F. Ferrara et al., Fludarabine, cytarabine, and granulocyte-colony stimulating factor for thetreatment of high risk myelodysplastic syndromes, CANCER, 86(10), 1999, pp. 2006-2013
BACKGROUND. The prognosis of patients with high risk myelodysplastic syndro
mes (MDS) (i.e., refractory anemia with excess of blasts [RAEB] and refract
ory anemia with excess of blasts in transformation [RAEB-t]) usually is poo
r. The combination of fludarabine, cytarabine, and granulocyte-colony stimu
lating factor (G-CSF) (FLAG regimen) has been reported to be effective in p
atients with these diseases.
METHODS, Forty-two patients (32 with RAEB-t and 10 with RAEB) were treated
with the FLAG regimen. The median age was 61 years (range, 27-74 years). Fo
rty patients were diagnosed with primary MDS and 2 patients had treatment-r
elated MDS. Induction therapy was comprised of the FLAG regimen, whereas co
nsolidation therapy included idarubicin and cytarabine. Patients with a com
patible donor and who were age < 50 years were scheduled to undergo an allo
geneic bone marrow transplantation (BMT), whereas for those patients withou
t a donor and who were age < 60 years autologous BMT with peripheral blood
stem cells mobilized by the consolidation regimen plus G-CSF was planned.
RESULTS. Complete remission (CR) was achieved in 31 of 42 patients (74%; 95
% confidence interval, 60-87%). Death during induction therapy occurred in
4 patients (9%) whereas 7 patients (17%) were resistant to the FLAG regimen
. Toxicity from the consolidation regimen was negligible. All patients age
< 50 years and achieving CR were eligible for allogeneic BMT procedures, wi
th early recurrence being the only reason for exclusion. The median overall
survival and disease free survival were 13 months and 18 months, respectiv
ely. Patients with favorable cytogenetics had a significantly better outcom
e compared with those patients with an adverse karyotype.
CONCLUSIONS, The FLAG regimen is effective in patients with high risk MDS a
s well as in patients age > 60 years. The toxicity of the regimen is low an
d the majority of patients are eligible to undergo allogeneic BMT procedure
s after induction/consolidation therapy. [See editorial on pages 1893-9, th
is issue.] Cancer 1999;86:2006-13. (C) 1999 American Cancer Society.