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Development and validation of a model to predict outcomes of colon cancer surveillance

Development and validation of a model to predict outcomes of colon cancer surveillance
Development and validation of a model to predict outcomes of colon cancer surveillance
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.
0957-5243
767–778
Rose, Johnie
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Homa, Laura
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Kong, Chung Yin
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Cooper, Gregory
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Kattan, Michael
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Ermlich, Bridget
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Meyers, Jeffrey
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Primrose, John
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Pugh, Sian
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Shinkins, Bethany
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Kim, Uriel
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Meropol, Neal
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Rose, Johnie
c10a33ef-756b-4aa4-9733-6d1f869ec045
Homa, Laura
4dbf11a2-69a1-425a-953a-4865ec3fab1a
Kong, Chung Yin
b88bd4f2-0822-49d8-a671-23e3abd9bb5b
Cooper, Gregory
478ece57-6517-499d-8cc9-2a10131b9a4b
Kattan, Michael
bd437fa0-7f90-458d-a99d-60dcee1d689c
Ermlich, Bridget
595fc85c-74f9-4ba6-911c-b4ed162250bd
Meyers, Jeffrey
d77b8c02-58c5-405b-81da-b10668b3cf28
Primrose, John
d85f3b28-24c6-475f-955b-ec457a3f9185
Pugh, Sian
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Shinkins, Bethany
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Kim, Uriel
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Meropol, Neal
b51e003e-a041-428d-ae6b-8fadf2226871

Rose, Johnie, Homa, Laura, Kong, Chung Yin, Cooper, Gregory, Kattan, Michael, Ermlich, Bridget, Meyers, Jeffrey, Primrose, John, Pugh, Sian, Shinkins, Bethany, Kim, Uriel and Meropol, Neal (2019) Development and validation of a model to predict outcomes of colon cancer surveillance. Cancer Causes & Control, 30 (7), 767–778. (doi:10.1007/s10552-019-01187-x).

Record type: Article

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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Manuscript CRCSuRE Validation FACS CCC 1-24-19 - Accepted Manuscript
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Accepted/In Press date: 16 May 2019
e-pub ahead of print date: 25 May 2019
Published date: July 2019

Identifiers

Local EPrints ID: 431144
URI: http://eprints.soton.ac.uk/id/eprint/431144
ISSN: 0957-5243
PURE UUID: a7d805cf-a1ea-4ccf-b14a-da8b6f6ab317
ORCID for John Primrose: ORCID iD orcid.org/0000-0002-2069-7605

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Date deposited: 24 May 2019 16:30
Last modified: 16 Mar 2024 07:52

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Contributors

Author: Johnie Rose
Author: Laura Homa
Author: Chung Yin Kong
Author: Gregory Cooper
Author: Michael Kattan
Author: Bridget Ermlich
Author: Jeffrey Meyers
Author: John Primrose ORCID iD
Author: Sian Pugh
Author: Bethany Shinkins
Author: Uriel Kim
Author: Neal Meropol

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