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Cancer screening and breast cancer family history in Spanish-speaking Hispanic/Latina women in California
BACKGROUND: Breast cancer is the most common cancer among women in the U.S. and the leading cause of cancer death among Hispanics/Latinas (H/L). H/L are less likely than Non-H/L White (NHW) women to be diagnosed in the early stages of this disease. Approximately 5-10% of breast cancer can be attribu...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643826/ https://www.ncbi.nlm.nih.gov/pubmed/36387260 http://dx.doi.org/10.3389/fonc.2022.940162 |
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author | Tamayo, Lizeth I. Perez, Fabian Perez, Angelica Hernandez, Miriam Martinez, Alejandra Huang, Xiaosong Zavala, Valentina A. Ziv, Elad Neuhausen, Susan L. Carvajal-Carmona, Luis G. Duron, Ysabel Fejerman, Laura |
author_facet | Tamayo, Lizeth I. Perez, Fabian Perez, Angelica Hernandez, Miriam Martinez, Alejandra Huang, Xiaosong Zavala, Valentina A. Ziv, Elad Neuhausen, Susan L. Carvajal-Carmona, Luis G. Duron, Ysabel Fejerman, Laura |
author_sort | Tamayo, Lizeth I. |
collection | PubMed |
description | BACKGROUND: Breast cancer is the most common cancer among women in the U.S. and the leading cause of cancer death among Hispanics/Latinas (H/L). H/L are less likely than Non-H/L White (NHW) women to be diagnosed in the early stages of this disease. Approximately 5-10% of breast cancer can be attributed to inherited genetic mutations in high penetrance genes such as BRCA1/2. Women with pathogenic variants in these genes have a 40-80% lifetime risk of breast cancer. Past studies have shown that genetic counseling can help women and their families make informed decisions about genetic testing and early cancer detection or risk-reduction strategies. However, H/L are 3.9-4.8 times less likely to undergo genetic testing than NHW women. We developed a program to outreach and educate the H/L community about hereditary breast cancer, targeting monolingual Spanish-speaking individuals in California. Through this program, we have assessed cancer screening behavior and identified women who might benefit from genetic counseling in a population that is usually excluded from cancer research and care. MATERIALS AND METHODS: The “Tu Historia Cuenta” program is a promotores-based virtual outreach and education program including the cities of San Francisco, Sacramento, and Los Angeles. Participants responded to three surveys: a demographic survey, a breast cancer family history survey, and a feedback survey. Survey responses were described for participants and compared by area where the program took place using chi-square, Fisher exact tests, and t tests. Multinomial logistic regression models were used for multivariate analyses. RESULTS AND CONCLUSION: We enrolled 1042 women, 892 completed the cancer family history survey and 62 (7%) provided responses compatible with referral to genetic counseling. We identified 272 women (42.8% ages 40 to 74 years) who were due for mammograms, 250 women (24.7% ages 25 to 65 years) due for Papanicolaou test, and 189 women (71.6% ages 50+) due for colorectal cancer screening. These results highlight the need of additional support for programs that spread awareness about cancer risk and facilitate access to resources, specifically within the H/L community. |
format | Online Article Text |
id | pubmed-9643826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96438262022-11-15 Cancer screening and breast cancer family history in Spanish-speaking Hispanic/Latina women in California Tamayo, Lizeth I. Perez, Fabian Perez, Angelica Hernandez, Miriam Martinez, Alejandra Huang, Xiaosong Zavala, Valentina A. Ziv, Elad Neuhausen, Susan L. Carvajal-Carmona, Luis G. Duron, Ysabel Fejerman, Laura Front Oncol Oncology BACKGROUND: Breast cancer is the most common cancer among women in the U.S. and the leading cause of cancer death among Hispanics/Latinas (H/L). H/L are less likely than Non-H/L White (NHW) women to be diagnosed in the early stages of this disease. Approximately 5-10% of breast cancer can be attributed to inherited genetic mutations in high penetrance genes such as BRCA1/2. Women with pathogenic variants in these genes have a 40-80% lifetime risk of breast cancer. Past studies have shown that genetic counseling can help women and their families make informed decisions about genetic testing and early cancer detection or risk-reduction strategies. However, H/L are 3.9-4.8 times less likely to undergo genetic testing than NHW women. We developed a program to outreach and educate the H/L community about hereditary breast cancer, targeting monolingual Spanish-speaking individuals in California. Through this program, we have assessed cancer screening behavior and identified women who might benefit from genetic counseling in a population that is usually excluded from cancer research and care. MATERIALS AND METHODS: The “Tu Historia Cuenta” program is a promotores-based virtual outreach and education program including the cities of San Francisco, Sacramento, and Los Angeles. Participants responded to three surveys: a demographic survey, a breast cancer family history survey, and a feedback survey. Survey responses were described for participants and compared by area where the program took place using chi-square, Fisher exact tests, and t tests. Multinomial logistic regression models were used for multivariate analyses. RESULTS AND CONCLUSION: We enrolled 1042 women, 892 completed the cancer family history survey and 62 (7%) provided responses compatible with referral to genetic counseling. We identified 272 women (42.8% ages 40 to 74 years) who were due for mammograms, 250 women (24.7% ages 25 to 65 years) due for Papanicolaou test, and 189 women (71.6% ages 50+) due for colorectal cancer screening. These results highlight the need of additional support for programs that spread awareness about cancer risk and facilitate access to resources, specifically within the H/L community. Frontiers Media S.A. 2022-10-26 /pmc/articles/PMC9643826/ /pubmed/36387260 http://dx.doi.org/10.3389/fonc.2022.940162 Text en Copyright © 2022 Tamayo, Perez, Perez, Hernandez, Martinez, Huang, Zavala, Ziv, Neuhausen, Carvajal-Carmona, Duron and Fejerman https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Tamayo, Lizeth I. Perez, Fabian Perez, Angelica Hernandez, Miriam Martinez, Alejandra Huang, Xiaosong Zavala, Valentina A. Ziv, Elad Neuhausen, Susan L. Carvajal-Carmona, Luis G. Duron, Ysabel Fejerman, Laura Cancer screening and breast cancer family history in Spanish-speaking Hispanic/Latina women in California |
title | Cancer screening and breast cancer family history in Spanish-speaking Hispanic/Latina women in California |
title_full | Cancer screening and breast cancer family history in Spanish-speaking Hispanic/Latina women in California |
title_fullStr | Cancer screening and breast cancer family history in Spanish-speaking Hispanic/Latina women in California |
title_full_unstemmed | Cancer screening and breast cancer family history in Spanish-speaking Hispanic/Latina women in California |
title_short | Cancer screening and breast cancer family history in Spanish-speaking Hispanic/Latina women in California |
title_sort | cancer screening and breast cancer family history in spanish-speaking hispanic/latina women in california |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643826/ https://www.ncbi.nlm.nih.gov/pubmed/36387260 http://dx.doi.org/10.3389/fonc.2022.940162 |
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