Stem cell transplantation-harnessing of graft-versus-malignancy

被引:7
作者
Antin, JH [1 ]
机构
[1] Harvard Univ, Sch Med,Stem Cell Transplantat Program, Dana Farber Canc Inst,Dept Med, Brigham & Womens Hosp,Div Med Oncol & Hematol, Boston, MA 02115 USA
关键词
stem cells; graft-versus-malignancy effect; allogeneic transplantation;
D O I
10.1097/00062752-200311000-00008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Allogeneic transplantation can cure a number of hematologic malignancies; however, the cost in morbidity and mortality is high. Much of the toxicity is a direct consequence of the intensity of the conditioning regimen. It has gradually been recognized that the conditioning regimen is important but not critical for the success of transplantation, particularly in the less aggressive hematologic malignancies. The graft-versus-malignancy effect, that is, the recognition of residual cancer cells by the T cells of the donor, is a critical component of the transplantation process. Recent findings This effect has been emphasized over high-dose therapy by using less intensive, and therefore less toxic conditioning regimens, thus allowing the graft-versus-malignancy effect to predominate. Reduced-intensity conditioning regimens have allowed the application of transplantation to older patients and to patients with underlying medical problems that preclude full-dose transplantation. Summary Although the long-term results of this type of approach have not yet been defined, it appears to be effective in diseases such as chronic myelogenous leukemia, chronic lymphocytic leukemia, and low-grade lymphomas that are not intrinsically very aggressive. Although the therapy appears to be valuable, concerns about delayed immune reconstitution and graft-versus-host disease remain.
引用
收藏
页码:440 / 444
页数:5
相关论文
共 44 条
[31]   Nonmyeloablative allogeneic stem cell transplantation for the treatment of chronic myeloid leukemia in first chronic phase [J].
Or, R ;
Shapira, MY ;
Resnick, I ;
Amar, A ;
Ackerstein, A ;
Samuel, S ;
Aker, M ;
Naparstek, E ;
Nagler, A ;
Slavin, S .
BLOOD, 2003, 101 (02) :441-445
[32]   INFUSIONS OF DONOR LEUKOCYTES TO TREAT EPSTEIN-BARR VIRUS-ASSOCIATED LYMPHOPROLIFERATIVE DISORDERS AFTER ALLOGENEIC BONE-MARROW TRANSPLANTATION [J].
PAPADOPOULOS, EB ;
LADANYI, M ;
EMANUEL, D ;
MACKINNON, S ;
BOULAD, F ;
CARABASI, MH ;
CASTROMALASPINA, H ;
CHILDS, BH ;
GILLIO, AP ;
SMALL, TN ;
YOUNG, JW ;
KERNAN, NA ;
OREILLY, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (17) :1185-1191
[33]   Allogeneic stem cell transplantation in the myelodysplastic syndromes: interim results of outcome following reduced-intensity conditioning compared with standard preparative regimens [J].
Parker, JE ;
Shafi, T ;
Pagliuca, A ;
Mijovic, A ;
Devereux, S ;
Potter, M ;
Prentice, HG ;
Garg, M ;
Yin, JA ;
Byrne, J ;
Russell, NH ;
Mufti, GJ .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 119 (01) :144-154
[34]  
PORTER D, 1997, APHERESIS PRINCIPLES, P501
[35]   Graft-versus-tumor induction with donor leukocyte infusions as primary therapy for patients with malignancies [J].
Porter, DL ;
Connors, JM ;
Van Deerlin, VMD ;
Duffy, KM ;
McGarigle, C ;
Saidman, SL ;
Leonard, DGB ;
Antin, JH .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1234-1243
[36]   Allogeneic cell therapy for patients who relapse after autologous stem cell transplantation [J].
Porter, DL ;
Luger, SM ;
Duffy, KM ;
Stadtmauer, EA ;
Laport, G ;
Schuster, SJ ;
Orloff, G ;
Tsai, D ;
McDaid, K ;
Kathakali, A ;
Leonard, DGB ;
Antin, JH .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2001, 7 (04) :230-238
[37]   INDUCTION OF GRAFT-VERSUS-HOST DISEASE AS IMMUNOTHERAPY FOR RELAPSED CHRONIC MYELOID-LEUKEMIA [J].
PORTER, DL ;
ROTH, MS ;
MCGARIGLE, C ;
FERRARA, JLM ;
ANTIN, JH .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (02) :100-106
[38]   Nonmyeloablative transplantation in children - Current status and future prospects [J].
Pulsipher, MA ;
Woolfrey, A .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2001, 15 (05) :809-+
[39]   Chemoresistant or aggressive lymphoma predicts for a poor outcome following reduced-intensity allogeneic progenitor cell transplantation: an analysis from the Lymphoma Working Party of the European Group for Blood and Bone Marrow Transplantation [J].
Robinson, SP ;
Goldstone, AH ;
Mackinnon, S ;
Carella, A ;
Russell, N ;
de Elvira, CR ;
Taghipour, G ;
Schmitz, N .
BLOOD, 2002, 100 (13) :4310-4316
[40]  
Robinson SP, 2002, BLOOD, V100, p144A