Donor Types and Outcomes of Transplantation in Myelofibrosis: A CIBMTR Study.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
25 Jun 2024
Historique:
accepted: 13 06 2024
received: 22 04 2024
revised: 13 06 2024
medline: 25 6 2024
pubmed: 25 6 2024
entrez: 25 6 2024
Statut: aheadofprint

Résumé

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.

Identifiants

pubmed: 38916866
pii: 516713
doi: 10.1182/bloodadvances.2024013451
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Society of Hematology.

Auteurs

Tania Jain (T)

Johns Hopkins University, Baltimore, Maryland, United States.

Noel Estrada-Merly (N)

CIBMTR, Milwaukee, Wisconsin, United States.

M Queralt Salas (MQ)

Hospital Clinic of Barcelona, Barcelona, Spain.

Soyoung Kim (S)

Medical College of Wisconsin, Milwaukee,, Wisconsin, United States.

Jakob D DeVos (JD)

Medical College of Wisconsin, Milwaukee, Wisconsin, United States.

Min Chen (M)

MCW, Milwaukee, Wisconsin, United States.

Xi Fang (X)

Medical College of Wisconsin, Milwaukee, Wisconsin, United States.

Rajat Kumar (R)

Princess Margaret Cancer Centre, Toronto, Canada.

Marcio Andrade-Campos (M)

Hospital del Mar, Barcelona, Spain.

Hany Elmariah (H)

Moffitt Cancer Center, Tampa, Florida, United States.

Vaibhav Agrawal (V)

City of Hope National Medical Center, Duarte, California, United States.

Mahmoud Aljurf (M)

King Faisal Specialist Hospital, Riyadh, Saudi Arabia.

Ulrike Bacher (U)

University Hospital Inselspital, Bern, Switzerland.

Talha Badar (T)

Mayo Clinic, Jacksonville, Florida, United States.

Sherif M Badawy (SM)

Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University, Chicago, Illinois, United States.

Karen Kuhn Ballen (KK)

University of Virginia, Charlottesville, Virginia, United States.

Amer Beitinjaneh (A)

University of Miami Health System, Miami, Florida, United States.

Vijaya R Bhatt (VR)

University of Nebraska Medical Center, Omaha, Nebraska, United States.

Christopher N Bredeson (CN)

The Ottawa Hospital / University of Ottawa, Ottawa, Canada.

Zachariah DeFilipp (Z)

Massachusetts General Hospital, Boston, Massachusetts, United States.

Bhagirathbhai Dholaria (B)

Vanderbilt University Medical Center, Nashville, Tennessee, United States.

Nosha Farhadfar (N)

Sarah Cannon Transplant & Cellular Therapy Program at Methodist Hospital, San Antonio, Texas, United States.

Shatha Farhan (S)

Henry Ford Healthsystem, detroit, Michigan, United States.

Arpita Gandhi (A)

Oregon Health & Science University, Portland, Oregon, United States.

Siddhartha Ganguly (S)

Houston Methodist Hospital, Houston, Texas, United States.

Usama Gergis (U)

Thomas Jefferson University, Philadelphia, Pennsylvania, United States.

Michael R Grunwald (MR)

Levine Cancer Institute, Atrium Health, Charlotte, North Carolina, United States.

Nada Hamad (N)

St Vincent's Hospital Sydney, Darlinghurst, Australia.

Betty K Hamilton (BK)

Cleveland Clinic, Cleveland, Ohio, United States.

Yoshihiro Inamoto (Y)

Fujita Health University School of Medicine, Toyoake, Japan.

Madiha Iqbal (M)

Mayo Clinic Florida, Jacksonville, Florida, United States.

Omer Jamy (O)

University of Alabama at Birmingham, Birmingham, Alabama, United States.

Mark Juckett (M)

University of Minnesota, Minneapolis, Minnesota, United States.

Mohamed A Kharfan-Dabaja (MA)

Mayo Clinic, Jacksonville, Florida, United States.

Maxwell M Krem (MM)

Kansas City VA Medical Center, Independence, Missouri, United States.

Deepesh P Lad (DP)

Leukemia/ BMT Program of BC, Vancouver, British Columbia, Canada.

Jane L Liesveld (JL)

University of Rochester Medical Center, Rochester, New York, United States.

Monzr M Al Malki (MM)

City of Hope National Medical Center, Duarte, California, United States.

Adriana K Malone (AK)

Icahn School of Medicine at Mount Sinai, New York, New York, United States.

Hemant S Murthy (HS)

Mayo Clinic Florida, Jacksonville, Florida, United States.

Guillermo Ortí (G)

University Hospital Vall d'Hebron, Barcelona, Spain.

Sagar S Patel (SS)

Huntsman Cancer Institute, Salt Lake City, Utah, United States.

Attaphol Pawarode (A)

University of Michigan, Ann Arbor, Michigan, United States.

Miguel-Angel Perales (MA)

Memorial Sloan Kettering Cancer Center, New York, New York, United States.

Marjolein W M van der Poel (MWM)

Maastricht University Medical Center, Maastricht, Netherlands.

Olle Ringden (O)

Karolinska Institutet, Huddinge, Sweden.

David A Rizzieri (DA)

Novant Health Cancer Institute, Charlotte, North Carolina, United States.

Alicia Rovo (A)

INSELSPITAL, Bern University Hospital, BERN, Switzerland.

Bipin N Savani (BN)

Vanderbilt University Medical Center, Nashville, Tennessee, United States.

Mary Lynn Savoie (ML)

Tom Baker Cancer Centre/University of Calgary, Calgary, Canada.

Sachiko Seo (S)

Tokyo Women's Medical University, Tokyo, Japan.

Melhem M Solh (MM)

The Blood and Marrow Transplant Program at Northside Hospital, Atlanta, Georgia, United States.

Celalettin Ustun (C)

Rush University, Chicago, Illinois, United States.

Leo F Verdonck (LF)

Isala Clinics, Zwolle, Netherlands.

John R Wingard (JR)

University of Florida College of Medicine, Gainesville, Florida, United States.

Baldeep Wirk (B)

Virginia Commonwealth University Medical Center, Richmond, Virginia, United States.

Nelli Bejanyan (N)

Moffitt Cancer Center, Tampa, Florida, United States.

Richard J Jones (RJ)

Sidney Kimmel Comprhehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, United States.

Taiga Nishihori (T)

Moffitt Cancer Center, Tampa, Florida, United States.

Betul Oran (B)

University of Texas, MD Anderson Cancer Center, Houston, Texas, United States.

Ryotaro Nakamura (R)

City of Hope National Medical Center, Duarte, California, United States.

Bart L Scott (BL)

Fred Hutchinson Cancer Research Center, Seattle, Washington, United States.

Wael Saber (W)

Division of Hematology Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin, United States.

Vikas Gupta (V)

The Princess Margaret Cancer Centre, Toronto, Canada.

Classifications MeSH