Efficacy of azacitidine compared with that of conventional care regimens in the treatment of higher-risk myelodysplastic syndromes: a randomised, open-label, phase III study

被引:2079
作者
Fenaux, Pierre [1 ]
Mufti, Ghulam J. [2 ]
Hellstrom-Lindberg, Eva [3 ]
Santini, Valeria [4 ]
Finelli, Carlo [5 ]
Giagounidis, Aristoteles [6 ]
Schoch, Robert [7 ]
Gattermann, Norbert [8 ]
Sanz, Guillermo [9 ]
List, Alan [10 ]
Gore, Steven D. [11 ]
Seymour, John F. [12 ,17 ]
Bennett, John M. [13 ]
Byrd, John [14 ]
Backstrom, Jay [15 ]
Zimmerman, Linda [15 ]
McKenzie, David [15 ]
Beach, C. L. [15 ]
Silverman, Lewis R. [16 ]
机构
[1] Univ Paris 13, Hop Avicenne, Serv Hematol Clin, F-93009 Bobigny, France
[2] Kings Coll Hosp London, London, England
[3] Karolinska Univ Hosp, Stockholm, Sweden
[4] Univ Careggi, Azienda Osped, Florence, Italy
[5] Inst Hematol Seragnoli, Bologna, Italy
[6] St Johannes Hosp, Duisburg, Germany
[7] Univ Klinikum Schleswig Holstein, Kiel, Germany
[8] Univ Klinikum Dusseldorf, Dusseldorf, Germany
[9] Hosp Univ La Fe, Valencia, Spain
[10] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[11] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD USA
[12] Peter MacCallum Canc Ctr, Melbourne, Australia
[13] Univ Rochester, Med Ctr, James P Wilmot Canc Ctr, Rochester, NY 14642 USA
[14] Ohio State Univ, Sch Med & Publ Hlth, Columbus, OH 43210 USA
[15] Celgene Corp, Summit, NJ USA
[16] Mt Sinai Sch Med, New York, NY USA
[17] Univ Melbourne, Melbourne, Vic 3010, Australia
关键词
ACUTE MYELOID-LEUKEMIA; INTERNATIONAL WORKING GROUP; STEM-CELL TRANSPLANTATION; LOW-DOSE CYTARABINE; INTENSIVE CHEMOTHERAPY; ARA-C; DNA METHYLTRANSFERASE; RESPONSE CRITERIA; CLASSIFICATION; FLUDARABINE;
D O I
10.1016/S1470-2045(09)70003-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Drug treatments for patients with high-risk myelodysplastic syndromes provide no survival advantage. In this trial, we aimed to assess the effect of azacitidine on overall survival compared with the three commonest conventional care regimens. Methods In a phase III, international, multicentre, controlled, parallel-group, open-label trial, patients with higher-risk myelodysplastic syndromes were randomly assigned one-to-one to receive azacitidine (75 mg/m(2) per day for 7 days every 28 days) or conventional care (best supportive care, low-dose cytarabine, or intensive chemotherapy as selected by investigators before randomisation). Patients were stratified by French-American-British and international prognostic scoring system classifications; randomisation was done with a block size of four. The primary endpoint was overall survival. Efficacy analyses were by intention to treat for all patients assigned to receive treatment. This study is registered with ClinicalTrials.gov, number NCT00071799. Findings Between Feb 13, 2004, and Aug 7, 2006, 358 patients were randomly assigned to receive azacitidine (n=179) or conventional care regimens (n=179). Four patients in the azacitidine and 14 in the conventional care groups received no study drugs but were included in the intention-to-treat efficacy analysis. After a median follow-up of 21.1 months (IQR 15.1-26.9), median overall survival was 24.5 months (9-9-not reached) for the azacitidine group versus 15 0 months (5.6-24.1) for the conventional care group (hazard ratio 0.58; 95% CI 0.43-0.77; stratified log-rank p=0.0001). At last follow-up, 82 patients in the azacitidine group had died compared with 113 in the conventional care group. At 2 years, on the basis of Kaplan-Meier estimates, 50.8% (95% Cl 42.1-58.8) of patients in the azacitidine group were alive compared with 26.2% (18.7-34.3) in the conventional care group (p < 0.0001). Peripheral cytopenias were the most common grade 3-4 adverse events for all treatments. Interpretation Treatment with azacitidine increases overall survival in patients with higher-risk myelodysplastic syndromes relative to conventional care.
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页码:223 / 232
页数:10
相关论文
共 38 条
  • [1] Alessandrino EP, 2002, HAEMATOLOGICA, V87, P1286
  • [2] Allogeneic stem cell transplantation for myelodysplastic syndrome
    Barrett, A. John
    Savani, Bipin N.
    [J]. SEMINARS IN HEMATOLOGY, 2008, 45 (01) : 49 - 59
  • [3] 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
  • [4] Guidelines for the diagnosis and therapy of adult myelodysplastic syndromes
    Bowen, D
    Culligan, D
    Jowitt, S
    Kelsey, S
    Mufti, G
    Oscier, D
    Parker, J
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2003, 120 (02) : 187 - 200
  • [5] A comparison of low-dose cytarabine and hydroxyurea with or without all-trans retinoic acid for acute myeloid leukemia and high-risk myelodysplastic syndrome in patients not considered fit for intensive treatment
    Burnett, Alan K.
    Milligan, Donald
    Prentice, Archie G.
    Goldstone, Anthony H.
    McMullin, Mary F.
    Hills, Robert K.
    Wheatley, Keith
    [J]. CANCER, 2007, 109 (06) : 1114 - 1124
  • [6] Cheson BD, 2000, BLOOD, V96, P3671
  • [7] Revised recommendations of the international working group for diagnosis, standardization of response criteria, treatment outcomes, and reporting standards for therapeutic trials in acute myeloid leukemia
    Cheson, BD
    Bennett, JM
    Kopecky, KJ
    Büchner, T
    Willman, CL
    Estey, EH
    Schiffer, CA
    Döhner, H
    Tallman, MS
    Lister, TA
    LoCocco, F
    Willemze, R
    Biondi, A
    Hiddemann, W
    Larson, RA
    Löwenberg, B
    Sanz, MA
    Head, DR
    Ohno, R
    Bloomfield, CD
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (24) : 4642 - 4649
  • [8] CHESON BD, 1987, SEMIN ONCOL, V14, P126
  • [9] CHESON ED, 1998, LEUK RES S1, V22, pS17
  • [10] COX DR, 1972, J R STAT SOC B, V34, P187