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Gender and ethnic differences in chronic myelogenous leukemia prognosis and treatment response: a single-institution retrospective study
BACKGROUND: In the last decade the importance of ethnicity, socio-economic and gender differences in relation to disease incidence, diagnosis, and prognosis has been realized. Differences in these areas have become a major health policy focus in the United States. Our study was undertaken to examine...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2727534/ https://www.ncbi.nlm.nih.gov/pubmed/19630970 http://dx.doi.org/10.1186/1756-8722-2-30 |
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author | Lee, Justin P Birnstein, Elliott Masiello, David Yang, Dongyun Yang, Allen S |
author_facet | Lee, Justin P Birnstein, Elliott Masiello, David Yang, Dongyun Yang, Allen S |
author_sort | Lee, Justin P |
collection | PubMed |
description | BACKGROUND: In the last decade the importance of ethnicity, socio-economic and gender differences in relation to disease incidence, diagnosis, and prognosis has been realized. Differences in these areas have become a major health policy focus in the United States. Our study was undertaken to examine the demographic and clinical features of chronic myelogenous leukemia (CML) patients presenting initially at the LAC+USC Medical Center, which serves an ethnically diverse population. RESULTS: Patients were evenly split by gender, overwhelmingly Hispanic (60.9%), and quite young (median age 39, range 17–65) compared with previously reported CML patient populations. Previous CML studies identified significant anemia (Hgb <12 g/dl), significant thrombocytosis (platelets >450 × 10(9)/l), and significant leukocytosis (WBC >50 × 10(9)/l) as significant adverse pretreatment prognostic factors. Using these indicators, in addition to the validated Hasford and Sokal scores, patients were stratified and analyzed via gender and ethnicity. A significantly greater proportion of women presented with significant anemia (p = 0.019, Fisher's exact test) and significant thrombocytosis (p = 0.041, Fisher's exact test) compared to men, although no differences were found in risk stratification or treatment response. MCV values for women were significantly (p = 0.02, 2-sample t-test) lower than those for men, suggesting iron deficiency anemia. Focusing on ethnicity, Hispanics as a whole had significantly lower Hasford risk stratification (p = 0.046, Fisher's exact test), and significantly greater likelihood (p = 0.016, Fisher's exact test) of achieving 3-month complete haematological remission (CHR) compared with non-Hispanics at LAC+USC Medical Center, though differences in treatment outcome were no longer significant with analysis limited to patients treated with first-line imatinib. CONCLUSION: Female CML patients at LAC+USC Medical Center present with more significant adverse pre-treatment prognostic factors compared to men, but achieve comparable outcomes. Hispanic patients present with lower risk profile CML and achieve better treatment responses compared to non-Hispanic patients as a whole; these ethnic differences are no longer significant when statistical analysis is limited to patients given imatinib as first-line therapy. Our patients achieve response rates inferior to those of large-scale national studies. This constellation of findings has not been reported in previous studies, and is likely reflective of a unique patient population. |
format | Text |
id | pubmed-2727534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27275342009-08-15 Gender and ethnic differences in chronic myelogenous leukemia prognosis and treatment response: a single-institution retrospective study Lee, Justin P Birnstein, Elliott Masiello, David Yang, Dongyun Yang, Allen S J Hematol Oncol Research BACKGROUND: In the last decade the importance of ethnicity, socio-economic and gender differences in relation to disease incidence, diagnosis, and prognosis has been realized. Differences in these areas have become a major health policy focus in the United States. Our study was undertaken to examine the demographic and clinical features of chronic myelogenous leukemia (CML) patients presenting initially at the LAC+USC Medical Center, which serves an ethnically diverse population. RESULTS: Patients were evenly split by gender, overwhelmingly Hispanic (60.9%), and quite young (median age 39, range 17–65) compared with previously reported CML patient populations. Previous CML studies identified significant anemia (Hgb <12 g/dl), significant thrombocytosis (platelets >450 × 10(9)/l), and significant leukocytosis (WBC >50 × 10(9)/l) as significant adverse pretreatment prognostic factors. Using these indicators, in addition to the validated Hasford and Sokal scores, patients were stratified and analyzed via gender and ethnicity. A significantly greater proportion of women presented with significant anemia (p = 0.019, Fisher's exact test) and significant thrombocytosis (p = 0.041, Fisher's exact test) compared to men, although no differences were found in risk stratification or treatment response. MCV values for women were significantly (p = 0.02, 2-sample t-test) lower than those for men, suggesting iron deficiency anemia. Focusing on ethnicity, Hispanics as a whole had significantly lower Hasford risk stratification (p = 0.046, Fisher's exact test), and significantly greater likelihood (p = 0.016, Fisher's exact test) of achieving 3-month complete haematological remission (CHR) compared with non-Hispanics at LAC+USC Medical Center, though differences in treatment outcome were no longer significant with analysis limited to patients treated with first-line imatinib. CONCLUSION: Female CML patients at LAC+USC Medical Center present with more significant adverse pre-treatment prognostic factors compared to men, but achieve comparable outcomes. Hispanic patients present with lower risk profile CML and achieve better treatment responses compared to non-Hispanic patients as a whole; these ethnic differences are no longer significant when statistical analysis is limited to patients given imatinib as first-line therapy. Our patients achieve response rates inferior to those of large-scale national studies. This constellation of findings has not been reported in previous studies, and is likely reflective of a unique patient population. BioMed Central 2009-07-24 /pmc/articles/PMC2727534/ /pubmed/19630970 http://dx.doi.org/10.1186/1756-8722-2-30 Text en Copyright © 2009 Lee et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Lee, Justin P Birnstein, Elliott Masiello, David Yang, Dongyun Yang, Allen S Gender and ethnic differences in chronic myelogenous leukemia prognosis and treatment response: a single-institution retrospective study |
title | Gender and ethnic differences in chronic myelogenous leukemia prognosis and treatment response: a single-institution retrospective study |
title_full | Gender and ethnic differences in chronic myelogenous leukemia prognosis and treatment response: a single-institution retrospective study |
title_fullStr | Gender and ethnic differences in chronic myelogenous leukemia prognosis and treatment response: a single-institution retrospective study |
title_full_unstemmed | Gender and ethnic differences in chronic myelogenous leukemia prognosis and treatment response: a single-institution retrospective study |
title_short | Gender and ethnic differences in chronic myelogenous leukemia prognosis and treatment response: a single-institution retrospective study |
title_sort | gender and ethnic differences in chronic myelogenous leukemia prognosis and treatment response: a single-institution retrospective study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2727534/ https://www.ncbi.nlm.nih.gov/pubmed/19630970 http://dx.doi.org/10.1186/1756-8722-2-30 |
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