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Evolving racial/ethnic disparities in AML survival in the novel therapy era.
Wang, Xin; Gimotty, Phyllis A; Matthews, Andrew H; Mamtani, Ronac; Luger, Selina M; Hexner, Elizabeth O; Babushok, Daria V; McCurdy, Shannon R; Frey, Noelle V; Bruno, Ximena Jordan; Gill, Saar; Martin, Mary Ellen; Paralkar, Vikram R; Maillard, Ivan; Porter, David L; Loren, Alison W; Perl, Alexander E; Pratz, Keith W; Getz, Kelly D; Lai, Catherine.
Afiliação
  • Wang X; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Gimotty PA; Leukemia Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Matthews AH; Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Mamtani R; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Luger SM; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Hexner EO; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Babushok DV; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • McCurdy SR; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Frey NV; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Bruno XJ; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Gill S; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Martin ME; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Paralkar VR; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Maillard I; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Porter DL; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Loren AW; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Perl AE; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Pratz KW; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Getz KD; Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Lai C; Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Blood Adv ; 9(3): 533-544, 2025 Feb 11.
Article em En | MEDLINE | ID: mdl-39888631
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Tipos_de_cancer / Outros_tipos Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Disparidades em Assistência à Saúde Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood adv Ano de publicação: 2025 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Tipos_de_cancer / Outros_tipos Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Disparidades em Assistência à Saúde Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood adv Ano de publicação: 2025 Tipo de documento: Article