Decitabine-based treatment strategy improved the outcome of HSCT in JMML: a retrospective cohort study.
Humans
Decitabine
/ therapeutic use
Hematopoietic Stem Cell Transplantation
/ adverse effects
Retrospective Studies
Female
Male
Child, Preschool
Leukemia, Myelomonocytic, Juvenile
/ therapy
Treatment Outcome
Infant
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Child
Vidarabine
/ analogs & derivatives
Cytarabine
/ therapeutic use
FLAG protocol
decitabine
hematopoietic stem cell transplantation (HSCT)
hypomethylating agents
juvenile myelomonocytic leukemia (JMML)
maintenance treatment
pretransplant therapy
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2024
2024
Historique:
received:
01
05
2024
accepted:
01
08
2024
medline:
10
9
2024
pubmed:
10
9
2024
entrez:
10
9
2024
Statut:
epublish
Résumé
Pre-HSCT disease control, suboptimal long-term prognosis, and a high recurrence incidence (RI) continue to pose significant challenges for hematopoietic stem cell transplantation (HSCT) in juvenile myelomonocytic leukemia (JMML) patients. This retrospective cohort study assessed the effectiveness of a decitabine (DAC)-based protocol in JMML patients undergoing HSCT. The pre-HSCT treatment includes initial and bridging treatment. The efficacy of DAC monotherapy versus DAC combined with cytotoxic chemotherapy(C-DAC) as initial treatment was compared, followed by DAC plus FLAG (fludarabine, cytarabine, and GCSF) as bridging treatment. The HSCT regimens were based on DAC, fludarabine, and busulfan. Post-HSCT, low-dose DAC was used as maintenance therapy. The study endpoints focused on pretransplantation simplified clinical response and post-HSCT survival. There were 109 patients, including 45 receiving DAC monotherapy and 64 undergoing C-DAC treatment. 106 patients completed bridging treatment. All patients were administered planned HSCT regimens and post-HSCT treatment. The initial treatment resulted in 88.1% of patients achieving clinical remission without a significant difference between the DAC and C-DAC groups ( Implementing a DAC-based administration strategy throughout the pre-HSCT period, during HSCT regimens, and in post-HSCT maintenance significantly reduced relapse and improved survival in JMML patients. Both DAC monotherapy and the DAC plus FLAG protocol proved effective as pre-HSCT treatments.
Identifiants
pubmed: 39253078
doi: 10.3389/fimmu.2024.1426640
pmc: PMC11381242
doi:
Substances chimiques
Decitabine
776B62CQ27
Vidarabine
FA2DM6879K
fludarabine
P2K93U8740
Cytarabine
04079A1RDZ
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1426640Informations de copyright
Copyright © 2024 Peng, Gao, Huang, He, Tang, Zong, Pei, Pei, Ge, Liu, Yue, Zhou, Li, Yue, Chen, Chen, Wu, Feng and Li.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.