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    Leukemia research. 2005 Jan 25. pii: S0145-2126(04)00381-9. doi: 10.1016/j.leukres.2004.10.009
    High dose intermittent ARA-C (HiDAC) for consolidation of patients with de novo AML: a single center experience.
    Böhm A1,  Piribauer M,  Wimazal F,  Geissler K,  Gisslinger H,  Knöbl P,  Jäger U,  Fonatsch C,  Kyrle PA,  Valent P,  Lechner K,  Sperr WR
    Author information
    1Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
    Abstract

    High dose intermittent ARA-C (2x3 g/m(2) i.v., days 1, 3, 5)=HiDAC was introduced as consolidation in AML by the CALGB-group in 1994. We treated 44 de novo AML patients in CR with up to four cycles of HiDAC (four cycles: 56.8%; three cycles: 22.7%; two cycles: 6.8%; one cycle: 13.7%). Median duration of aplasia (ANC<0.5x10(9)/l) was 12 days. Neutropenic fever occurred in 38.6% of the patients during the first, 52.6% during the second, 45.7% during the third, and in 40% during the fourth cycle. Non-hematologic toxicity was tolerable. The median overall- and disease-free survival were 19.3 and 11.3 months, respectively. The best outcome was seen in patients aged <40 years. These results confirm that HiDAC is a safe and effective consolidation in AML.


    Publikations ID: 15863199
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