  • Cooper GS; Massachusetts General Hospital Institute for Technology Assessment, Boston, MA, USA.
  • Kattan MW; Case Western Reserve University School of Medicine, Cleveland, OH, USA.
  • Ermlich BO; Case Comprehensive Cancer Center, Cleveland, OH, USA.
  • Meyers JP; University Hospitals Seidman Cancer Center, Cleveland, OH, USA.
  • Primrose JN; Case Comprehensive Cancer Center, Cleveland, OH, USA.
  • Pugh SA; Cleveland Clinic Foundation, Dept. of Quantitative Health Sciences, Cleveland, OH, USA.
  • Shinkins B; University Hospitals Cleveland Medical Center, Cleveland, OH, USA.
  • Kim U; Mayo Clinic Minnesota, Rochester, MN, USA.
  • Meropol NJ; University Surgery, Cancer Sciences, University of Southampton, Southampton, UK.
Cancer Causes Control ; 30(7): 767-778, 2019 Jul.
Article em En | MEDLINE | ID: mdl-31129907
ABSTRACT

PURPOSE:

Clinical trials suggest that intensive surveillance of colon cancer (CC) survivors to detect recurrence increases curative-intent treatment, although any survival benefit of surveillance as currently practiced appears modest. Realizing the potential of surveillance will require tools for identifying patients likely to benefit and for optimizing testing regimens. We describe and validate a model for predicting outcomes for any schedule of surveillance in CC survivors with specified age and cancer stage.

METHODS:

A Markov process parameterized based on individual-level clinical trial data generates natural history events for simulated patients. A utilization submodel simulates surveillance and diagnostic testing. We validate the model against outcomes from the follow-up after colorectal surgery (FACS) trial.

RESULTS:

Prevalidation sensitivity analysis showed no parameter influencing curative-intent treatment by > 5.0% or overall five-year survival (OS5) by > 1.5%. In validation, the proportion of recurring subjects predicted to receive curative-intent treatment fell within FACS 95% CI for carcinoembryonic antigen (CEA)-intensive, computed tomography (CT)-intensive, and combined CEA+CT regimens, but not for a minimum surveillance regimen, where the model overestimated recurrence and curative treatment. The observed OS5 fell within 95% prediction intervals for all regimens.

CONCLUSION:

The model performed well in predicting curative surgery for three of four FACS arms. It performed well in predicting OS5 for all arms.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / Modelos Teóricos / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Aged / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / Modelos Teóricos / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Aged / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article