Haploidentical Donor Blood or Marrow Transplantation for Myelodysplastic/Myeloproliferative Overlap Neoplasms: Results from a North American Collaboration.


Journal

Research square
Titre abrégé: Res Sq
Pays: United States
ID NLM: 101768035

Informations de publication

Date de publication:
21 Mar 2023
Historique:
medline: 31 3 2023
entrez: 30 3 2023
pubmed: 31 3 2023
Statut: epublish

Résumé

Haploidentical donors offer a potentially readily available donor, especially for non-White patients, for blood or marrow transplantation (BMT). In this collaboration across North America, we retrospectively analyzed outcomes of first BMT using haploidentical donor and posttransplantation cyclophosphamide (PTCy) in MDS/MPN-overlap neoplasms (MDS/MPN), an otherwise incurable hematological neoplasm. We included 120 patients, 38% of non-White/Caucasian ethnicity, across 15 centers with median age at BMT 62.5 years. The median follow-up is 2.4 years. Graft failure was reported in 6% patients. At 3-years, nonrelapse mortality (NRM) was 25%, relapse 27%, grade 3-4 acute graft versus host disease (GVHD) 12%, chronic GVHD requiring systemic immunosuppression 14%, progression-free survival (PFS) 48% and overall survival (OS) 56%. On multivariable analysis, statistically significant associations included older age at BMT (per decade increment) with NRM (sdHR 3.28, 95%CI 1.30-8.25), PFS (HR 1.98, 95% 1.13-3.45) and OS (HR 2.01, 95% CI 1.11-3.63), presence of mutation in EZH2/RUNX1/SETBP1 with relapse (sdHR 2.61, 95%CI 1.06-6.44), and splenomegaly at BMT/prior splenectomy with OS (HR 2.20, 95%CI 1.04-4.65). Haploidentical donors are a viable option for BMT in MDS/MPN, especially for those disproportionately represented in the unrelated donor registry. Disease-related factors including splenomegaly and high-risk mutations dominate outcomes following BMT.

Identifiants

pubmed: 36993719
doi: 10.21203/rs.3.rs-2691216/v1
pmc: PMC10055643
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NCI NIH HHS
ID : P01 CA225618
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA006973
Pays : United States

Commentaires et corrections

Type : UpdateIn

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Auteurs

Tania Jain (T)

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University.

Hua-Ling Tsai (HL)

The Johns Hopkins University.

Hany Elmariah (H)

H. Lee Moffitt Cancer Center and Research Institute.

Pankit Vachhani (P)

O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham.

Sarah Wall (S)

The Ohio State University.

Asad Bashey (A)

Northside Hospital.

Alla Keyzner (A)

Icahn School of Medicine at Mount Sinai.

Roni Tamari (R)

Adult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center.

Michael Grunwald (M)

Levine Cancer Institute, Atrium Health.

Sameem Abedin (S)

Medical College of Wisconsin.

Kalyan Nadiminti (K)

University of Wisconsin School of Medicine and Public Health.

Madiha Iqbal (M)

Mayo Clinic.

Auro Viswabandya (A)

Princess Margaret Cancer Centre.

Shannon McCurdy (S)

Hospital of the University of Pennsylvania.

Monzr Al Malki (MA)

City of Hope National Medical Center.

Ravi Varadhan (R)

Johns Hopkins University School of Medicine.

Vikas Gupta (V)

Princess Margaret Hospital.

Richard John Jones (RJ)

Sidney Kimmel Comprehensive Cancer Center.

Salman Otoukesh (S)

City of Hope.

Classifications MeSH