Sorafenib maintenance after hematopoietic stem cell transplantation improves outcome of FLT3-ITD-mutated acute myeloid leukemia.


Journal

International journal of hematology
ISSN: 1865-3774
Titre abrégé: Int J Hematol
Pays: Japan
ID NLM: 9111627

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 19 04 2022
accepted: 20 07 2022
revised: 20 07 2022
pubmed: 10 8 2022
medline: 22 11 2022
entrez: 9 8 2022
Statut: ppublish

Résumé

In a retrospective analysis, 21 acute myeloid leukemia patients receiving single-agent sorafenib maintenance therapy in complete remission (CR) after hematopoietic stem cell transplantation (HSCT) were compared with a control group of 22 patients without maintenance. Sorafenib was initiated a median of 3 months (IQR: 2.3-3.5) after allogeneic HSCT with a median daily dosage of 400 mg (range: 200-800) orally, and lasted a median of 11.3 months (IQR: 3.3-24.4). No significant increase in graft versus host disease or toxicity was observed. Adverse events were reversible with dose adjustment or temporary discontinuation in 19/19 cases. With a median follow-up of 34.7 months (IQR: 16.9-79.5), sorafenib maintenance significantly improved cumulative incidence of relapse (p = 0.028) as well as overall survival (OS) (p = 0.016), especially in patients undergoing allogeneic HSCT in CR1 (p < 0.001). In conclusion, sorafenib maintenance after allogeneic HSCT is safe and may improve cumulative incidence of relapse and OS in FLT3-ITD-mutated AML.

Identifiants

pubmed: 35943684
doi: 10.1007/s12185-022-03427-4
pii: 10.1007/s12185-022-03427-4
pmc: PMC9668769
doi:

Substances chimiques

Sorafenib 9ZOQ3TZI87
Phenylurea Compounds 0
Niacinamide 25X51I8RD4
fms-Like Tyrosine Kinase 3 EC 2.7.10.1
FLT3 protein, human EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

883-891

Informations de copyright

© 2022. The Author(s).

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Auteurs

Semra Aydin (S)

Department of Oncology, Hematology, Immuno-Oncology and Rheumatology, University Hospital of Bonn, Venusberg-Campus 1, 53127, Bonn, Germany. Semra.Aydin@ukbonn.de.
Department of Oncology, Hematology, A.O.U. Città Della Salute e Della Scienza, Turin, Italy. Semra.Aydin@ukbonn.de.

Roberto Passera (R)

Department of Medical Sciences, A.O.U. Città Della Salute e Della Scienza, University of Torino, Turin, Italy.

Matilde Scaldaferri (M)

S.C. Clinical Pharmacology, A.O.U. Città Della Salute e Della Scienza, Turin, Italy.

Chiara Maria Dellacasa (CM)

Department of Oncology, SSD Stem Cell Transplant Center, A.O.U. Città Della Salute e Della Scienza, Turin, Italy.

Marco Poggiu (M)

S.C. Clinical Pharmacology, A.O.U. Città Della Salute e Della Scienza, Turin, Italy.

Francesco Cattel (F)

S.C. Clinical Pharmacology, A.O.U. Città Della Salute e Della Scienza, Turin, Italy.

Francesco Zallio (F)

Department of Hematology, SS Antonio & Biagio and C. Arrigo Hospital, Alessandria, Italy.

Lucia Brunello (L)

Department of Hematology, SS Antonio & Biagio and C. Arrigo Hospital, Alessandria, Italy.

Luisa Giaccone (L)

Department of Oncology, SSD Stem Cell Transplant Center, A.O.U. Città Della Salute e Della Scienza, Turin, Italy.

Irene Dogliotti (I)

Department of Oncology, SSD Stem Cell Transplant Center, A.O.U. Città Della Salute e Della Scienza, Turin, Italy.

Alessandro Busca (A)

Department of Oncology, SSD Stem Cell Transplant Center, A.O.U. Città Della Salute e Della Scienza, Turin, Italy.

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