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Disparities in receiving disease-directed therapy, allogeneic stem cell transplantation in non-Hispanic Black patients with TP53-mutated acute myeloid leukemia.
Badar, Talha; Litzow, Mark R; Shallis, Rory M; Patel, Anand; Saliba, Antoine N; Burkart, Madelyn; Bewersdorf, Jan P; Stahl, Maximilian; De Camargo Correia, Guilherme Sacchi; Guru Murthy, Guru Subramanian; Abaza, Yasmin; Duvall, Adam; Bradshaw, Danielle; Kota, Vamsi; Dinner, Shira; Goldberg, Aaron D; Palmisiano, Neil; Al Kali, Aref; Atallah, Ehab.
Afiliación
  • Badar T; Division of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, Florida, USA.
  • Litzow MR; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Shallis RM; Section of Hematology, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
  • Patel A; Section of Hematology and Oncology, Department of Medicine, University of Chicago, Chicago, Illinois, USA.
  • Saliba AN; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Burkart M; Robert H. Lurie Comprehensive Cancer Center, Northwestern Hospital, Chicago, Illinois, USA.
  • Bewersdorf JP; Division of Hematologic Malignancies, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Stahl M; Section of Hematology and Oncology, Department of Medicine, University of Chicago, Chicago, Illinois, USA.
  • De Camargo Correia GS; Division of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, Florida, USA.
  • Guru Murthy GS; Department of Hematology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • Abaza Y; Robert H. Lurie Comprehensive Cancer Center, Northwestern Hospital, Chicago, Illinois, USA.
  • Duvall A; Section of Hematology and Oncology, Department of Medicine, University of Chicago, Chicago, Illinois, USA.
  • Bradshaw D; Division of Hematology and Medical Oncology, Georgia Cancer Center, Augusta, Georgia, USA.
  • Kota V; Division of Hematology and Medical Oncology, Georgia Cancer Center, Augusta, Georgia, USA.
  • Dinner S; Robert H. Lurie Comprehensive Cancer Center, Northwestern Hospital, Chicago, Illinois, USA.
  • Goldberg AD; Division of Hematologic Malignancies, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Palmisiano N; Division of Hematology and Oncology, Jefferson University Hospital, Philadelphia, Pennsylvania, USA.
  • Al Kali A; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Atallah E; Division of Hematology and Medical Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Cancer ; 129(6): 934-945, 2023 03 15.
Article en En | MEDLINE | ID: mdl-36545710
BACKGROUND: Although the clinical outcomes of patients with TP53-mutated acute myeloid leukemia (AML) are dismal, subsets of patients eligible for curative-intent therapies may fare better. Because racial disparities are known to affect outcome in hematologic malignancies, the authors sought to explore disparities among patients with TP53-mutated AML. METHODS: A multicenter, retrospective study was conducted in a cohort of 340 patients who had TP53-mutated AML (275 non-Hispanic White [NHW] and 65 non-Hispanic Black [NHB]) to analyze differences in treatment and outcome among NHW and NHB patients. RESULTS: The median patient age was comparable between NHW and NHB patients (p = .76). A higher proportion of NHB patients had therapy-related AML (31% vs. 20%; p = .08) and had co-mutations (74% vs. 61%; p = .06). A higher proportion of NHW patients received intensive chemotherapy compared with NHB patients (47% vs. 31%; p = .02). Conversely, a higher proportion of NHB patients received low-intensity chemotherapy (9% vs. 5.5%; p = .02) or best supportive care (22% vs. 7%; p < .001). The complete response rate (including complete responses with or without complete count recovery) was 31% versus 24.5% (p = .39) in NHW and NHB patients, respectively. Only 5% of NHB patients received allogeneic stem cell transplantation compared with 15.5% of NHW patients (p = .02). The proportion of patients who were event-free (18.5% vs. 8.5%; p = .49) or who remained alive (24.9% vs. 8.3%; p = .13) at 18 months was numerically higher in NHW versus NHB patients, respectively, but was not statistically significant. CONCLUSIONS: The current study highlights disparities between NHW and NHB patients with TP53-mutated AML. Efforts are warranted to eliminate treatment disparities in minority populations.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas / Disparidades en Atención de Salud Tipo de estudio: Clinical_trials / Observational_studies Límite: Humans Idioma: En Revista: Cancer Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas / Disparidades en Atención de Salud Tipo de estudio: Clinical_trials / Observational_studies Límite: Humans Idioma: En Revista: Cancer Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos