| Literature DB >> 7682447 |
A Ganser1, G Heil, K Kolbe, G Maschmeyer, J T Fischer, L Bergmann, P S Mitrou, W Heit, H Heimpel, C Huber.
Abstract
Aggressive chemotherapy of advanced myelodysplastic syndrome (MDS), acute myeloid leukemia (AML) evolving from MDS, subacute AML and secondary AML has usually been associated with low complete remission (CR) rates, a high incidence of early death, and low disease-free survival. We therefore have initiated a phase-III trial of aggressive chemotherapy consisting of idarubicin, cytosine arabinoside, and VP-16 to improve the CR rate. Each chemotherapy cycle is followed by G-CSF to accelerate neutrophil recovery and to reduce the incidence of infections. Until now, 19 patients with high-risk AML have been entered. The CR rate is 47%, with only one death during induction. Patients achieving CR are randomized to receive either high-dose or low-dose interleukin-2 to eliminate residual leukemic cells and to prolong the duration of remission.Entities:
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Year: 1993 PMID: 7682447 DOI: 10.1007/bf01697620
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673