A phase II study of decitabine and gemtuzumab ozogamicin in newly diagnosed and relapsed acute myeloid leukemia and high-risk myelodysplastic syndrome.

Autor: Daver N; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Kantarjian H; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Ravandi F; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Estey E; Division of Hematology, University of Washington School of Medicine, Seattle, WA, USA., Wang X; Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Garcia-Manero G; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Jabbour E; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Konopleva M; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., O'Brien S; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Verstovsek S; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Kadia T; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Dinardo C; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Pierce S; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Huang X; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Pemmaraju N; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Diaz-Pines-Mateo M; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Cortes J; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Borthakur G; Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jazyk: angličtina
Zdroj: Leukemia [Leukemia] 2016 Feb; Vol. 30 (2), pp. 268-73. Date of Electronic Publication: 2015 Sep 14.
DOI: 10.1038/leu.2015.244
Abstrakt: Decitabine may open the chromatin structure of leukemia cells making them accessible to the calicheamicin epitope of gemtuzumab ozogamicin (GO). A total of 110 patients (median age 70 years; range 27-89 years) were treated with decitabine and GO in a trial designed on model-based futility to accommodate subject heterogeneity: group 1: relapsed/refractory acute myeloid leukemia (AML) with complete remission duration (CRD) <1 year (N=28, 25%); group 2: relapsed/refractory AML with CRD ⩾1 year (N=5, 5%); group 3: untreated AML unfit for intensive chemotherapy or untreated myelodysplastic syndrome (MDS) or untreated myelofibrosis (MF; N=57, 52%); and group 4: AML evolving from MDS or relapsed/refractory MDS or MF (N=20, 18%). Treatment consisted of decitabine 20 mg/m(2) daily for 5 days and GO 3 mg/m(2) on day 5. Post-induction therapy included five cycles of decitabine+GO followed by decitabine alone. Complete remission (CR)/CR with incomplete count recovery was achieved in 39 (35%) patients; group 1= 5/28 (17%), group 2=3/5 (60%), group 3=24/57 (42%) and group 4=7/20 (35%). The 8-week mortality in groups 3 and 4 was 16% and 10%, respectively. Common drug-related adverse events included nausea, mucositis and hemorrhage. Decitabine and GO improved the response rate but not overall survival compared with historical outcomes in untreated AML ⩾60 years.
Databáze: MEDLINE
Externí odkaz: