Reduced intensity conditioning for allogeneic hematopoietic stem cell transplantation in patients with acute myeloid leukemia:: disease status by marrow blasts is the strongest prognostic factor

被引:120
作者
Sayer, HG
Kröger, M
Beyer, J
Kiehl, M
Klein, SA
Schaefer-Eckart, K
Schwerdtfeger, R
Siegert, W
Runde, V
Theuser, C
Martin, H
Schetelig, J
Beelen, DW
Fauser, A
Kienast, J
Höffken, K
Ehninger, G
Bornhäuser, M
机构
[1] Univ Jena, Klin & Poliklin Innere Med 2, D-07740 Jena, Germany
[2] Univ Munster, Dept Med Hematol & Oncol, D-4400 Munster, Germany
[3] Univ Marburg, Abt Hamatol Onkol & Immunol, D-35032 Marburg, Germany
[4] Klin Knochenmarktransplantat, Idar Oberstein, Germany
[5] Univ Frankfurt, Abt Hamatol Innere Med, D-6000 Frankfurt, Germany
[6] Med Klin Nurnberg, Nurnberg, Germany
[7] Deutsch Klin Diagnost Knochenmarktransplantat Wie, Wiesbaden, Germany
[8] Humboldt Univ, Champus Charite Mitte, Med Klin Hamatol & Onkol 2, D-1086 Berlin, Germany
[9] Univ Essen Gesamthsch, Klin Knochenmarktransplantat, Essen, Germany
[10] Univ Dresden, Med Klin & Poliklin 1, Dresden, Germany
关键词
acute myeloid leukemia; reduced conditioning; allogeneic stem cell transplantation;
D O I
10.1038/sj.bmt.1704062
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We analyzed predictive factors for the outcome of 113 acute myeloid leukemia patients receiving reduced-intensity conditioning prior to allogeneic hematopoietic stem cell transplantation (HSCT). Patients were ineligible for conventional-intensity HSCT. Conditioning consisted of fludarabine and 50% of the conventional dose of busulfan (n = 93) or total body irradiation (n = 20). The source of stem cells was blood in 102 patients, marrow in 10, and both in one. In total, 50 (44.2%) donors were HLA-matched siblings, 50 (44.2%) unrelated fully matched and 13 (11.5%) partially mismatched family (n 1) or unrelated (n = 12) donors. In all, 107 (94.6%) patients showed neutrophil and platelet engraftment after a median time of 13.5 and 13 days. The probabilities of event-free survival (EFS) (median follow-up: 12 months) were 49% for patients with less than 5% blasts in the marrow, 24% for patients with 5-20% blasts (P = 0.002) and 14% with >20% blasts (Pless than or equal to0.001). Death occurred because of relapse in 29 patients (25.6%), infection in 12 patients (10.6%), acute graft-versus-host disease in eight patients (7.0%) and organ toxicity in nine patients (7.9%). In multivariate analysis, higher number of blasts in the marrow, alternative donors and low Karnofsky performance score were independent adverse prognostic factors for EFS.
引用
收藏
页码:1089 / 1095
页数:7
相关论文
共 27 条
[1]  
AUER I, 1991, BONE MARROW TRANSPL, V4, P255
[2]   Transplantation of bone marrow as compared with peripheral-blood cells from HLA-identical relatives in patients with hematologic cancers. [J].
Bensinger, WI ;
Martin, PJ ;
Storer, B ;
Clift, R ;
Forman, SJ ;
Negrin, R ;
Kashyap, A ;
Flowers, MED ;
Lilleby, K ;
Chauncey, TR ;
Storb, R ;
Appelbaum, FR ;
Rowley, S ;
Heimfeld, S ;
Blume, K .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (03) :175-181
[3]   A randomized study of high-dose cytarabine in induction in acute myeloid leukemia [J].
Bishop, JF ;
Matthews, JP ;
Young, GA ;
Szer, J ;
Gillett, A ;
Joshua, D ;
Bradstock, K ;
Enno, A ;
Wolf, MM ;
Fox, R ;
Cobcroft, R ;
Herrmann, R ;
VanDerWeyden, M ;
Lowenthal, RM ;
Page, F ;
Garson, OM ;
Juneja, S .
BLOOD, 1996, 87 (05) :1710-1717
[4]  
Bornhäuser M, 2001, CLIN CANCER RES, V7, P2254
[5]   Chemotherapy compared with autologous or allogeneic bone marrow transplantation in the management of acute myeloid leukemia in first remission [J].
Cassileth, PA ;
Harrington, DP ;
Appelbaum, FR ;
Lazarus, HM ;
Rowe, JM ;
Paietta, E ;
Willman, C ;
Hurd, DD ;
Bennett, JM ;
Blume, KG ;
Head, DR ;
Wiernik, PH .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (23) :1649-1656
[6]  
CIFT R, 1990, BLOOD, V76, P1867
[7]   Reduced-intensity conditioning followed by allografting of hematopoietic cells can produce clinical and molecular remissions in patients with poor-risk hematologic malignancies [J].
Corradini, P ;
Tarella, C ;
Olivieri, A ;
Gianni, AM ;
Voena, C ;
Zallio, F ;
Ladetto, M ;
Falda, M ;
Lucesole, M ;
Dodero, A ;
Ciceri, F ;
Benedetti, F ;
Rambaldi, A ;
Sajeva, MR ;
Tresoldi, M ;
Pileri, A ;
Bordignon, C ;
Bregni, M .
BLOOD, 2002, 99 (01) :75-82
[8]  
Frassoni F, 1996, BONE MARROW TRANSPL, V17, P13
[9]   Engraftment of allogeneic hematopoietic progenitor cells with purine analog-containing chemotherapy: Harnessing graft-versus-leukemia without myeloablative therapy [J].
Giralt, S ;
Estey, E ;
Albitar, M ;
vanBesien, K ;
Rondon, G ;
Anderlini, P ;
OBrien, S ;
Khouri, I ;
Gajewski, J ;
Mehra, R ;
Claxton, D ;
Andersson, B ;
Beran, M ;
Przepiorka, D ;
Koller, C ;
Kornblau, S ;
Korbling, M ;
Keating, M ;
Kantarjian, H ;
Champlin, R .
BLOOD, 1997, 89 (12) :4531-4536
[10]   Melphalan and purine analog-containing preparative regimens: reduced-intensity conditioning for patients with hematologic malignancies undergoing allogeneic progenitor cell transplantation [J].
Giralt, S ;
Thall, PF ;
Khouri, I ;
Wang, XM ;
Braunschweig, I ;
Ippolitti, C ;
Claxton, D ;
Donato, M ;
Bruton, J ;
Cohen, A ;
Davis, M ;
Andersson, BS ;
Anderlini, P ;
Gajewski, J ;
Kornblau, S ;
Andreeff, M ;
Przepiorka, D ;
Ueno, NT ;
Molldrem, J ;
Champlin, R .
BLOOD, 2001, 97 (03) :631-637