Effects of azacitidine compared with conventional care regimens in elderly (≥75 years) patients with higher-risk myelodysplastic syndromes

被引:100
作者
Seymour, John F. [1 ,2 ]
Fenaux, Pierre [3 ,4 ]
Silverman, Lewis R. [5 ]
Mufti, Ghulam J. [6 ]
Hellstrom-Lindberg, Eva [7 ]
Santini, Valeria [8 ]
List, Alan F. [9 ]
Gore, Steven D. [10 ]
Backstrom, Jay [11 ]
McKenzie, David [11 ]
Beach, C. L. [11 ]
机构
[1] Peter MacCallum Canc Ctr, Melbourne, Vic 3002, Australia
[2] Univ Melbourne, Melbourne, Vic 3002, Australia
[3] Hop Avicenne, AP HP, Paris, France
[4] Univ Paris 13, F-93430 Villetaneuse, France
[5] Mt Sinai Sch Med, New York, NY USA
[6] Kings Coll London, Dept Haematol Med, London WC2R 2LS, England
[7] Karolinska Univ Hosp, Stockholm, Sweden
[8] Azienda Osped Careggi, Florence, Italy
[9] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[10] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD USA
[11] Celgene Corp, Summit, NJ USA
关键词
Azacitidine; Low-dose ara-C; Elderly; Myelodysplastic syndromes; MDS; Acute myeloid leukemia; AML; Survival; ACUTE MYELOID-LEUKEMIA; DOSE CYTOSINE-ARABINOSIDE; QUALITY-OF-LIFE; SCORING SYSTEM; CHEMOTHERAPY; CYTARABINE; CANCER; OLDER;
D O I
10.1016/j.critrevonc.2010.04.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This analysis compared azacitidine (AZA) to conventional care regimens (CCR) and their associated overall survival (OS) and tolerability in the subset of 87 elderly (>= 75 years) patients with higher-risk MDS (FAB: RAEB, RAEB-t, CMML and IPSS: Int-2 or High) from the AZA-001 trial. Patients were randomized to AZA (75 mg/m(2)/day subcutaneously x 7 days every 28 days) (n = 38) or CCR (n = 49) and had median ages of 78 and 77 years, respectively. AZA significantly improved OS vs CCR (HR: 0.48 [95%CI: 0.26, 0.89]; p = 0.0193) and 2-year OS rates were 55% vs 15% (p<0.001), respectively. AZA was generally well tolerated compared with CCR, which was primarily best supportive care (67%). Grade 3-4 anemia, neutropenia, and thrombocytopenia with AZA vs CCR were 13% vs 4%, 61% vs 17%, and 50% vs 30%, respectively. Given this efficacy and tolerability, AZA should be considered the treatment of choice in patients aged >= 75 years with good performance status and higher-risk MDS. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:218 / 227
页数:10
相关论文
共 26 条
  • [1] Alessandrino EP, 2002, HAEMATOLOGICA, V87, P1286
  • [2] Alymara V, 2004, J EXP CLIN CANC RES, V23, P447
  • [3] AUL C, 1989, CANCER-AM CANCER SOC, V64, P1812, DOI 10.1002/1097-0142(19891101)64:9<1812::AID-CNCR2820640909>3.0.CO
  • [4] 2-I
  • [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] A CRITICAL-APPRAISAL OF LOW-DOSE CYTOSINE-ARABINOSIDE IN PATIENTS WITH ACUTE NONLYMPHOCYTIC LEUKEMIA AND MYELODYSPLASTIC SYNDROMES
    CHESON, BD
    JASPERSE, DM
    SIMON, R
    FRIEDMAN, MA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1986, 4 (12) : 1857 - 1864
  • [7] Cheson BD, 2000, BLOOD, V96, P3671
  • [8] Deschler B, 2006, HAEMATOLOGICA, V91, P1513
  • [9] 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
    Fenaux, Pierre
    Mufti, Ghulam J.
    Hellstrom-Lindberg, Eva
    Santini, Valeria
    Finelli, Carlo
    Giagounidis, Aristoteles
    Schoch, Robert
    Gattermann, Norbert
    Sanz, Guillermo
    List, Alan
    Gore, Steven D.
    Seymour, John F.
    Bennett, John M.
    Byrd, John
    Backstrom, Jay
    Zimmerman, Linda
    McKenzie, David
    Beach, C. L.
    Silverman, Lewis R.
    [J]. LANCET ONCOLOGY, 2009, 10 (03) : 223 - 232
  • [10] International scoring system for evaluating prognosis in myelodysplastic syndromes
    Greenberg, P
    Cox, C
    LeBeau, MM
    Fenaux, P
    Morel, P
    Sanz, G
    Sanz, M
    Vallespi, T
    Hamblin, T
    Oscier, D
    Ohyashiki, K
    Toyama, K
    Aul, C
    Mufti, G
    Bennett, J
    [J]. BLOOD, 1997, 89 (06) : 2079 - 2088