RBC transfusion independence among lower risk MDS patients receiving hypomethylating agents: a population-level analysis.
Aged
Aged, 80 and over
Antimetabolites, Antineoplastic
/ pharmacology
Azacitidine
/ pharmacology
DNA Methylation
/ drug effects
Decitabine
/ pharmacology
Erythrocyte Transfusion
/ statistics & numerical data
Female
Humans
Kaplan-Meier Estimate
Male
Medicare
/ statistics & numerical data
Myelodysplastic Syndromes
/ blood
Retrospective Studies
SEER Program
/ statistics & numerical data
Severity of Illness Index
Treatment Outcome
United States
HMA
MDS
azacitdine
decitabine
transfusion
Journal
Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
pubmed:
7
6
2019
medline:
10
9
2020
entrez:
8
6
2019
Statut:
ppublish
Résumé
Most patients with lower risk myelodysplastic syndromes (LR-MDS) become red blood cell (RBC) transfusion dependent at some time during their disease course. Hypomethylating agents (HMAs) are frequently used in this setting; however, reported rates of in RBC transfusion independence (TI) achieved with HMA therapy vary significantly between studies. Here we study the real-life clinical effectiveness of HMA in inducing RBC TI in anemic LR-MDS patients using the Surveillance, Epidemiology and End Results (SEER)-Medicare database. We find that approximately 40% of LR-MDS patients who were receiving RBC transfusions and 33% who were dependent on RBC transfusions at HMA initiation ultimately achieved TI. The receipt of ≥3 transfusions in the 8-week period before HMA initiation was significantly associated with lower odds of achieving TI. Our study provides important population level estimates of clinical effectiveness of HMAs in LR-MDS.
Identifiants
pubmed: 31170846
doi: 10.1080/10428194.2019.1622700
doi:
Substances chimiques
Antimetabolites, Antineoplastic
0
Decitabine
776B62CQ27
Azacitidine
M801H13NRU
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
3181-3187Subventions
Organisme : NCI NIH HHS
ID : P30 CA016359
Pays : United States
Organisme : NCI NIH HHS
ID : N01PC35136
Pays : United States
Organisme : NCI NIH HHS
ID : N01PC35139
Pays : United States