Ganser A, Heil G, Kolbe K, Maschmeyer G, Fischer J T, Bergmann L, Mitrou P S, Heit W, Heimpel H, Huber C
Abteilung für Hämatologie, Klinikum der Universität Frankfurt, Germany.
Ann Hematol. 1993 Mar;66(3):123-5. doi: 10.1007/BF01697620.
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.