Evolving racial/ethnic disparities in AML survival in the novel therapy era

Abstract: Little is known about the impact of recent advances in acute myeloid leukemia (AML) treatment on racial/ethnic disparities in survival outcomes. We performed a retrospective cohort study of patients with newly diagnosed AML using data from a nationwide electronic health record–derived deid...

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Main Authors: Xin Wang, Phyllis A. Gimotty, Andrew H. Matthews, Ronac Mamtani, Selina M. Luger, Elizabeth O. Hexner, Daria V. Babushok, Shannon R. McCurdy, Noelle V. Frey, Ximena Jordan Bruno, Saar Gill, Mary Ellen Martin, Vikram R. Paralkar, Ivan Maillard, David L. Porter, Alison W. Loren, Alexander E. Perl, Keith W. Pratz, Kelly D. Getz, Catherine Lai
Format: Article
Language:English
Published: Elsevier 2025-02-01
Series:Blood Advances
Online Access:http://www.sciencedirect.com/science/article/pii/S2473952924006712
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author Xin Wang
Phyllis A. Gimotty
Andrew H. Matthews
Ronac Mamtani
Selina M. Luger
Elizabeth O. Hexner
Daria V. Babushok
Shannon R. McCurdy
Noelle V. Frey
Ximena Jordan Bruno
Saar Gill
Mary Ellen Martin
Vikram R. Paralkar
Ivan Maillard
David L. Porter
Alison W. Loren
Alexander E. Perl
Keith W. Pratz
Kelly D. Getz
Catherine Lai
author_facet Xin Wang
Phyllis A. Gimotty
Andrew H. Matthews
Ronac Mamtani
Selina M. Luger
Elizabeth O. Hexner
Daria V. Babushok
Shannon R. McCurdy
Noelle V. Frey
Ximena Jordan Bruno
Saar Gill
Mary Ellen Martin
Vikram R. Paralkar
Ivan Maillard
David L. Porter
Alison W. Loren
Alexander E. Perl
Keith W. Pratz
Kelly D. Getz
Catherine Lai
author_sort Xin Wang
collection DOAJ
description Abstract: Little is known about the impact of recent advances in acute myeloid leukemia (AML) treatment on racial/ethnic disparities in survival outcomes. We performed a retrospective cohort study of patients with newly diagnosed AML using data from a nationwide electronic health record–derived deidentified database. Patients were categorized based on their diagnosis date relative to venetoclax approval, as pre–novel therapy era (Pre era; 2014-2018; n = 2998) or post–novel therapy era (Post era; 2019-2022; n = 2098). Patients in the Post era were older and had more comorbidities than Pre era. Non-Hispanic Black (NHB) and Hispanic patients were younger and more likely to have lower socioeconomic status than non-Hispanic White (NHW) patients, with no differences in the distributions of key disease features. After accounting for age and comorbidity, overall survival (OS) was higher in patients in Post era than Pre era (adjusted hazard ratio [aHR], 0.90; 95% confidence interval [CI], 0.83-0.96). In Pre era, NHB had a 22% higher hazard of death than NHW (aHR, 1.22; 95% CI, 1.04-1.43), whereas worse OS was not observed for NHB in Post era (aHR, 0.86; 95% CI, 0.69-1.08; predicted 2-year survival, 45.3% vs 39.9%). Utilization of novel therapeutics in frontline therapy did not differ by race/ethnicity. Among patients receiving venetoclax-based induction, particularly those without TP53, RAS, or FLT3-ITD mutations, results suggested higher OS for NHB than NHW patients (aHR, 0.67; 95% CI, 0.45-1.01). Additional studies are needed to elucidate factors contributing to these observed survival differences and to inform strategies to optimize outcomes for all patients with AML.
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spelling doaj-art-033998285a0049908500e6c31b4f958c2025-01-31T05:12:10ZengElsevierBlood Advances2473-95292025-02-0193533544Evolving racial/ethnic disparities in AML survival in the novel therapy eraXin Wang0Phyllis A. Gimotty1Andrew H. Matthews2Ronac Mamtani3Selina M. Luger4Elizabeth O. Hexner5Daria V. Babushok6Shannon R. McCurdy7Noelle V. Frey8Ximena Jordan Bruno9Saar Gill10Mary Ellen Martin11Vikram R. Paralkar12Ivan Maillard13David L. Porter14Alison W. Loren15Alexander E. Perl16Keith W. Pratz17Kelly D. Getz18Catherine Lai19Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA; Leukemia Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY; Correspondence: Xin Wang, Leukemia Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, 530 E 74th St, New York, NY 10021;Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PADepartment of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; Division of Oncology, Children’s Hospital of Philadelphia, Philadelphia, PADivision of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PAAbstract: Little is known about the impact of recent advances in acute myeloid leukemia (AML) treatment on racial/ethnic disparities in survival outcomes. We performed a retrospective cohort study of patients with newly diagnosed AML using data from a nationwide electronic health record–derived deidentified database. Patients were categorized based on their diagnosis date relative to venetoclax approval, as pre–novel therapy era (Pre era; 2014-2018; n = 2998) or post–novel therapy era (Post era; 2019-2022; n = 2098). Patients in the Post era were older and had more comorbidities than Pre era. Non-Hispanic Black (NHB) and Hispanic patients were younger and more likely to have lower socioeconomic status than non-Hispanic White (NHW) patients, with no differences in the distributions of key disease features. After accounting for age and comorbidity, overall survival (OS) was higher in patients in Post era than Pre era (adjusted hazard ratio [aHR], 0.90; 95% confidence interval [CI], 0.83-0.96). In Pre era, NHB had a 22% higher hazard of death than NHW (aHR, 1.22; 95% CI, 1.04-1.43), whereas worse OS was not observed for NHB in Post era (aHR, 0.86; 95% CI, 0.69-1.08; predicted 2-year survival, 45.3% vs 39.9%). Utilization of novel therapeutics in frontline therapy did not differ by race/ethnicity. Among patients receiving venetoclax-based induction, particularly those without TP53, RAS, or FLT3-ITD mutations, results suggested higher OS for NHB than NHW patients (aHR, 0.67; 95% CI, 0.45-1.01). Additional studies are needed to elucidate factors contributing to these observed survival differences and to inform strategies to optimize outcomes for all patients with AML.http://www.sciencedirect.com/science/article/pii/S2473952924006712
spellingShingle Xin Wang
Phyllis A. Gimotty
Andrew H. Matthews
Ronac Mamtani
Selina M. Luger
Elizabeth O. Hexner
Daria V. Babushok
Shannon R. McCurdy
Noelle V. Frey
Ximena Jordan Bruno
Saar Gill
Mary Ellen Martin
Vikram R. Paralkar
Ivan Maillard
David L. Porter
Alison W. Loren
Alexander E. Perl
Keith W. Pratz
Kelly D. Getz
Catherine Lai
Evolving racial/ethnic disparities in AML survival in the novel therapy era
Blood Advances
title Evolving racial/ethnic disparities in AML survival in the novel therapy era
title_full Evolving racial/ethnic disparities in AML survival in the novel therapy era
title_fullStr Evolving racial/ethnic disparities in AML survival in the novel therapy era
title_full_unstemmed Evolving racial/ethnic disparities in AML survival in the novel therapy era
title_short Evolving racial/ethnic disparities in AML survival in the novel therapy era
title_sort evolving racial ethnic disparities in aml survival in the novel therapy era
url http://www.sciencedirect.com/science/article/pii/S2473952924006712
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