Impact of region of diagnosis, ethnicity, age, and gender on survival in acute myeloid leukemia (AML)
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Acharya, Utkarsh H.Halpern, Anna B.
Wu, Qian (Vicky)
Voutsinas, Jenna M.
Walter, Roland B.
Yun, Seongseok
Kanaan, Mohammed
Estey, Elihu H.
Affiliation
Univ Arizona, Canc Ctr, Div Hematol OncolIssue Date
2018
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TAYLOR & FRANCIS INCCitation
Utkarsh H. Acharya, Anna B. Halpern, Qian (Vicky) Wu, Jenna M. Voutsinas, Roland B. Walter, Seongseok Yun, Mohammed Kanaan & Elihu H. Estey (2018) Impact of region of diagnosis, ethnicity, age, and gender on survival in acute myeloid leukemia (AML), Journal of Drug Assessment, 7:1, 51-53, DOI: 10.1080/21556660.2018.1492925Journal
JOURNAL OF DRUG ASSESSMENTRights
© 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Aim: Acute myeloid leukemia (AML) is an aggressive hematopoietic clonal disorder characterized by the increased blasts and poor survival outcome, which is mainly driven by cytogenetic and molecular abnormalities. Here, we investigated the prognostic impact of other demographic parameters on the survival outcomes in AML patients. Method: We reviewed the Surveillance, Epidemiology, and End Result (SEER) database to collect demographic information, including age, diagnosis, gender, race, and geographic region in patients with non-acute promyelocytic leukemia AML, between 2004-2008. The primary end-point of our study was 3-year overall survival (OS), which was estimated by the Kaplan-Meier method and Cox regression model. Results: A total of 13,282 patients were included in our analyses. Increasing age (HR 1.2, p < .0001), male gender (HR 1.05, p = .01), and geographic region of Midwest (HR 1.07, p=.002) were associated with inferior 3-year OS in univariate analysis, and these parameters remained independent prognostic factors in multivariate analyses. Conclusions: AML is a heterogeneous myeloid neoplasm with patient outcomes largely dictated by the cytogenetics and somatic mutations. In our study, additional demographic factors, including advanced age, male gender, and geographic region of AML diagnosis were associated with OS outcome in non-APL AML patients.Note
Open access journalISSN
2155-6660PubMed ID
30034924Version
Final published versionAdditional Links
https://www.tandfonline.com/doi/full/10.1080/21556660.2018.1492925ae974a485f413a2113503eed53cd6c53
10.1080/21556660.2018.1492925
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