Allogeneic hematopoietic cell transplantation in children with relapsed acute lymphoblastic leukemia isolated to the central nervous system

被引:20
作者
Harker-Murray, Paul D. [1 ]
Thomas, Avis J. [1 ]
Wagner, John E. [1 ]
Weisdorf, Daniel [2 ]
Luo, Xianghua [3 ]
DeFor, Todd E. [1 ,3 ]
Verneris, Michael R. [1 ]
Dusenbery, Kathryn E. [4 ]
MacMillan, Margaret L. [1 ]
Tolar, Jakub [1 ]
Baker, K. Scott [1 ]
Orchard, Paul J. [1 ]
机构
[1] Univ Minnesota, Med Ctr, Pediat Blood & Marrow Transplant Program, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Adult Blood & Marrow Transplant Program, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Div Biostat, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Dept Therapeut Radiol Radiat Oncol, Minneapolis, MN 55455 USA
关键词
bone marrow; graft-versus-host disease; stem cell; umbilical cord blood; acute lymphocytic leukemia; CNS relapse;
D O I
10.1016/j.bbmt.2008.03.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Allogeneic hematopoietic cell transplantation (HCT) is the standard of care for pediatric patients with early medullary relapse of acute lymphoblastic leukemia (ALL). Most patients with isolated central nervous system (CNS) relapse have good outcomes when treated with intrathecal and systemic chemotherapy followed by irradiation to the neuroaxis. However, the role of HCT remains unclear for those patients with early isolated CNS relapse (<18 months) or who had high risk disease at diagnosis. We therefore compared the HCT outcomes of 116 children treated at the University of Minnesota from 1991 to 2006 with relapsed ALL involving the CNS alone (CNS, n = 14), the bone marrow alone (BM, n = 85), or both bone marrow and CNS (BM + CNS, n = 17). There were no significant differences among groups in age at diagnosis or transplant, length of first complete remission (CR1), remission status (CR2 versus >= CR3), graft source, or preparative regimen. The incidence of acute GVHD was similar between groups. Patients with isolated CNS relapse had the lowest cumulative incidence of mortality following transplant (CNS: 0%, BM: 19%, BM + CNS: 29%, P = .03) and relapse (CNS: 0% BM: 30%, BM + CNS: 12%, at 2 years, P = .01) and highest leukemia-free survival (CNS: 91%, BM: 35%, BM + CNS: 46%, P < .01) at 5 years. Risk factors for poor survival were: T cell leukemia or BCR-ABL gene rearrangement, history of marrow relapse, and receipt of HLA-mismatched marrow. These data support the use of allogeneic HCT in the treatment of children with poor prognosis isolated CNS relapse. (C) 2008 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:685 / 692
页数:8
相关论文
共 34 条
[11]  
COX DR, 1972, J R STAT SOC B, V34, P187
[12]   Unrelated donor bone marrow transplantation for children with acute leukemia [J].
Davies, SM ;
Wagner, JE ;
Shu, XO ;
Blazar, BR ;
Katsanis, E ;
Orchard, PJ ;
Kersey, JH ;
Dusenbery, KE ;
Weisdorf, DJ ;
McGlave, PB ;
Ramsay, NKC .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (02) :557-565
[13]   Long-term effects of radiation therapy on cognitive and endocrine function in children with leukemia and brain tumors [J].
Duffner, PK .
NEUROLOGIST, 2004, 10 (06) :293-310
[14]   Outcomes after HLA-matched sibling transplantation or chemotherapy in children with B-precursor acute lymphoblastic leukemia in a second remission: a collaborative study of the Children's Oncology Group and the Center for International Blood and Marrow Transplant Research [J].
Eapen, M ;
Raetz, E ;
Zhang, MJ ;
Muehlenbein, C ;
Devidas, M ;
Abshire, T ;
Billett, A ;
Homans, A ;
Camitta, B ;
Carroll, WL ;
Davies, SM .
BLOOD, 2006, 107 (12) :4961-4967
[15]  
Gaynon PS, 1998, CANCER, V82, P1387, DOI 10.1002/(SICI)1097-0142(19980401)82:7<1387::AID-CNCR24>3.0.CO
[16]  
2-1
[17]   Intensification of therapy for children with lower-risk acute lymphoblastic leukemia: Long-term follow-up of patients treated on Children's Cancer Group trial 1881 [J].
Hutchinson, RJ ;
Gaynon, PS ;
Sather, H ;
Bertolone, SJ ;
Cooper, HA ;
Tannous, R ;
Wells, LM ;
Heerema, NA ;
Sailer, S ;
Trigg, ME .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (09) :1790-1797
[18]   COMPARISON OF AUTOLOGOUS AND ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR TREATMENT OF HIGH-RISK REFRACTORY ACUTE LYMPHOBLASTIC-LEUKEMIA [J].
KERSEY, JH ;
WEISDORF, D ;
NESBIT, ME ;
LEBIEN, TW ;
WOODS, WG ;
MCGLAVE, PB ;
KIM, T ;
VALLERA, DA ;
GOLDMAN, AI ;
BOSTROM, B ;
HURD, D ;
RAMSAY, NKC .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (08) :461-467
[19]   COMPARISON OF 2 TOTAL-BODY IRRADIATION REGIMENS IN ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR ACUTE NONLYMPHOBLASTIC LEUKEMIA IN 1ST REMISSION [J].
KIM, TH ;
MCGLAVE, PB ;
RAMSAY, N ;
WOODS, W ;
BOSTROM, B ;
VERCELLOTTI, G ;
HURD, D ;
KRIVIT, W ;
NESBIT, M ;
HAAKE, R ;
KHAN, F ;
KERSEY, JH .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1990, 19 (04) :889-897
[20]   Double-delayed intensification improves event-free survival for children with intermediate-risk acute lymphoblastic leukemia: a report from the Children's Cancer Group [J].
Lange, BJ ;
Bostrom, BC ;
Cherlow, JM ;
Sensel, MG ;
La, MKL ;
Rackoff, W ;
Heerema, NA ;
Wimmer, RS ;
Trigg, ME ;
Sather, HN .
BLOOD, 2002, 99 (03) :825-833