Mutation clonal burden and allogeneic hematopoietic cell transplantation outcomes in acute myeloid leukemia and myelodysplastic syndromes.
Adolescent
Adult
Aged
Female
Hematopoietic Stem Cell Transplantation
/ methods
High-Throughput Nucleotide Sequencing
/ methods
Humans
Leukemia, Myeloid, Acute
/ genetics
Male
Middle Aged
Mutation
Myelodysplastic Syndromes
/ genetics
Prognosis
Transplantation Conditioning
/ methods
Transplantation, Homologous
/ methods
Young Adult
Journal
Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
27
07
2018
accepted:
04
01
2019
revised:
20
12
2018
pubmed:
19
1
2019
medline:
13
8
2020
entrez:
19
1
2019
Statut:
ppublish
Résumé
Next generation sequencing (NGS) has become an important tool to inform disease risk for myeloid malignancies, however data remains conflicting regarding the significance of individual mutations. We performed targeted NGS on 112 patients with AML, and 80 with MDS, who underwent allogeneic hematopoietic cell transplantation. The most common mutations in AML were TET2 (14.7%), FLT3 (12.9%), DNMT3A (12.1%), and RUNX1 (7.8%). Complex cytogenetics (HR 2.82, P = .017) and disease status (<CR) (HR 2.58, P < .001) was significantly associated with worse RFS. No individual mutation, nor variant allelic frequency (VAF), was found to be prognostic, except mutations in the RNA-splicing pathway, (HR 2.09, P = .023). Within the MDS cohort, most common mutations were ASXL1 (12.5%), SRSF2 (12%), TET2 (8.8%), and TP53 (8.8%). Complex cytogenetics (HR 5.01, P < .001), and presence of U2AF1 (HR 3.60, P = .019), was associated with worse RFS. Analysis of VAF found that TP53 and EZH2 mutations with allelic frequencies of >33% were associated with poor RFS (HR 3.57, P = .017; and HR 6.57, P = .003; respectively). Molecular profiling is increasingly important in the care of patients with AML and MDS. Further studies are needed to understand the molecular complexities, including the significance of clonal burden, to better inform care decisions.
Identifiants
pubmed: 30655603
doi: 10.1038/s41409-019-0444-1
pii: 10.1038/s41409-019-0444-1
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM