Novel conditioning regimens and nonmyeloablative stem cell transplants

被引:6
作者
Baker, KS [1 ]
Wagner, JE [1 ]
机构
[1] Univ Minnesota, Dept Pediat, Pediat Blood & Marrow Transplant Program, Minneapolis, MN 55455 USA
关键词
D O I
10.1097/00008480-200202000-00004
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Allogeneic stem cell transplantation has proven an effective means of treatment for a variety of malignant and nonmalignant conditions. Stem cell transplantation has traditionally been preceded by the patient receiving high (myeloablative) doses of chemotherapy and total body irradiation, which have been associated with significant transplant-related morbidity and mortality. This finding has precluded some older or heavily pretreated patients from being offered stem cell transplantation and has made other populations, such as those with nonmalignant conditions, reluctant to consider this therapy. Preclinical studies demonstrated that engraftment of donor stem cells could be achieved with nonmyeloablative, but immunosuppressive, preparative regimens that are significantly less toxic. Preliminary clinical studies have shown that patients previously ineligible for allogeneic stem cell transplantation can frequently be safely transplanted and that an immune-mediated graft-versus-malignancy effect plays an important role in the antitumor efficacy of this treatment. The potential to use this nonmyeloablative approach in nonmalignant disorders in which regimen-related toxicity must be minimized is of particular interest in children. (C) 2002 Lippincott Williams Wilkins, Inc.
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页码:17 / 22
页数:6
相关论文
共 32 条
[21]   Second allogeneic stem cell transplantation using nonmyeloablative conditioning for patients who relapsed or developed secondary malignancies following autologous transplantation [J].
Nagler, A ;
Or, R ;
Naparstek, E ;
Varadi, G ;
Slavin, S .
EXPERIMENTAL HEMATOLOGY, 2000, 28 (09) :1096-1104
[22]   Allogeneic chimerism with low-dose irradiation, antigen presensitization, and costimulator blockade in H-2 mismatched mice [J].
Quesenberry, PJ ;
Zhong, SJ ;
Wang, H ;
Stewart, M .
BLOOD, 2001, 97 (02) :557-564
[23]  
RAUBISIN M, 2000, HAEMATOLOGICA, V85, P81
[24]   Results of an outpatient-based stem cell allotransplant program using nonmyeloablative conditioning regimens [J].
Ruiz-Argüelles, GJ ;
Gómez-Almaguer, D ;
Ruiz-Argüelles, A ;
González-Llano, O ;
Cantú, OG ;
Jaime-Pérez, JC .
AMERICAN JOURNAL OF HEMATOLOGY, 2001, 66 (04) :241-244
[25]   Graft vs autoimmunity following allogeneic non-myeloablative blood stem cell transplantation in a patient with chronic myelogenous leukemia and severe systemic psoriasis and psoriatic polyarthritis [J].
Slavin, S ;
Nagler, A ;
Varadi, G ;
Or, R .
EXPERIMENTAL HEMATOLOGY, 2000, 28 (07) :853-857
[26]   Combined histocompatibility leukocyte antigen-matched donor bone marrow and renal transplantation for multiple myeloma with end stage renal disease: The induction of allograft tolerance through mixed lymphohematopoietic chimerism [J].
Spitzer, TR ;
Delmonico, F ;
Tolkoff-Rubin, N ;
McAfee, S ;
Sackstein, R ;
Saidman, S ;
Colby, C ;
Sykes, M ;
Sachs, DH ;
Cosimi A, B .
TRANSPLANTATION, 1999, 68 (04) :480-484
[27]   Intentional induction of mixed chimerism and achievement of antitumor responses after nonmyeloablative conditioning therapy and HLA-matched donor bone marrow transplantation for refractory hematologic malignancies [J].
Spitzer, TR ;
McAfee, S ;
Sackstein, R ;
Colby, C ;
Multani, P ;
Saidman, S ;
Weymouth, D ;
Preffer, F ;
Poliquin, C ;
Foley, A ;
Cox, B ;
Andrews, D ;
Sachs, DH ;
Sykes, M .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2000, 6 (3A) :309-320
[28]   Stable mixed hematopoietic chimerism in DLA-identical littermate dogs given sublethal total body irradiation before and pharmacological immunosuppression after marrow transplantation [J].
Storb, R ;
Yu, C ;
Wagner, JL ;
Deeg, HJ ;
Nash, RA ;
Kiem, HP ;
Leisenring, W ;
Shulman, H .
BLOOD, 1997, 89 (08) :3048-3054
[29]   Successful application of nonmyeloablative transplantation for paroxysmal nocturnal hemoglobinuria [J].
Suenaga, K ;
Kanda, Y ;
Niiya, H ;
Nakai, K ;
Saito, T ;
Saito, A ;
Ohnishi, M ;
Takeuchi, T ;
Tanosaki, R ;
Makimoto, A ;
Miyawaki, S ;
Ohnishi, T ;
Kanai, S ;
Tobinai, K ;
Takaue, Y ;
Mineishi, S .
EXPERIMENTAL HEMATOLOGY, 2001, 29 (05) :639-642
[30]  
Svennilson J, 2000, Pediatr Transplant, V4, P247, DOI 10.1034/j.1399-3046.2000.00029.x