Intravenous busulfan for autologous stem cell transplantation in adult patients with acute myeloid leukemia: a survey of 952 patients on behalf of the Acute Leukemia Working Party of the European Group for Blood and Marrow Transplantation

被引:29
|
作者
Nagler, Arnon [1 ]
Labopin, Myriam [2 ]
Gorin, Norbert-Claude [2 ,3 ]
Ferrara, Felicetto [4 ]
Sanz, Miguel A. [5 ]
Wu, Depei [6 ]
Torres Gomez, Antonio [7 ]
Lapusan, Simona [3 ]
Irrera, Giuseppe [8 ]
Guimaraes, Jose E. [9 ,10 ]
Sousa, Aida Botelho [11 ]
Carella, Angelo M. [12 ]
Vey, Norbert [13 ]
Arcese, William [14 ]
Shimoni, Avichai [1 ]
Berger, Raanan [1 ]
Rocha, Vanderson [15 ]
Mohty, Mohamad [2 ,3 ]
机构
[1] Chaim Sheba Med Ctr, IL-52621 Tel Hashomer, Israel
[2] Univ Paris 06, Hop St Antoine, AP HP, Acute Leukemia Working Party EBMT,INSERM UMR S 93, Paris, France
[3] Hop St Antoine, Dept Hematol & Cell Therapy, F-75571 Paris, France
[4] Cardarelli Hosp, Naples, Italy
[5] Univ Valencia, Hosp Univ La Fe, E-46003 Valencia, Spain
[6] Soochow Univ, Affiliated Hosp 1, Suzhou, Peoples R China
[7] Hosp Reina Sofia, Cordoba, Spain
[8] Azienda Osped, Reggio Di Calabria, Italy
[9] Hosp Sao Joao, Oporto, Portugal
[10] Sch Med, Oporto, Portugal
[11] Hosp Capuchos, Lisbon, Portugal
[12] Hosp San Martino, Genoa, Italy
[13] Ctr Paoli Calmettes, Marseille, France
[14] Rome Transplant Network, Rome, Italy
[15] Univ Oxford, Churchill Hosp, Oxford OX1 2JD, England
关键词
ACUTE MYELOCYTIC-LEUKEMIA; ACUTE MYELOGENOUS LEUKEMIA; 1ST COMPLETE REMISSION; PEDIATRIC-PATIENTS; INTENSIVE CHEMOTHERAPY; VENOOCCLUSIVE DISEASE; CONDITIONING REGIMEN; CYCLOPHOSPHAMIDE CY; GRAFT-REJECTION; IV BUSULFAN;
D O I
10.3324/haematol.2014.105197
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Oral busulfan is the historical backbone of the busulfan+cyclophosphamide regimen for autologous stem cell transplantation. However intravenous busulfan has more predictable pharmacokinetics and less toxicity than oral busulfan; we, therefore, retrospectively analyzed data from 952 patients with acute myeloid leukemia who received intravenous busulfan for autologous stem cell transplantation. Most patients were male (n=531, 56%), and the median age at transplantation was 50.5 years. Two-year overall survival, leukemia-free survival, and relapse incidence were 67 +/- 2%, 53 +/- 2%, and 40 +/- 2%, respectively. The non-relapse mortality rate at 2 years was 7 +/- 1%. Five patients died from veno-occlusive disease. Overall leukemia-free survival and relapse incidence at 2 years did not differ significantly between the 815 patients transplanted in first complete remission (52 +/- 2% and 40 +/- 2%, respectively) and the 137 patients transplanted in second complete remission (58 +/- 5% and 35 +/- 5%, respectively). Cytogenetic risk classification and age were significant prognostic factors: the 2-year leukemia-free survival was 63 +/- 4% in patients with good risk cytogenetics, 52 +/- 3% in those with intermediate risk cytogenetics, and 37 +/- 10% in those with poor risk cytogenetics (P=0.01); patients <= 50 years old had better overall survival (77 +/- 2% versus 56 +/- 3%; P<0.001), leukemia-free survival (61 +/- 3% versus 45 +/- 3%; P<0.001), relapse incidence (35 +/- 2% versus 45 +/- 3%; P<0.005), and non-relapse mortality (4 +/- 1% versus 10 +/- 2%; P<0.001) than older patients. The combination of intravenous busulfan and high-dose melphalan was associated with the best overall survival (75 +/- 4%). Our results suggest that the use of intravenous busulfan simplifies the autograft procedure and confirm the usefulness of autologous stem cell transplantation in acute myeloid leukemia. As in allogeneic transplantation, veno-occlusive disease is an uncommon complication after an autograft using intravenous busulfan.
引用
收藏
页码:1380 / 1386
页数:7
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