Treatment of high risk myelodysplastic syndromes with idarubicin and cytosine arabinoside supported by granulocyte-macrophage colony-stimulating factor (GM-CSF)

被引:24
作者
Economopoulos, T [1 ]
Papageorgiou, E [1 ]
Stathakis, N [1 ]
Constantinidou, M [1 ]
Parharidou, A [1 ]
Kostourou, A [1 ]
Dervenoulas, J [1 ]
Raptis, S [1 ]
机构
[1] LARISSA UNIV,SCH MED,DEPT INTERNAL MED,LARISA,GREECE
关键词
chemotherapy; GM-CSF; high risk myelodysplastic syndromes; treatment;
D O I
10.1016/0145-2126(95)00169-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this prospective study, patients with 'high risk' primary MDS, namely RAEB or RAEBt, were treated with combination chemotherapy (CT) supported by GM-CSF. The induction CT consisted of idarubicin 6 mg/m(2) days 1-3 and cytosine-arabinoside 200 mg/m(2) in 12 h infusion, days 1-5. The GM-CSF 3 mu g/kg s.c. was given on day 6 until the neutrophil count was 1x10(9)/I, Postremission CT consisted of two similar courses. Patients not in remission after two courses of CT were considered as treatment failures. Twenty-two patients with a median age of 64 years, range 50-79 years (11 RAEB and 11 RAEBt) were evaluable. Twelve out of 22 patients (54.5%) achieved complete remission (CR) and four, partial remission. Six patients were resistant to treatment; there were two toxic deaths; seven patients achieved CR after the first course and five after two courses. The median time of neutrophil recovery to 1x10(9)/I was day 15 (range 3-22) after the first course of treatment and day 14 (range 4-21) after the second. Thirteen out of 22 patients developed febrile episodes after the first course of treatment and nine after the second. The median duration of CR was 12 months. The median survival for CR patients was 24 months, for non-CR patients, 12 months; while survival for the whole population was 18 months. In conclusion, the results of this study indicate that the administration of moderately intensive CT supported by GM-CSF in 'poor risk' MDS gives promising results; the response rate is high for this disease, while the incidence of toxic death is low. GM-CSF appears to accelerate neutrophil recovery and probably reduces the incidence of infection. Copyright (C) 1996 Elsevier Science Ltd.
引用
收藏
页码:385 / 390
页数:6
相关论文
共 39 条
[31]   THE EVALUATION OF LOW-DOSE CYTARABINE IN THE TREATMENT OF MYELODYSPLASTIC SYNDROMES - A PHASE-III INTERGROUP STUDY [J].
MILLER, KB ;
KYUNGMANN, K ;
MORRISON, FS ;
WINTER, JN ;
BENNETT, JM ;
NEIMAN, RS ;
HEAD, DR ;
CASSILETH, PA ;
OCONNELL, MJ .
ANNALS OF HEMATOLOGY, 1992, 65 (04) :162-168
[32]  
MOREL P, 1993, LEUKEMIA, V7, P1315
[33]   MYELODYSPLASTIC SYNDROMES - A SCORING SYSTEM WITH PROGNOSTIC-SIGNIFICANCE [J].
MUFTI, GJ ;
STEVENS, JR ;
OSCIER, DG ;
HAMBLIN, TJ ;
MACHIN, D .
BRITISH JOURNAL OF HAEMATOLOGY, 1985, 59 (03) :425-433
[34]  
NAJEAN Y, 1977, BRIT J HAEMATOL, V37, P25, DOI 10.1111/j.1365-2141.1977.tb08760.x
[35]   HIGH-DOSE CYTOSINE-ARABINOSIDE IN THE TREATMENT OF PRELEUKEMIC DISORDERS - A LEUKEMIA INTERGROUP STUDY [J].
PREISLER, HD ;
RAZA, A ;
BARCOS, M ;
AZARNIA, N ;
LARSON, R ;
BROWMAN, G ;
WALKER, I ;
GRUNWALD, H ;
DARRIGO, P ;
STEIN, A ;
BLOOM, M ;
GOLDBERG, J ;
GOTTLIEB, A ;
BENNETT, J ;
KIRSHNER, J ;
PRIORE, R .
AMERICAN JOURNAL OF HEMATOLOGY, 1986, 23 (02) :131-134
[36]  
REIFFERS J, 1991, HAEMATOL BLOOD T, V34, P624
[37]  
STADTMAUER EA, 1991, BRIT J HAEMATOL, V77, P502
[38]   THE ROLE OF AGGRESSIVE CHEMOTHERAPY IN THE TREATMENT OF THE MYELODYSPLASTIC SYNDROMES [J].
TRICOT, G ;
BOOGAERTS, MA .
BRITISH JOURNAL OF HAEMATOLOGY, 1986, 63 (03) :477-483
[39]   A RANDOMIZED PHASE-I/II MULTICENTER STUDY OF RECOMBINANT HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR (GM-CSF) THERAPY FOR PATIENTS WITH MYELODYSPLASTIC SYNDROMES AND A RELATIVELY LOW-RISK OF ACUTE-LEUKEMIA [J].
WILLEMZE, R ;
VANDERLELY, N ;
ZWIERZINA, H ;
SUCIU, S ;
SOLBU, G ;
GERHARTZ, H ;
LABAR, B ;
VISANI, G ;
PEETERMANS, ME ;
JACOBS, A ;
STRYCKMANS, P ;
FENAUX, P ;
HAAK, HL ;
RIBEIRO, MM ;
BAUMELOU, E ;
BACCARANI, M ;
MANDELLI, F ;
JAKSIC, B ;
LOUWAGIE, A ;
THYSS, A ;
HAYAT, M ;
DECATALDO, F ;
STERN, AC ;
ZITTOUN, R .
ANNALS OF HEMATOLOGY, 1992, 64 (04) :173-180