Addition of Gemtuzumab Ozogamicin to Induction Chemotherapy Improves Survival in Older Patients With Acute Myeloid Leukemia

被引:328
作者
Burnett, Alan K. [1 ]
Russell, Nigel H. [3 ]
Hills, Robert K.
Kell, Jonathan [2 ]
Freeman, Sylvie [4 ]
Kjeldsen, Lars [10 ]
Hunter, Ann E. [7 ]
Yin, John [8 ]
Craddock, Charles F. [5 ]
Dufva, Inge Hoegh [9 ]
Wheatley, Keith [4 ]
Milligan, Donald [6 ]
机构
[1] Cardiff Univ, Sch Med, Dept Haematol, Cardiff CF14 4XN, S Glam, Wales
[2] Univ Wales Hosp, Cardiff CF4 4XW, S Glam, Wales
[3] Univ Nottingham Hosp, Natl Hlth Serv Trust, Nottingham NG7 2UH, England
[4] Univ Birmingham, Birmingham B15 2TT, W Midlands, England
[5] Queen Elizabeth Hosp, Birmingham, England
[6] Birmingham Heartlands Hosp, Birmingham, England
[7] Leicester Royal Infirm, Leicester, Leics, England
[8] Manchester Royal Infirm, Manchester M13 9WL, Lancs, England
[9] Herlev Hosp, Copenhagen, Denmark
[10] Rigshosp, Copenhagen, Denmark
关键词
ANTI-CD33; MONOCLONAL-ANTIBODY; THERAPY; TRIAL; EFFICACY; DISEASE; SAFETY; CELLS; AML;
D O I
10.1200/JCO.2012.42.2964
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose There has been little survival improvement in older patients with acute myeloid leukemia (AML) in the last two decades. Improving induction treatment may improve the rate and quality of remission and consequently survival. In our previous trial, in younger patients, we showed improved survival for the majority of patients when adding gemtuzumab ozogamicin (GO) to induction chemotherapy. Patients and Methods Untreated patients with AML or high-risk myelodysplastic syndrome (median age, 67 years; range, 51 to 84 years) were randomly assigned to receive induction chemotherapy with either daunorubicin/ara-C or daunorubicin/clofarabine, with (n = 559) or without (n = 556) GO 3 mg/m(2) on day 1 of course one of therapy. The primary end point was overall survival (OS). Results The overall response rate was 69% (complete remission [CR], 60%; CR with incomplete recovery [CRi], 9%), with no difference between GO (70%) and no GO (68%) arms. There was no difference in 30- or 60-day mortality and no major increase in toxicity with GO. With median follow-up of 30 months (range, 5.5 to 54.6 months), 3-year cumulative incidence of relapse was significantly lower with GO (68% v 76%; hazard ratio [HR], 0.78; 95% CI, 0.66 to 0.93; P = .007), and 3-year survival was significantly better (25% v 20%; HR, 0.87; 95% CI, 0.76 to 1.00; P = .05). The benefit was apparent across subgroups. There was no interaction with other treatment interventions. A meta-analysis of 2,228 patients in two United Kingdom National Cancer Research Institute trials showed significant improvements in relapse (HR, 0.82; 95% CI, 0.72 to 0.93; P = .002) and OS (HR, 0.88; 95% CI, 0.79 to 0.98; P = .02). Conclusion Adding GO (3 mg/m(2)) to induction chemotherapy reduces relapse risk and improves survival with little increase in toxicity. J Clin Oncol 30:3924-3931. (C) 2012 by American Society of Clinical Oncology
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页码:3924 / 3931
页数:8
相关论文
共 23 条
[1]  
[Anonymous], 1990, TREATM EARL BREAST C
[2]   Age and acute myeloid leukemia [J].
Appelbaum, FR ;
Gundacker, H ;
Head, DR ;
Slovak, ML ;
Willman, CL ;
Godwin, JE ;
Anderson, JE ;
Petersdorf, SH .
BLOOD, 2006, 107 (09) :3481-3485
[3]  
BURNETT AK, 2006, BLOOD, V108, pA551
[4]   Therapeutic Advances in Acute Myeloid Leukemia [J].
Burnett, Alan ;
Wetzler, Meir ;
Loewenberg, Bob .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (05) :487-494
[5]   Identification of Patients With Acute Myeloblastic Leukemia Who Benefit From the Addition of Gemtuzumab Ozogamicin: Results of the MRC AML15 Trial [J].
Burnett, Alan K. ;
Hills, Robert K. ;
Milligan, Donald ;
Kjeldsen, Lars ;
Kell, Jonathan ;
Russell, Nigel H. ;
Yin, John A. L. ;
Hunter, Ann ;
Goldstone, Anthony H. ;
Wheatley, Keith .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (04) :369-377
[6]  
CARON PC, 1994, BLOOD, V83, P1760
[7]  
Caron PC, 1998, CLIN CANCER RES, V4, P1421
[8]   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 [J].
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 .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (24) :4642-4649
[9]   Phase III randomized multicenter study of a humanized anti-CD33 monoclonal antibody, lintuzumab, in combination with chemotherapy, versus chemotherapy alone in patients with refractory or first-relapsed acute myeloid leukemia [J].
Feldman, EJ ;
Brandwein, J ;
Stone, R ;
Kalaycio, M ;
Moore, J ;
O'Connor, J ;
Wedel, N ;
Roboz, GJ ;
Miller, C ;
Chopra, R ;
Jurcic, JC ;
Brown, R ;
Ehmann, WC ;
Schulman, P ;
Frankel, SR ;
De Angelo, D ;
Scheinberg, D .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (18) :4110-4116
[10]   Anthracycline Dose Intensification in Acute Myeloid Leukemia [J].
Fernandez, Hugo F. ;
Sun, Zhuoxin ;
Yao, Xiaopan ;
Litzow, Mark R. ;
Luger, Selina M. ;
Paietta, Elisabeth M. ;
Racevskis, Janis ;
Dewald, Gordon W. ;
Ketterling, Rhett P. ;
Bennett, John M. ;
Rowe, Jacob M. ;
Lazarus, Hillard M. ;
Tallman, Martin S. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (13) :1249-1259