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Lumbee Native American ancestry and the incidence of aggressive histologic subtypes of endometrial cancer

OBJECTIVE: The Lumbee Indian tribe is the largest Native American tribe in North Carolina, with about 55,000 enrolled members who mostly reside in southeastern counties. We evaluated whether Lumbee heritage is associated with high-risk histologic subtypes of endometrial cancer. METHODS: We retrospec...

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Autores principales: Zhang, Chelsea, Roque, Dario, Ehrisman, Jessie A., DiSanto, Nicola, Broadwater, Gloria, Doll, Kemi M., Gehrig, Paola A., Secord, Angeles Alvarez, Havrilesky, Laura J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563587/
https://www.ncbi.nlm.nih.gov/pubmed/26425722
http://dx.doi.org/10.1016/j.gore.2015.06.004
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author Zhang, Chelsea
Roque, Dario
Ehrisman, Jessie A.
DiSanto, Nicola
Broadwater, Gloria
Doll, Kemi M.
Gehrig, Paola A.
Secord, Angeles Alvarez
Havrilesky, Laura J.
author_facet Zhang, Chelsea
Roque, Dario
Ehrisman, Jessie A.
DiSanto, Nicola
Broadwater, Gloria
Doll, Kemi M.
Gehrig, Paola A.
Secord, Angeles Alvarez
Havrilesky, Laura J.
author_sort Zhang, Chelsea
collection PubMed
description OBJECTIVE: The Lumbee Indian tribe is the largest Native American tribe in North Carolina, with about 55,000 enrolled members who mostly reside in southeastern counties. We evaluated whether Lumbee heritage is associated with high-risk histologic subtypes of endometrial cancer. METHODS: We retrospectively analyzed the available records from IRB-approved endometrial cancer databases at two institutions of patients of Lumbee descent (year of diagnosis range 1980–2014). Each Lumbee case was matched by age, year of diagnosis, and BMI to two non-Lumbee controls. Chi-square test was used to compare categorical associations. Kaplan–Meier methods and log-rank test were used to display and compare disease-free survival (DFS) and overall survival (OS). Multivariate Cox proportional hazards regression was used to adjust for age and BMI while testing cohort as a predictor of DFS and OS. RESULTS: Among 108 subjects, 10/35 (29%) Lumbee and 19/72 (26%) non-Lumbee subjects had high-risk (serous/clear cell/carcinosarcoma) histologic types (p = 0.8). 12/35 (34%) Lumbee and 24/72 (33%) non-Lumbee subjects had grade 3 tumors (p = 0.9). 5/33 (15%) Lumbee and 13/72 (18%) non-Lumbee had advanced stage endometrial cancer at diagnosis (p = 0.7). Lumbee ancestry was not associated with worse survival outcomes. OS (p = 0.054) and DFS (p = 0.01) were both worse in Blacks compared to Lumbee and White subjects. CONCLUSION: In this retrospective cohort analysis, Lumbee Native American ancestry was not a significant independent predictor of rates of high-risk histological subtypes of endometrial cancer or poor survival outcomes.
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spelling pubmed-45635872015-09-30 Lumbee Native American ancestry and the incidence of aggressive histologic subtypes of endometrial cancer Zhang, Chelsea Roque, Dario Ehrisman, Jessie A. DiSanto, Nicola Broadwater, Gloria Doll, Kemi M. Gehrig, Paola A. Secord, Angeles Alvarez Havrilesky, Laura J. Gynecol Oncol Rep Case Series OBJECTIVE: The Lumbee Indian tribe is the largest Native American tribe in North Carolina, with about 55,000 enrolled members who mostly reside in southeastern counties. We evaluated whether Lumbee heritage is associated with high-risk histologic subtypes of endometrial cancer. METHODS: We retrospectively analyzed the available records from IRB-approved endometrial cancer databases at two institutions of patients of Lumbee descent (year of diagnosis range 1980–2014). Each Lumbee case was matched by age, year of diagnosis, and BMI to two non-Lumbee controls. Chi-square test was used to compare categorical associations. Kaplan–Meier methods and log-rank test were used to display and compare disease-free survival (DFS) and overall survival (OS). Multivariate Cox proportional hazards regression was used to adjust for age and BMI while testing cohort as a predictor of DFS and OS. RESULTS: Among 108 subjects, 10/35 (29%) Lumbee and 19/72 (26%) non-Lumbee subjects had high-risk (serous/clear cell/carcinosarcoma) histologic types (p = 0.8). 12/35 (34%) Lumbee and 24/72 (33%) non-Lumbee subjects had grade 3 tumors (p = 0.9). 5/33 (15%) Lumbee and 13/72 (18%) non-Lumbee had advanced stage endometrial cancer at diagnosis (p = 0.7). Lumbee ancestry was not associated with worse survival outcomes. OS (p = 0.054) and DFS (p = 0.01) were both worse in Blacks compared to Lumbee and White subjects. CONCLUSION: In this retrospective cohort analysis, Lumbee Native American ancestry was not a significant independent predictor of rates of high-risk histological subtypes of endometrial cancer or poor survival outcomes. Elsevier 2015-06-18 /pmc/articles/PMC4563587/ /pubmed/26425722 http://dx.doi.org/10.1016/j.gore.2015.06.004 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Series
Zhang, Chelsea
Roque, Dario
Ehrisman, Jessie A.
DiSanto, Nicola
Broadwater, Gloria
Doll, Kemi M.
Gehrig, Paola A.
Secord, Angeles Alvarez
Havrilesky, Laura J.
Lumbee Native American ancestry and the incidence of aggressive histologic subtypes of endometrial cancer
title Lumbee Native American ancestry and the incidence of aggressive histologic subtypes of endometrial cancer
title_full Lumbee Native American ancestry and the incidence of aggressive histologic subtypes of endometrial cancer
title_fullStr Lumbee Native American ancestry and the incidence of aggressive histologic subtypes of endometrial cancer
title_full_unstemmed Lumbee Native American ancestry and the incidence of aggressive histologic subtypes of endometrial cancer
title_short Lumbee Native American ancestry and the incidence of aggressive histologic subtypes of endometrial cancer
title_sort lumbee native american ancestry and the incidence of aggressive histologic subtypes of endometrial cancer
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563587/
https://www.ncbi.nlm.nih.gov/pubmed/26425722
http://dx.doi.org/10.1016/j.gore.2015.06.004
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