Similar transplant outcomes between haploidentical and unrelated donors after reduced-intensity conditioning with busulfan, fludarabine, and anti-thymocyte globulin in patients with acute leukemia or myelodysplastic syndrome.

Anti-thymocyte globulin HLA-matched unrelated donor Haploidentical stem cell transplantation Reduced-intensity conditioning

Journal

Blood research
ISSN: 2287-979X
Titre abrégé: Blood Res
Pays: Korea (South)
ID NLM: 101605247

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 27 07 2019
revised: 12 12 2019
accepted: 03 02 2020
entrez: 10 4 2020
pubmed: 10 4 2020
medline: 10 4 2020
Statut: ppublish

Résumé

Although T-cell-replete hematopoietic cell transplantation (HCT) from haploidentical donors (HIDs) using anti-thymocyte globulin (ATG) has shown promising outcomes, previous studies often adopted heterogenous graft sources and conditioning. We retrospectively compared HCT outcomes from 62 HIDs, 36 partially-matched unrelated donors (PUDs), and 55 matched unrelated donors (MUDs) in patients with acute leukemia or myelodysplastic syndrome using the same graft source of peripheral blood and a reduced intensity conditioning of busulfan, fludarabine, and ATG. The estimates of 3-yr disease-free survival (DFS) and overall survival (OS) rates were not significantly different among the MUD, HID, and PUD groups, at 46%, "41%, and 36%" for the DFS rate ( T-cell replete HCT from HIDs using an ATG-containing reduced intensity conditioning regimen may be a reasonable option in the absence of matched related donors in patients with acute leukemia or myelodysplastic syndrome.

Sections du résumé

BACKGROUND BACKGROUND
Although T-cell-replete hematopoietic cell transplantation (HCT) from haploidentical donors (HIDs) using anti-thymocyte globulin (ATG) has shown promising outcomes, previous studies often adopted heterogenous graft sources and conditioning.
METHODS METHODS
We retrospectively compared HCT outcomes from 62 HIDs, 36 partially-matched unrelated donors (PUDs), and 55 matched unrelated donors (MUDs) in patients with acute leukemia or myelodysplastic syndrome using the same graft source of peripheral blood and a reduced intensity conditioning of busulfan, fludarabine, and ATG.
RESULTS RESULTS
The estimates of 3-yr disease-free survival (DFS) and overall survival (OS) rates were not significantly different among the MUD, HID, and PUD groups, at 46%, "41%, and 36%" for the DFS rate (
CONCLUSION CONCLUSIONS
T-cell replete HCT from HIDs using an ATG-containing reduced intensity conditioning regimen may be a reasonable option in the absence of matched related donors in patients with acute leukemia or myelodysplastic syndrome.

Identifiants

pubmed: 32269972
doi: 10.5045/br.2020.55.1.27
pmc: PMC7106115
doi:

Types de publication

Journal Article

Langues

eng

Pagination

27-34

Informations de copyright

© 2020 Korean Society of Hematology.

Déclaration de conflit d'intérêts

Authors' Disclosures of Potential Conflicts of Interest: No potential conflicts of interest relevant to this article were reported.

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Auteurs

Mihong Choi (M)

Division of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.

Ja Yoon Heo (JY)

Division of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.

Dong-Yeop Shin (DY)

Division of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Center for Medical Innovation, Biomedical Research Institute, Seoul National University Hospital, Seoul, Korea.
Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.

Ji Yun Lee (JY)

Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.

Youngil Koh (Y)

Division of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Center for Medical Innovation, Biomedical Research Institute, Seoul National University Hospital, Seoul, Korea.
Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.

Junshik Hong (J)

Division of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Center for Medical Innovation, Biomedical Research Institute, Seoul National University Hospital, Seoul, Korea.
Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.

Inho Kim (I)

Division of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.

Sung-Soo Yoon (SS)

Division of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Center for Medical Innovation, Biomedical Research Institute, Seoul National University Hospital, Seoul, Korea.
Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.

Jeong-Ok Lee (JO)

Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.

Soo-Mee Bang (SM)

Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.

Classifications MeSH