Autologous peripheral blood stem cell transplantation for acute myeloid leukemia

被引:105
|
作者
Vellenga, Edo [1 ,2 ]
van Putten, Wim [3 ,4 ]
Ossenkoppele, Gert J. [5 ]
Verdonck, Leo F. [6 ]
Theobald, Matthias [7 ]
Cornelissen, Jan J. [8 ]
Huijgens, Peter C. [5 ]
Maertens, Johan [9 ]
Gratwohl, Alois [10 ]
Schaafsma, Ron [11 ]
Schanz, Urs [12 ]
Graux, Carlos [13 ]
Schouten, Harry C. [14 ]
Ferrant, Augustin [15 ]
Bargetzi, Mario [16 ]
Fey, Martin F. [17 ,18 ]
Lowenberg, Bob [8 ]
机构
[1] Univ Med Ctr Groningen, Dept Hematol, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Dept Hematol, Groningen, Netherlands
[3] Erasmus Univ, Hovon Data Ctr, Med Ctr Rotterdam, Rotterdam, Netherlands
[4] Erasmus Univ, Dept Trials & Stat, Med Ctr Rotterdam, Rotterdam, Netherlands
[5] Vrije Univ Amsterdam, Dept Hematol, Med Ctr Amsterdam, Amsterdam, Netherlands
[6] Univ Med Ctr Utrecht, Utrecht, Netherlands
[7] Univ Hosp Mainz, Dept Internal Med 3, Mainz, Germany
[8] Erasmus Univ, Dept Hematol, Med Ctr Rotterdam, Rotterdam, Netherlands
[9] Univ Hosp Gasthuisberg, B-3000 Louvain, Belgium
[10] Univ Basel Hosp, CH-4031 Basel, Switzerland
[11] Med Spectrum Twente, Enschede, Netherlands
[12] Univ Zurich Hosp, Div Hematol, CH-8091 Zurich, Switzerland
[13] MT Godinne, UCL, Yvoir, Belgium
[14] Univ Med Ctr Maastricht, Maastricht, Netherlands
[15] Hosp St Luc, Brussels, Belgium
[16] Kantonsspittal Aarau, Ctr Hematol Oncol & Transfus Med, Aarau, Switzerland
[17] Univ Bern, Dept Med Oncol, Bern, Switzerland
[18] Inselspital Bern, CH-3010 Bern, Switzerland
关键词
BONE-MARROW-TRANSPLANTATION; ACUTE MYELOGENOUS LEUKEMIA; COLONY-STIMULATING FACTOR; 1ST COMPLETE REMISSION; HIGH-DOSE CYTARABINE; INTENSIVE CHEMOTHERAPY; POSTREMISSION THERAPY; DAUNORUBICIN; MUTATIONS; ADULTS;
D O I
10.1182/blood-2011-07-370247
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report the results of a prospective, randomized phase 3 trial evaluating autologous peripheral blood stem cell transplantation (ASCT) versus intensive consolidation chemotherapy in newly diagnosed AML patients in complete remission (CR1). Patients with AML (16-60 years) in CR1 after 2 cycles of intensive chemotherapy and not eligible for allogeneic SCT were randomized between intensive chemotherapy with etoposide and mitoxantrone or ASCT ater high-dose cyclophosphamide and busulfan. Of patients randomized (chemotherapy, n = 259; ASCT, n = 258), more than 90% received their assigned treatment. The 2 groups were comparable with regard to prognostic factors. The ASCT group showed a markedly reduced relapse rate (58% vs 70%, P = .02) and better relapse-free survival at 5 years (38% vs 29%, P = .065, hazard ratio = 0.82; 95% confidence interval, 0.66-1.1) with nonrelapse mortality of 4% versus 1% in the chemotherapy arm (P = .02). Overall survival was similar (44% vs 41% at 5 years, P = .86) because of more opportunities for salvage with second-line chemotherapy and stem cell transplantation in patients relapsing on the chemotherapy arm. This large study shows a relapse advantage for ASCT as postremission therapy but similar survival because more relapsing patients on the chemotherapy arm were salvaged with a late transplantation for relapse. This trial is registered at www.trialregister.nl as # NTR230 and #NTR291. (Blood. 2011;118(23):6037-6042)
引用
收藏
页码:6037 / 6042
页数:6
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