TY - JOUR
T1 - Outcome of therapy-related myeloid neoplasms treated with azacitidine
AU - Fianchi, Luana
AU - Criscuolo, Marianna
AU - Lunghi, Monia
AU - Gaidano, Gianluca
AU - Breccia, Massimo
AU - Levis, Alessandro
AU - Finelli, Carlo
AU - Santini, Valeria
AU - Musto, Pellegrino
AU - Oliva, Esther N.
AU - Leoni, Pietro
AU - Spiriti, Antonietta Aloe
AU - Dal, Francesco
AU - Hohaus, Stefan
AU - Pagano, Livio
AU - Leone, Giuseppe
AU - Voso, Maria Teresa
N1 - Funding Information:
This work was supported by grants from Associazione Italiana Ricerca sul Cancro (A.I.R.C.) and FIRB (RBAP11TF7Z).
PY - 2012
Y1 - 2012
N2 - Background: Therapy-related myeloid neoplasms (t-MN), including myelodysplastic syndromes and acute myeloid leukemia (t-MDS and t-AML) are associated to clinical and biologic unfavorable prognostic features, including high levels of DNA methylation. Methods. We retrospectively evaluated 50t-MN patients (34 MDS and 16 AML) selected among all patients receiving azacitidine (AZA) at 10 Italian Hematology Centers. Patients had developed a t-MN at a median of 6.5years (range 1.7- 29) after treatment of the primary tumor (hematological neoplasm, 27 patients; solid tumor, 23 patients). Results: The overall response rate was 42% (complete remission: 10 patients, partial remission: 2 and hematological improvement: 8 patients) and was obtained after a median of 3 cycles (range 1-6). Median overall survival (OS) was 21months (range 1-53.6+) from AZA start. OS was significantly better in patients with less than 20% blasts, in normal karyotype t-AML and when AZA was used as front-line treatment. This was confirmed by the multivariate analysis. Conclusions: This study reports efficacy of AZA in the largest series of therapy-related MN patients treated with 5-AZA. Our data show that blasts and karyotype maintain their important prognostic role in t-MN also in the azacitidine era.
AB - Background: Therapy-related myeloid neoplasms (t-MN), including myelodysplastic syndromes and acute myeloid leukemia (t-MDS and t-AML) are associated to clinical and biologic unfavorable prognostic features, including high levels of DNA methylation. Methods. We retrospectively evaluated 50t-MN patients (34 MDS and 16 AML) selected among all patients receiving azacitidine (AZA) at 10 Italian Hematology Centers. Patients had developed a t-MN at a median of 6.5years (range 1.7- 29) after treatment of the primary tumor (hematological neoplasm, 27 patients; solid tumor, 23 patients). Results: The overall response rate was 42% (complete remission: 10 patients, partial remission: 2 and hematological improvement: 8 patients) and was obtained after a median of 3 cycles (range 1-6). Median overall survival (OS) was 21months (range 1-53.6+) from AZA start. OS was significantly better in patients with less than 20% blasts, in normal karyotype t-AML and when AZA was used as front-line treatment. This was confirmed by the multivariate analysis. Conclusions: This study reports efficacy of AZA in the largest series of therapy-related MN patients treated with 5-AZA. Our data show that blasts and karyotype maintain their important prognostic role in t-MN also in the azacitidine era.
KW - Hypomethylating agents
KW - Therapy related myeloid neoplasms
UR - http://www.scopus.com/inward/record.url?scp=84864400766&partnerID=8YFLogxK
U2 - 10.1186/1756-8722-5-44
DO - 10.1186/1756-8722-5-44
M3 - Article
SN - 1756-8722
VL - 5
JO - Journal of Hematology and Oncology
JF - Journal of Hematology and Oncology
M1 - 44
ER -