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Synergistic markers based on inter-covariate association estimate treatment option with lower propensity to covariates

BACKGROUND: Propensity constitutes a common problem in identifying clinical outcome prediction model whose covariates include the treatment option, which is assumed to be randomly assigned but indeed dependent of other covariates in the training data. The genuine effect of treatment option cannot be...

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Autores principales: Chan, Lawrence Wing Chi, Sihoe, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477640/
https://www.ncbi.nlm.nih.gov/pubmed/37675295
http://dx.doi.org/10.21037/atm-22-5006
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author Chan, Lawrence Wing Chi
Sihoe, Alan
author_facet Chan, Lawrence Wing Chi
Sihoe, Alan
author_sort Chan, Lawrence Wing Chi
collection PubMed
description BACKGROUND: Propensity constitutes a common problem in identifying clinical outcome prediction model whose covariates include the treatment option, which is assumed to be randomly assigned but indeed dependent of other covariates in the training data. The genuine effect of treatment option cannot be elucidated under the influence of propensity. Existing approaches, such as matched-pairs study design, still cannot solve the problem for imbalanced or small datasets. METHODS: This work proposed an anti-propensity estimate of treatment option, which is generated by support vector classifier based on two synergistic markers that represent the lower and upper limits of inter-covariate association level. The algorithm for generating the synergistic markers was illustrated and the performance was evaluated on a public dataset of gene expression levels, which were obtained from surgically excised tumor samples in non-small cell lung cancer (NSCLC) patients where treatment option, i.e., adjuvant therapy or not, was known. RESULTS: Six covariates represented by the expression levels of ZNF217, ERCC3, PMS1, PIK3CB, BARD1, and MAPK1, were selected to generate two synergistic markers and classifier for estimating the adjuvant therapy option with substantially attenuated propensity. The estimation accuracy attained an area under the receiver-operating characteristics curve, 0.78, in the test set. CONCLUSIONS: The proposed synergistic markers demonstrated a parsimonious and anti-propensity estimation of treatment option, which is ready for the further evaluation and application in the clinical outcome prediction model.
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spelling pubmed-104776402023-09-06 Synergistic markers based on inter-covariate association estimate treatment option with lower propensity to covariates Chan, Lawrence Wing Chi Sihoe, Alan Ann Transl Med Original Article BACKGROUND: Propensity constitutes a common problem in identifying clinical outcome prediction model whose covariates include the treatment option, which is assumed to be randomly assigned but indeed dependent of other covariates in the training data. The genuine effect of treatment option cannot be elucidated under the influence of propensity. Existing approaches, such as matched-pairs study design, still cannot solve the problem for imbalanced or small datasets. METHODS: This work proposed an anti-propensity estimate of treatment option, which is generated by support vector classifier based on two synergistic markers that represent the lower and upper limits of inter-covariate association level. The algorithm for generating the synergistic markers was illustrated and the performance was evaluated on a public dataset of gene expression levels, which were obtained from surgically excised tumor samples in non-small cell lung cancer (NSCLC) patients where treatment option, i.e., adjuvant therapy or not, was known. RESULTS: Six covariates represented by the expression levels of ZNF217, ERCC3, PMS1, PIK3CB, BARD1, and MAPK1, were selected to generate two synergistic markers and classifier for estimating the adjuvant therapy option with substantially attenuated propensity. The estimation accuracy attained an area under the receiver-operating characteristics curve, 0.78, in the test set. CONCLUSIONS: The proposed synergistic markers demonstrated a parsimonious and anti-propensity estimation of treatment option, which is ready for the further evaluation and application in the clinical outcome prediction model. AME Publishing Company 2023-04-12 2023-08-30 /pmc/articles/PMC10477640/ /pubmed/37675295 http://dx.doi.org/10.21037/atm-22-5006 Text en 2023 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Chan, Lawrence Wing Chi
Sihoe, Alan
Synergistic markers based on inter-covariate association estimate treatment option with lower propensity to covariates
title Synergistic markers based on inter-covariate association estimate treatment option with lower propensity to covariates
title_full Synergistic markers based on inter-covariate association estimate treatment option with lower propensity to covariates
title_fullStr Synergistic markers based on inter-covariate association estimate treatment option with lower propensity to covariates
title_full_unstemmed Synergistic markers based on inter-covariate association estimate treatment option with lower propensity to covariates
title_short Synergistic markers based on inter-covariate association estimate treatment option with lower propensity to covariates
title_sort synergistic markers based on inter-covariate association estimate treatment option with lower propensity to covariates
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477640/
https://www.ncbi.nlm.nih.gov/pubmed/37675295
http://dx.doi.org/10.21037/atm-22-5006
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