Venetoclax in patients with acute myeloid leukemia refractory to hypomethylating agents-a multicenter historical prospective study.
Adult
Aged
Aged, 80 and over
Antimetabolites, Antineoplastic
/ administration & dosage
Antineoplastic Agents
/ therapeutic use
Azacitidine
/ administration & dosage
Bridged Bicyclo Compounds, Heterocyclic
/ therapeutic use
Chemotherapy-Induced Febrile Neutropenia
/ etiology
Decitabine
/ administration & dosage
Drug Administration Schedule
Drug Resistance, Neoplasm
/ drug effects
Female
Hematopoietic Stem Cell Transplantation
Humans
Leukemia, Myeloid, Acute
/ drug therapy
Male
Middle Aged
Prospective Studies
Remission Induction
Sulfonamides
/ therapeutic use
Survival Analysis
Transplantation, Homologous
Acute myeloid leukemia
Hypomethylating agents
Refractory
Venetoclax
Journal
Annals of hematology
ISSN: 1432-0584
Titre abrégé: Ann Hematol
Pays: Germany
ID NLM: 9107334
Informations de publication
Date de publication:
Aug 2019
Aug 2019
Historique:
received:
08
02
2019
accepted:
20
05
2019
pubmed:
13
6
2019
medline:
26
7
2019
entrez:
13
6
2019
Statut:
ppublish
Résumé
Patients with acute myeloid leukemia (AML) who progress after exposure to hypomethylating agents (HMA) have a dismal prognosis. We hypothesized that the addition of venetoclax, a BCL-2 inhibitor, to AML patients who previously failed HMA might overcome resistance. Adult patients (≥ 18 years) with AML were eligible if leukemia relapsed after, or was refractory to HMA. In general, in addition to venetoclax, patients continued HMA or other low-intensity therapies. Patients who previously underwent allogeneic hematopoietic cell transplantation (HCT) were also eligible. Data were analyzed in November 2018. Twenty-three patients were treated between October 2016 and October 2018 and were eligible for this study. Median age was 76 years and 6 patients had leukemia that relapsed post allogeneic HCT. None of the patients experienced tumor lysis syndrome and toxicities were as expected and manageable. Febrile neutropenia was the most common toxicity (78% of patients). Median hospitalization time was 13 days. Forty-three percent of the patients achieved CR/CRi. Overall survival (OS) was 74% at 6 months and median OS in patients who achieved remission was 10.8 months. Higher number of blasts in both bone marrow and peripheral blood was associated with lower chances of CR, while higher WBC, LDH, and bone marrow or peripheral blasts were associated with increased mortality rate. The addition of venetoclax to patients with HMA-refractory AML may result in a substantial anti-leukemic activity, specifically in those achieving complete remission. This should be further tested in a well-designed prospective trial.
Identifiants
pubmed: 31187237
doi: 10.1007/s00277-019-03719-6
pii: 10.1007/s00277-019-03719-6
doi:
Substances chimiques
Antimetabolites, Antineoplastic
0
Antineoplastic Agents
0
Bridged Bicyclo Compounds, Heterocyclic
0
Sulfonamides
0
Decitabine
776B62CQ27
Azacitidine
M801H13NRU
venetoclax
N54AIC43PW
Types de publication
Journal Article
Multicenter Study
Langues
eng