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Donor Types and Outcomes of Transplantation in Myelofibrosis: A CIBMTR Study.
Jain, Tania; Estrada-Merly, Noel; Salas, M Queralt; Kim, Soyoung; DeVos, Jakob D; Chen, Min; Fang, Xi; Kumar, Rajat; Andrade-Campos, Marcio; Elmariah, Hany; Agrawal, Vaibhav; Aljurf, Mahmoud; Bacher, Ulrike; Badar, Talha; Badawy, Sherif M; Ballen, Karen Kuhn; Beitinjaneh, Amer; Bhatt, Vijaya R; Bredeson, Christopher N; DeFilipp, Zachariah; Dholaria, Bhagirathbhai; Farhadfar, Nosha; Farhan, Shatha; Gandhi, Arpita; Ganguly, Siddhartha; Gergis, Usama; Grunwald, Michael R; Hamad, Nada; Hamilton, Betty K; Inamoto, Yoshihiro; Iqbal, Madiha; Jamy, Omer; Juckett, Mark; Kharfan-Dabaja, Mohamed A; Krem, Maxwell M; Lad, Deepesh P; Liesveld, Jane L; Al Malki, Monzr M; Malone, Adriana K; Murthy, Hemant S; Ortí, Guillermo; Patel, Sagar S; Pawarode, Attaphol; Perales, Miguel-Angel; van der Poel, Marjolein W M; Ringden, Olle; Rizzieri, David A; Rovo, Alicia; Savani, Bipin N; Savoie, Mary Lynn.
Afiliação
  • Jain T; Johns Hopkins University, Baltimore, Maryland, United States.
  • Estrada-Merly N; CIBMTR, Milwaukee, Wisconsin, United States.
  • Salas MQ; Hospital Clinic of Barcelona, Barcelona, Spain.
  • Kim S; Medical College of Wisconsin, Milwaukee,, Wisconsin, United States.
  • DeVos JD; Medical College of Wisconsin, Milwaukee, Wisconsin, United States.
  • Chen M; MCW, Milwaukee, Wisconsin, United States.
  • Fang X; Medical College of Wisconsin, Milwaukee, Wisconsin, United States.
  • Kumar R; Princess Margaret Cancer Centre, Toronto, Canada.
  • Andrade-Campos M; Hospital del Mar, Barcelona, Spain.
  • Elmariah H; Moffitt Cancer Center, Tampa, Florida, United States.
  • Agrawal V; City of Hope National Medical Center, Duarte, California, United States.
  • Aljurf M; King Faisal Specialist Hospital, Riyadh, Saudi Arabia.
  • Bacher U; University Hospital Inselspital, Bern, Switzerland.
  • Badar T; Mayo Clinic, Jacksonville, Florida, United States.
  • Badawy SM; Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University, Chicago, Illinois, 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.
  • Bredeson CN; The Ottawa Hospital / University of Ottawa, Ottawa, Canada.
  • DeFilipp Z; Massachusetts General Hospital, Boston, Massachusetts, United States.
  • Dholaria B; Vanderbilt University Medical Center, Nashville, Tennessee, United States.
  • Farhadfar N; Sarah Cannon Transplant & Cellular Therapy Program at Methodist Hospital, San Antonio, Texas, United States.
  • Farhan S; Henry Ford Healthsystem, detroit, Michigan, United States.
  • Gandhi A; Oregon Health & Science University, Portland, Oregon, United States.
  • Ganguly S; Houston Methodist Hospital, Houston, Texas, United States.
  • Gergis U; Thomas Jefferson University, Philadelphia, Pennsylvania, United States.
  • Grunwald MR; Levine Cancer Institute, Atrium Health, Charlotte, North Carolina, United States.
  • Hamad N; St Vincent's Hospital Sydney, Darlinghurst, Australia.
  • Hamilton BK; Cleveland Clinic, Cleveland, Ohio, United States.
  • Inamoto Y; Fujita Health University School of Medicine, Toyoake, Japan.
  • Iqbal M; Mayo Clinic Florida, Jacksonville, Florida, United States.
  • Jamy O; University of Alabama at Birmingham, Birmingham, Alabama, United States.
  • Juckett M; University of Minnesota, Minneapolis, Minnesota, United States.
  • Kharfan-Dabaja MA; Mayo Clinic, Jacksonville, Florida, United States.
  • Krem MM; Kansas City VA Medical Center, Independence, Missouri, United States.
  • Lad DP; Leukemia/ BMT Program of BC, Vancouver, British Columbia, Canada.
  • Liesveld JL; University of Rochester Medical Center, Rochester, New York, United States.
  • Al Malki MM; City of Hope National Medical Center, Duarte, California, United States.
  • Malone AK; Icahn School of Medicine at Mount Sinai, New York, New York, United States.
  • Murthy HS; Mayo Clinic Florida, Jacksonville, Florida, United States.
  • Ortí G; University Hospital Vall d'Hebron, Barcelona, Spain.
  • Patel SS; Huntsman Cancer Institute, Salt Lake City, Utah, United States.
  • Pawarode A; University of Michigan, Ann Arbor, Michigan, United States.
  • Perales MA; Memorial Sloan Kettering Cancer Center, New York, New York, United States.
  • van der Poel MWM; Maastricht University Medical Center, Maastricht, Netherlands.
  • Ringden O; Karolinska Institutet, Huddinge, Sweden.
  • Rizzieri DA; Novant Health Cancer Institute, Charlotte, North Carolina, United States.
  • Rovo A; INSELSPITAL, Bern University Hospital, BERN, Switzerland.
  • Savani BN; Vanderbilt University Medical Center, Nashville, Tennessee, United States.
  • Savoie ML; Tom Baker Cancer Centre/University of Calgary, Calgary, Canada.
Blood Adv ; 2024 Jun 25.
Article em En | MEDLINE | ID: mdl-38916866
ABSTRACT
We aim to evaluate impact of donor types on outcomes of hematopoietic cell transplantation (HCT) in myelofibrosis, using CIBMTR registry data for HCTs done between 2013 and 2019. In all 1597 undergoing HCT for myelofibrosis, the use of haploidentical donors increased from 3% in 2013 to 19% in 2019. In study eligible, 1032 patients who received peripheral blood grafts for chronic phase myelofibrosis, 38% recipients of haploidentical-HCT were of non-White/Caucasian ethnicity. Matched sibling donor (MSD)-HCTs were independently associated with superior overall survival (OS) in the first 3 months [reference MSD, haploidentical HR 5.80 (95% CI 2.52-13.35), matched unrelated HR 4.50 (95% CI 2.24-9.03), and mismatched unrelated HR 5.13 (95% CI 1.44-18.31), P<0.001]. This difference in OS aligns with lower graft failure with MSD [haploidentical HR 6.11 (95%CI 2.98-12.54), matched unrelated HR 2.33 (95%CI 1.20-4.51), mismatched unrelated HR 1.82 (95%CI 0.58-5.72). There was no significant difference in OS among haploidentical, matched unrelated, and mismatched unrelated donor HCTs in the first 3 months. Donor type was not associated with differences in OS beyond 3 months post-HCT, relapse, disease-free survival or OS among patients who underwent HCT within 24 months of diagnosis. Patients who experienced graft failure had more advanced disease and commonly used nonmyeloablative conditioning. While MSDs remain a superior donor option due to improved engraftment, there is no significant difference in HCT outcomes from haploidentical and matched unrelated donors. These results establish haploidentical-HCT with posttransplantation cyclophosphamide as a viable option in myelofibrosis, especially for ethnic minorities underrepresented in the donor registries.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Blood Adv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Blood Adv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos