TY - JOUR
T1 - Azacitidine in the treatment of therapy related myelodysplastic syndrome and acute myeloid leukemia (tMDS/AML)
T2 - A report on 54 patients by the Groupe Francophone Des Myelodysplasies (GFM)
AU - Bally, Cecile
AU - Thépot, Sylvain
AU - Quesnel, Bruno
AU - Vey, Norbert
AU - Dreyfus, Francois
AU - Fadlallah, Jehane
AU - Turlure, Pascal
AU - de Botton, Stephane
AU - Dartigeas, Caroline
AU - de Renzis, Benoit
AU - Itzykson, Raphael
AU - Fenaux, Pierre
AU - Adès, Lionel
PY - 2013/6/1
Y1 - 2013/6/1
N2 - The effect of azacitidine (AZA) in therapy related MDS and AML (t-MDS/AML) is not well established. 54 patients (42 t-MDS and 12 t-AML), 71% of whom had complex karyotype, received AZA for at least one cycle (median 4 cycles). The overall response rate (ORR) was 39% in the whole cohort and 62% in patients who received ≥4 cycles. One, 2 and 3 year OS was 36%, 14% and 8% respectively. Female gender (p=0.01) and ECOG 0-1 (p= 0.04) were associated with significantly better OS, while karyotype and marrow blast percentage had no significant impact. By comparison with de novo MDS/AML treated in the same program, t-MDS/AML had a similar response rate (38% vs 45% in de novo MDS/AML, p= 0.53), but significantly shorter OS (2 year OS of 14% vs 33.9%, p=0.0005). However, in a multivariate analysis performed in all patients (de novo and therapy related cases), only complex karyotype and high IPSS, and not etiology (i.e. de novo versus therapy related), had a significant impact on OS. Nine (15%) patients received allogeneic stem cell transplantation, 4 of whom were still alive.
AB - The effect of azacitidine (AZA) in therapy related MDS and AML (t-MDS/AML) is not well established. 54 patients (42 t-MDS and 12 t-AML), 71% of whom had complex karyotype, received AZA for at least one cycle (median 4 cycles). The overall response rate (ORR) was 39% in the whole cohort and 62% in patients who received ≥4 cycles. One, 2 and 3 year OS was 36%, 14% and 8% respectively. Female gender (p=0.01) and ECOG 0-1 (p= 0.04) were associated with significantly better OS, while karyotype and marrow blast percentage had no significant impact. By comparison with de novo MDS/AML treated in the same program, t-MDS/AML had a similar response rate (38% vs 45% in de novo MDS/AML, p= 0.53), but significantly shorter OS (2 year OS of 14% vs 33.9%, p=0.0005). However, in a multivariate analysis performed in all patients (de novo and therapy related cases), only complex karyotype and high IPSS, and not etiology (i.e. de novo versus therapy related), had a significant impact on OS. Nine (15%) patients received allogeneic stem cell transplantation, 4 of whom were still alive.
KW - Azacitidine
KW - Myelodysplastic syndromes
KW - Therapy-related MDS/AML
UR - http://www.scopus.com/inward/record.url?scp=84877062091&partnerID=8YFLogxK
U2 - 10.1016/j.leukres.2013.02.014
DO - 10.1016/j.leukres.2013.02.014
M3 - Article
C2 - 23499498
AN - SCOPUS:84877062091
SN - 0145-2126
VL - 37
SP - 637
EP - 640
JO - Leukemia Research
JF - Leukemia Research
IS - 6
ER -