Higher mortality after allogeneic peripheral-blood transplantation compared with bone marrow in children and adolescents:: The histocompatibility and alternate stem cell source working committee of the International Bone Marrow Transplant Registry

被引:184
作者
Eapen, M
Horowitz, MM
Klein, JP
Champlin, RE
Loberiza, FR
Ringdén, O
Wagner, JE
机构
[1] Med Coll Wisconsin, IBMTR, ABMTR Stat Ctr, Hlth Policy Inst, Milwaukee, WI 53226 USA
[2] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] Karolinska Inst, Stockholm, Sweden
[4] Univ Minnesota, Sch Med, Minneapolis, MN 55455 USA
关键词
D O I
10.1200/JCO.2004.02.189
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Peripheral-blood stem cells (PBSC) may be used as an alternative to bone marrow (BM) for allogeneic transplantation. Despite lack of data on PBSC transplantation in children, there has been a change in clinical practice, with increasing numbers of children receiving PBSC allografts. Patients and Methods We compared the results of 143 PBSC and 630 BM transplants from human leukocyte antigen-identical sibling donors in children aged 8 to 20 years with acute leukemia. PBSC transplant recipients were older, and were more likely to have advanced leukemia, receive growth factors post-transplantation, and have undergone transplantation more recently. Risks of acute and chronic graft-versus-host disease (GVHD), treatment-related mortality, relapse, treatment failure (relapse or death), and overall mortality were compared using Cox proportional hazards regression to adjust for potentially confounding factors. Results Hematopoietic recovery was faster after PBSC transplantation. Risks of grade 2 to 4 acute GVHD were similar, but chronic GVHD risk was higher after PBSC transplantation (relative risk [RR], 1.85; 95% CI, 1.28 to 2.66; P = .001). In contrast to reports in adults, treatment-related mortality (RR 1.89; 95% CI 1.28 to 2.80; P = .001) treatment failure (RR,,,, 1.31, 95% CI, 1.03 to 1.68; P = .03), and mortality (RR, 1.38-1 95% CI, 1.07 to 1.79; P = .01) were higher after PBSC transplantation. Risks of relapse were similar. Conclusion These data suggest poorer outcomes after PBSC compared with BM transplantation in children after adjusting for relevant risk factors. Given the trend toward increased use of PBSC allografts in children, prospective clinical trials are required to determine their appropriate role in this group of patients.
引用
收藏
页码:4872 / 4880
页数:9
相关论文
共 36 条
[1]  
ADERLINI P, 2001, BONE MARROW TRANSPL, V27, P689
[2]  
Andersen PK, 1999, STAT MED, V18, P1489, DOI 10.1002/(SICI)1097-0258(19990630)18:12<1489::AID-SIM140>3.0.CO
[3]  
2-#
[4]  
[Anonymous], 2003, Techniques for censored and truncated data, DOI DOI 10.1007/0-387-21645-6_3
[5]   Use of granulocyte colony-stimulating factor following hematopoietic cell transplantation: Does haste make waste? [J].
Appelbaum, FR .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (03) :390-391
[6]   Granulocyte-colony stimulating factor mobilizes T helper 2-inducing dendritic cells [J].
Arpinati, M ;
Green, CL ;
Heimfeld, S ;
Heuser, JE ;
Anasetti, C .
BLOOD, 2000, 95 (08) :2484-2490
[7]  
ATKINSON K, 1990, BLOOD, V75, P2459
[8]   Allogeneic peripheral blood stem cell transplantation (PBSCT) from HLA-identical sibling donors in children with hematological diseases: a single center pilot study [J].
Benito, AI ;
Gonzalez-Vicent, M ;
Garcia, F ;
Balas, A ;
Quintero, V ;
Madero, L ;
Vicario, JL ;
Diaz, MA .
BONE MARROW TRANSPLANTATION, 2001, 28 (06) :537-543
[9]   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
[10]   Randomized trial of bone marrow versus lenograstim-primed blood cell allogeneic transplantation in patients with early-stage leukemia: A report from the Societe Francaise de Greffe de Moelle [J].
Blaise, D ;
Kuentz, M ;
Fortanier, C ;
Bourhis, JH ;
Milpied, N ;
Sutton, L ;
Jouet, JP ;
Attal, M ;
Bordigoni, P ;
Cahn, JY ;
Boiron, JM ;
Schuller, MP ;
Moatti, JP ;
Michalle, M .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (03) :537-546