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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 D; Wang, Tao; Ballen, Karen Kuhn; Beitinjaneh, Amer; Bhatt, Vijaya R; 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 M; Sharma, Akshay; Spellman, Stephen R; Wingard, John R; Lee, Stephanie J.
Afiliação
  • Farhadfar N; Sarah Cannon Transplant & Cellular Program at Methodist Hospital, United States.
  • Rashid N; City of Hope National Medical Center, United States.
  • Chen K; Medical College of Wisconsin, Milwaukee, Wisconsin, United States.
  • DeVos JD; Medical College of Wisconsin, Milwaukee, Wisconsin, United States.
  • Wang T; Medical College of Wisconsin, Milwaukee, Wisconsin, United States.
  • Ballen KK; University of Virginia, Charlottesville, Virginia, United States.
  • Beitinjaneh A; University of Miami Health System, Miami, Florida, United States.
  • Bhatt VR; University of Nebraska Medical Center, Omaha, Nebraska, United States.
  • Hamilton BK; Cleveland Clinic, Cleveland, Ohio, United States.
  • Hematti P; Medical College of Wisconsin, Madison, Wisconsin, United States.
  • Gadalla SM; National Cancer Institute, Rockville, Maryland, United States.
  • Solomon SR; BMT, Leukemia and Cellular Immunotherapy Programs, Northside Hospital Cancer Institute, Atlanta, Georgia, United States.
  • El Jurdi N; University of Minnesota, Minneapolis, Minnesota, United States.
  • Lee CJ; Fred Hutchinson Cancer Center, Seattle, Washington, United States.
  • MacMillan ML; University of Minnesota, Minneapolis, Minnesota, United States.
  • Rangarajan HG; Nationwide Childrens Hosptial, Columbus, Ohio, United States.
  • Schoemans HM; University Hospitals Leuven, Leuven, Belgium.
  • Sharma A; St Jude Children's Research Hospital, Memphis, Tennessee, United States.
  • Spellman SR; CIBMTR® (Center for International Blood and Marrow Transplant Research), NMDP, Minneapolis, Minnesota, United States.
  • Wingard JR; University of Florida College of Medicine, Gainesville, Florida, United States.
  • Lee SJ; CIBMTR® (Center for International Blood and Marrow Transplant Research), Medical College of Wisconsin, United States.
Blood Adv ; 2024 May 22.
Article em En | MEDLINE | ID: mdl-38776400
ABSTRACT
Socioeconomic status (SES) and race/ethnicity have been associated with outcomes of allogeneic hematopoietic cell transplantation (allo-HCT). Certain aspects of GVHD management such as the need for long term care, prolonged immunosuppressive treatment, and need for close follow up for complications may exacerbate disparities. Adults (≥ 18 years) reported to the Center for International Blood and Marrow Transplant Research (CIBMTR) who underwent a first alloHCT for acute leukemia, myelodysplastic syndrome, or myeloproliferative neoplasm between 2008 - 2018 were included. Endpoints 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 two-sided p-value < 0.01 was considered significant. Among the 14,825 allo-HCT recipients, 6,259 (42.2%) and 6,675 (45.0%) patients developed aGVHD and cGVHD, respectively. In patients with aGVHD, non-Hispanic Blacks had increased TRM (HR 1.50, 95% CI 1.24-1.83, p=0.0001) and overall mortality (HR 1.31, 1.14-1.50, p=0.0002) compared with non-Hispanic Whites, an association that disappeared when severity of aGVHD was included in the model. Lower SES was associated with increased risk of disease relapse (p=0.0016) but not OS or TRM. In patients who developed cGVHD, race and ethnicity were not associated with OS, TRM and disease relapse. However, the highest quartile of annual household income (≥ $80,000) had improved OS (HR 0.77, 0.69-0.85, p<0.0001) and reduced TRM (HR 0.86, 0.67-0.87, p<0.0001) compared with lowest quartile, adjusting for race and ethnicity. Race/ethnicity and SES are associated with outcomes after GVHD. Optimizing health care resources available to low SES patients and strategies to minimize the risk of severe GVHD in non-Hispanic Blacks may improve long-term outcomes.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article