EFFICACY OF ERYTHROPOIETIN IN THE MYELODYSPLASTIC SYNDROMES - A METAANALYSIS OF 205 PATIENTS FROM 17 STUDIES

被引:265
作者
HELLSTROMLINDBERG, E
机构
[1] Department of Medicine. Division of Haematology, Huddinge University Hospital, Stockholm
关键词
ERYTHROPOIETIN; MYELODYSPLASTIC SYNDROMES; PREDICTIVE FACTORS;
D O I
10.1111/j.1365-2141.1995.tb08909.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Erythropoietin (epo) can be used to improve the anaemia of patients with myelodysplastic syndromes (MDS), but the efficacy is relatively low and the treatment is expensive. So far, no individual clinical trial has been sufficiently extensive to provide a basis for a decision model for the use of epo in MDS. This meta-analysis included 17 original articles with a total of 205 patients with MDS who had been treated with epo. 33 patients (16%) showed a significant response to treatment. Patients with refractory anaemia with ring sideroblasts (RAS) showed a lower response rate than all other patients (7.5% v 21%, P=0.010). The difference in response rate between patients with and without transfusion need was also highly significant (10% v 44%, P < 0.001). The serum level of epo was significantly lower in the responding patients, but this parameter on its own could not be used to identify patients with a favourable response. FAB group (RAS versus others), transfusion need and s-epo (>/<200 U/l) were combined in a model to provide information about the probability of response in different groups of patients. Patients with no transfusion requirement and MDS other than RAS showed a response rate of greater than or equal to 50%, irrespective of their serum level of epo. In patients with RAS and s-epo >200 U/l, no response was observed. In the remaining groups the response rates varied between 9% and 33%. This meta-analysis shows that the efficacy of epo in MDS in general was low, but that groups of patients with an acceptable response rate could be identified.
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页码:67 / 71
页数:5
相关论文
共 29 条
  • [1] ADAMSON JW, 1992, ACTA HAEMATOL-BASEL, V87, P20
  • [2] PROPOSALS FOR THE CLASSIFICATION OF THE MYELODYSPLASTIC SYNDROMES
    BENNETT, JM
    CATOVSKY, D
    DANIEL, MT
    FLANDRIN, G
    GALTON, DAG
    GRALNICK, HR
    SULTAN, C
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1982, 51 (02) : 189 - 199
  • [3] IMPROVEMENT OF ANEMIA BY RECOMBINANT ERYTHROPOIETIN IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES AND APLASTIC-ANEMIA
    BESSHO, M
    JINNAI, I
    MATSUDA, A
    SAITO, M
    HIRASHIMA, K
    [J]. INTERNATIONAL JOURNAL OF CELL CLONING, 1990, 8 (06): : 445 - 458
  • [4] THE TREATMENT OF ANEMIA IN THE MYELODYSPLASTIC SYNDROMES WITH RECOMBINANT-HUMAN-ERYTHROPOIETIN
    BOWEN, D
    CULLIGAN, D
    JACOBS, A
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1991, 77 (03) : 419 - 423
  • [5] CAZZOLA M, 1992, BLOOD, V79, P29
  • [6] APOPTOSIS IS A COMMON HISTOPATHOLOGICAL FINDING IN MYELODYSPLASIA - THE CORRELATE OF INEFFECTIVE HEMATOPOIESIS
    CLARK, DM
    LAMPERT, IA
    [J]. LEUKEMIA & LYMPHOMA, 1990, 2 (06) : 415 - 418
  • [7] HIGH-DOSES OF INTRAVENOUS RECOMBINANT ERYTHROPOIETIN FOR THE TREATMENT OF ANEMIA IN MYELODYSPLASTIC SYNDROME
    GOY, A
    BELANGER, C
    CASADEVALL, N
    PICARD, F
    GUESNU, M
    JAULMES, D
    POISSON, D
    VARET, B
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1993, 84 (02) : 232 - 237
  • [8] RECOMBINANT HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR PLUS RECOMBINANT-HUMAN-ERYTHROPOIETIN MAY IMPROVE ANEMIA IN SELECTED PATIENTS WITH MYELODYSPLASTIC SYNDROMES
    HANSEN, PB
    JOHNSEN, HE
    HIPPE, E
    HELLSTROMLINDBERG, E
    RALFKIAER, E
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 1993, 44 (04) : 229 - 236
  • [9] HELLSTROM E, 1991, EUR J HAEMATOL, V47, P355
  • [10] HELLSTROMLINDBE.E, 1992, LEUKEMIA RES, V16, P529