Natural killer cell cytotoxicity is a predictor of outcome for patients with high risk myelodysplastic syndrome and oligoblastic acute myeloid leukemia treated with azacytidine.
Aged
Aged, 80 and over
Azacitidine
/ administration & dosage
Biomarkers
Cell Line, Tumor
Cytotoxicity, Immunologic
Female
Humans
Killer Cells, Natural
/ immunology
Leukemia, Myeloid, Acute
/ diagnosis
Lymphocyte Subsets
/ immunology
Male
Middle Aged
Myelodysplastic Syndromes
/ diagnosis
Prognosis
ROC Curve
NK-cytotoxicity
Natural killer cell
acute myeloid leukemia
azacytidine
myelodysplastic syndrome
Journal
Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422
Informations de publication
Date de publication:
10 2019
10 2019
Historique:
pubmed:
6
4
2019
medline:
18
8
2020
entrez:
6
4
2019
Statut:
ppublish
Résumé
The aim of the present study was to identify biomarkers predictive of the outcome of patients with high-risk myelodysplastic syndrome and oligoblastic acute myeloid leukemia (AML) treated with 5-azacytidine (AZA). We prospectively examined the association between NK-cytotoxic activity, myeloid-derived suppressor cells (MDSCs), and T-regulatory cells (Tregs) on the overall survival (OS) of patients. Patients with NK-cytotoxicity above a critical threshold had a longer duration of response and survived longer than patients with severe impairment of NK-cytotoxicity. The numbers of MDSCs, and Tregs in the PB of patients after a short exposure to AZA were not different from normal donors. In conclusion, the results of our study suggest that the therapeutic activity of AZA is at least partly mediated by an immunomodulatory effect. To our knowledge, this is the first study reported so far, that shows a positive correlation between NK cytotoxicity and OS of AZA-treated patients.
Identifiants
pubmed: 30947589
doi: 10.1080/10428194.2019.1581935
doi:
Substances chimiques
Biomarkers
0
Azacitidine
M801H13NRU
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2457-2463Commentaires et corrections
Type : CommentIn