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Assessment of common risk factors and validation of the Gail model for breast cancer: A hospital-based study from Western India

OBJECTIVE: Modified Gail Model is a noninvasive, easy to implement risk estimation tool for absolute breast cancer risk. It was developed with data collected from non African American females and further modified for African-American, the Hispanic, and Native American populations. The use of this mo...

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Autores principales: Kumar, Naveen, Singh, Vinit, Mehta, Garima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7605293/
https://www.ncbi.nlm.nih.gov/pubmed/33163382
http://dx.doi.org/10.4103/tcmj.tcmj_171_19
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author Kumar, Naveen
Singh, Vinit
Mehta, Garima
author_facet Kumar, Naveen
Singh, Vinit
Mehta, Garima
author_sort Kumar, Naveen
collection PubMed
description OBJECTIVE: Modified Gail Model is a noninvasive, easy to implement risk estimation tool for absolute breast cancer risk. It was developed with data collected from non African American females and further modified for African-American, the Hispanic, and Native American populations. The use of this model for population outside the US and European country is not yet validated. We evaluated the prevalent risk factors and the effectiveness of the Gail model for risk assessment in our local Indian population. MATERIALS AND METHODS: A retrospective analysis of a prospectively maintained database was conducted on patients treated between 2008 and 2013. Six hundred and fifty patients were included in each group. Six questions were taken as per the breast cancer risk assessment tool calculator. A value of over 1.67% was taken as a high risk for breast cancer development. RESULTS: The mean age of the participant was 50 ± 21.3 years in cases and 41 ± 16.4 years in controls. Age and age at first childbirth >30 years were found to be significant and associated with increased risk of breast carcinoma, but the age at menarche, family history, previous breast biopsy, and atypical hyperplasia was no significant. The Gail model was assessed, and sensitivity was 10.30% and 96.30% specificity for our population. Positive and negative predictive values were 73.62% and 51.77%. CONCLUSION: Our study concluded that the Gail model is not an appropriate risk assessment tool for the population in its present form. For the future application of this model, we need to perform a bigger study with a higher sample size representing a maximum number of local variabilities in the Indian population.
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spelling pubmed-76052932020-11-05 Assessment of common risk factors and validation of the Gail model for breast cancer: A hospital-based study from Western India Kumar, Naveen Singh, Vinit Mehta, Garima Tzu Chi Med J Original Article OBJECTIVE: Modified Gail Model is a noninvasive, easy to implement risk estimation tool for absolute breast cancer risk. It was developed with data collected from non African American females and further modified for African-American, the Hispanic, and Native American populations. The use of this model for population outside the US and European country is not yet validated. We evaluated the prevalent risk factors and the effectiveness of the Gail model for risk assessment in our local Indian population. MATERIALS AND METHODS: A retrospective analysis of a prospectively maintained database was conducted on patients treated between 2008 and 2013. Six hundred and fifty patients were included in each group. Six questions were taken as per the breast cancer risk assessment tool calculator. A value of over 1.67% was taken as a high risk for breast cancer development. RESULTS: The mean age of the participant was 50 ± 21.3 years in cases and 41 ± 16.4 years in controls. Age and age at first childbirth >30 years were found to be significant and associated with increased risk of breast carcinoma, but the age at menarche, family history, previous breast biopsy, and atypical hyperplasia was no significant. The Gail model was assessed, and sensitivity was 10.30% and 96.30% specificity for our population. Positive and negative predictive values were 73.62% and 51.77%. CONCLUSION: Our study concluded that the Gail model is not an appropriate risk assessment tool for the population in its present form. For the future application of this model, we need to perform a bigger study with a higher sample size representing a maximum number of local variabilities in the Indian population. Wolters Kluwer - Medknow 2020-04-10 /pmc/articles/PMC7605293/ /pubmed/33163382 http://dx.doi.org/10.4103/tcmj.tcmj_171_19 Text en Copyright: © 2020 Tzu Chi Medical Journal http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Kumar, Naveen
Singh, Vinit
Mehta, Garima
Assessment of common risk factors and validation of the Gail model for breast cancer: A hospital-based study from Western India
title Assessment of common risk factors and validation of the Gail model for breast cancer: A hospital-based study from Western India
title_full Assessment of common risk factors and validation of the Gail model for breast cancer: A hospital-based study from Western India
title_fullStr Assessment of common risk factors and validation of the Gail model for breast cancer: A hospital-based study from Western India
title_full_unstemmed Assessment of common risk factors and validation of the Gail model for breast cancer: A hospital-based study from Western India
title_short Assessment of common risk factors and validation of the Gail model for breast cancer: A hospital-based study from Western India
title_sort assessment of common risk factors and validation of the gail model for breast cancer: a hospital-based study from western india
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7605293/
https://www.ncbi.nlm.nih.gov/pubmed/33163382
http://dx.doi.org/10.4103/tcmj.tcmj_171_19
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