Intermediate Dose Cytarabine and Idarubicin for Salvage Therapy of Acute Myeloid Leukemia

作者: G. Schott , A. Grüneisen , H. H. Fülle , C. Sperling , M. Notter

DOI: 10.1007/978-3-642-71960-8_131

关键词:

摘要: Between September 1991 and May 1996, 56 patients with refractory or relapsed acute myeloid leukemia (AML) were treated one cycle of timed sequential chemotherapy (TSC) consisting intermediate-dose (ID) ara-C (1.0 g/m2 every 12 h) on days 1, 2, 8, 9, idarubicin (IDA, 10 mg/m2) 3, 4, 10, 11. The study population included 22 AML, 33 late first relapse occurring after a complete remission ≥ 6 months, 1 patient for whom the clinical course before salvage therapy was unknown. Of entered onto study, 25 (45%) achieved (CR), 8 (14%) partial (PR), 11 (20%) classified as treatment failure due to resistant disease, (21%) died within 42 initiation therapy, mainly infections. Response strongly influenced by disease status 55% achieving CR compared 32% refractoryAML. Severe myelosuppression observed in most resulting fever documented infections 70–90% them whereas nonhematologic toxicity tolerable. Among who CR, received no postremission 2 cycles IDA (8 etoposide (150 3 consolidation, underwent an allogeneic autologous bone marrow transplantation (BMT), lost follow-up. Overall, median follow-up 44 duration is 9 survival months well. We conclude that this regimen has significant antileukemic efficacy, especially AML durable (≥ months). short not eligible BMT, however, emphasizes need optimizing early postinduction therapy.

参考文章(25)
E Archimbaud, V Leblond, M Michallet, C Cordonnier, P Fenaux, P Travade, F Dreyfus, J Jaubert, Y Devaux, D Fiere, Intensive sequential chemotherapy with mitoxantrone and continuous infusion etoposide and cytarabine for previously treated acute myelogenous leukemia Blood. ,vol. 77, pp. 1894- 1900 ,(1991) , 10.1182/BLOOD.V77.9.1894.1894
E Estey, Treatment of refractory AML. Leukemia. ,vol. 10, pp. 932- 936 ,(1996)
T. Büchner, , W. Hiddemann, B. Wörmann, G. Maschmeyer, W. Heit, C. Aul, A. Heyll, H. Löffler, H. Gassmann, H. H. Fülle, K. P. Hellriegel, W.-D. Ludwig, E. Lengfelder, B. Lathan, B. Emmerich, U. W. Schaefer, M. C. Sauerland, A. Heinecke, Chemotherapy Intensity and Long-Term Outcome in AML Haematology and Blood Transfusion / Hämatologie und Bluttransfusion. pp. 513- 518 ,(1994) , 10.1007/978-3-642-78350-0_92
T. Buechner, W. Hiddemann, Treatment strategies in acute myeloid leukemia (AML) Annals of Hematology. ,vol. 60, pp. 61- 67 ,(1990) , 10.1007/BF01728798
W Hiddemann, H Kreutzmann, K Straif, WD Ludwig, R Mertelsmann, R Donhuijsen- Ant, E Lengfelder, Z Arlin, T Buchner, High-dose cytosine arabinoside and mitoxantrone: a highly effective regimen in refractory acute myeloid leukemia. Blood. ,vol. 69, pp. 744- 749 ,(1987) , 10.1182/BLOOD.V69.3.744.744
M J Keating, H Kantarjian, T L Smith, E Estey, R Walters, B Andersson, M Beran, K B McCredie, E J Freireich, Response to salvage therapy and survival after relapse in acute myelogenous leukemia. Journal of Clinical Oncology. ,vol. 7, pp. 1071- 1080 ,(1989) , 10.1200/JCO.1989.7.8.1071
S Amadori, W Arcese, G Isacchi, G Meloni, M C Petti, B Monarca, A M Testi, F Mandelli, Mitoxantrone, etoposide, and intermediate-dose cytarabine: an effective and tolerable regimen for the treatment of refractory acute myeloid leukemia. Journal of Clinical Oncology. ,vol. 9, pp. 1210- 1214 ,(1991) , 10.1200/JCO.1991.9.7.1210
V Gandhi, E Estey, M J Keating, W Plunkett, Fludarabine potentiates metabolism of cytarabine in patients with acute myelogenous leukemia during therapy. Journal of Clinical Oncology. ,vol. 11, pp. 116- 124 ,(1993) , 10.1200/JCO.1993.11.1.116
H M Kantarjian, M J Keating, R S Walters, K B McCredie, E J Freireich, The characteristics and outcome of patients with late relapse acute myelogenous leukemia. Journal of Clinical Oncology. ,vol. 6, pp. 232- 238 ,(1988) , 10.1200/JCO.1988.6.2.232