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Racial, ethnic, and socioeconomic diversity and outcomes of patients with graft-versus-host disease: a CIBMTR analysis.
Farhadfar, Nosha; Rashid, Nahid; Chen, Karen; DeVos, Jakob; Wang, Tao; Ballen, Karen; Beitinjaneh, Amer; Bhatt, Vijaya Raj; Hamilton, Betty K; Hematti, Peiman; Gadalla, Shahinaz M; Solomon, Scott R; El Jurdi, Najla; Lee, Catherine J; MacMillan, Margaret L; Rangarajan, Hemalatha G; Schoemans, Hélène; Sharma, Akshay; Spellman, Stephen R; Wingard, John R; Lee, Stephanie J.
Afiliação
  • Farhadfar N; Sarah Cannon Transplant and Cellular Therapy Program at Methodist Hospital, San Antonio, TX.
  • Rashid N; Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
  • Chen K; Department of Bone Marrow Transplant, Southern California Permanente Medical Group, Duarte, CA.
  • DeVos J; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI.
  • Wang T; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI.
  • Ballen K; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI.
  • Beitinjaneh A; Division of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, WI.
  • Bhatt VR; Division of Hematology and Oncology, University of Virginia Health System, Charlottesville, VA.
  • Hamilton BK; Division of Transplantation and Cellular Therapy, University of Miami Hospital and Clinics, Sylvester Comprehensive Cancer Center, Miami, FL.
  • Hematti P; The Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE.
  • Gadalla SM; Blood and Marrow Transplant Program, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH.
  • Solomon SR; Division of Hematology/Oncology, BMT & Cellular Therapy Program, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
  • El Jurdi N; Division of Cancer Epidemiology and Genetics, Clinical Genetics Branch, National Cancer Institute, National Institutes of Health, Rockville, MD.
  • Lee CJ; Blood and Marrow Transplant Program, Northside Hospital Cancer Institute, Atlanta, GA.
  • MacMillan ML; Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, MN.
  • Rangarajan HG; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Schoemans H; Blood and Marrow Transplant Program, Department of Pediatrics, University of Minnesota, Minneapolis, MN.
  • Sharma A; Department of Pediatric Hematology, Oncology & Blood and Marrow Transplant, Nationwide Children's Hospital, Columbus, OH.
  • Spellman SR; Department of Hematology, University Hospitals Leuven, Leuven, Belgium.
  • Wingard JR; Department of Public Health and Primary Care, ACCENT VV, KU Leuven, University of Leuven, Leuven, Belgium.
  • Lee SJ; Department of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, TN.
Blood Adv ; 8(18): 4963-4976, 2024 Sep 24.
Article em En | MEDLINE | ID: mdl-38776400
ABSTRACT
ABSTRACT Socioeconomic status (SES) and race/ethnicity have been associated with the outcomes of allogeneic hematopoietic stem cell transplantation (allo-HCT). Certain aspects of graft-versus-host disease (GVHD) management, such as the need for long-term care, prolonged immunosuppressive treatment, and close follow-up for complications, may exacerbate disparities. Adults (≥18 years) reported to the Center for International Blood and Marrow Transplant Research who underwent a first allo-HCT for acute leukemia, myelodysplastic syndrome, or myeloproliferative neoplasm between 2008 and 2018 were included. End points for those developing GVHD included overall survival (OS), transplant-related mortality (TRM), and disease relapse. Models were adjusted for patient- and transplant-related variables. A 2-sided P value < .01 was considered significant. Among the 14 825 allo-HCT recipients, 6259 (42.2%) and 6675 (45.0%) patients developed acute GVHD (aGVHD) and chronic GVHD (cGVHD), respectively. Among patients with aGVHD, non-Hispanic Black patients had increased TRM and overall mortality compared with non-Hispanic White patients; this association disappeared when severity of aGVHD was included in the model. Lower SES was associated with increased risk of disease relapse but not OS or TRM. In patients who developed cGVHD, race and ethnicity were not associated with OS, TRM, or disease relapse. However, the highest quartile of annual household income (≥$80 000) had improved OS and reduced TRM compared with the lowest quartile, after adjusting for race and ethnicity. In summary, race/ethnicity and SES are associated with outcomes after GVHD. Optimizing the health care resources available to low SES patients and strategies to minimize the risk of severe GVHD in non-Hispanic Black patients may improve long-term outcomes.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Adv Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Adv Ano de publicação: 2024 Tipo de documento: Article