High dose intermittent ARA-C (HiDAC) for consolidation of patients with de novo AML: a single center experience

Leuk Res. 2005 Jun;29(6):609-15. doi: 10.1016/j.leukres.2004.10.009. Epub 2005 Jan 25.

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.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Cytarabine / therapeutic use*
  • Daunorubicin / therapeutic use*
  • Dose-Response Relationship, Drug
  • Etoposide / therapeutic use*
  • Female
  • Humans
  • Leukemia, Myeloid, Acute / drug therapy*
  • Male
  • Middle Aged
  • Prognosis
  • Risk Factors
  • Survival Analysis
  • Treatment Outcome

Substances

  • Cytarabine
  • Etoposide
  • Daunorubicin

Supplementary concepts

  • DAV regimen