Open Access Research

Outcome of therapy-related myeloid neoplasms treated with azacitidine

Luana Fianchi1, Marianna Criscuolo1, Monia Lunghi2, Gianluca Gaidano2, Massimo Breccia3, Alessandro Levis4, Carlo Finelli5, Valeria Santini6, Pellegrino Musto7, Esther N Oliva8, Pietro Leoni9, Antonietta Aloe Spiriti10, Francesco D’Alò1, Stefan Hohaus1, Livio Pagano1, Giuseppe Leone1 and Maria T Voso1*

Author Affiliations

1 Istituto di Ematologia, Università Cattolica del Sacro Cuore, 00168, Roma, Italy

2 Ematologia, Dipartimento di Medicina Traslazionale, Università del Piemonte Orientale Amedeo Avogadro, Novara, Italy

3 Ematologia, Università La Sapienza, Roma, Italy

4 Ospedale di Alessandria, Alessandria, Italy

5 Universita' di Bologna, Bologna, Italy

6 Ematologia Firenze, Firenze, Italy

7 Dipartimento Onco-Ematologico, IRCCS, Centro di Riferimento Oncologico della Basilicata, Rionero in Vulture, Italy

8 Azienda Ospedaliera Bianchi-Melacrino-Morelli, Reggio Calabria, Italy

9 Ematologia Ancona, Ancona, Italy

10 Ospedale Sant’Andrea, Roma, Italy

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Journal of Hematology & Oncology 2012, 5:44 doi:10.1186/1756-8722-5-44

Published: 1 August 2012

Abstract

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 50 t-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 6.5 years (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 21 months (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.

Keywords:
Therapy related myeloid neoplasms; Hypomethylating agents