Conventional myeloablative allogeneic hematopoietic cell transplantation pr
oduces considerable morbidity and mortality. These generally limit this tre
atment to patients in good medical condition who are younger than 55 years
of age. T-cell-mediated graft-versus-tumor effects play a key role in the e
limination of malignancy after allografting. Several investigators have sou
ght to reduce regimen-related toxicities while optimizing graft-versus-tumo
r effects. Strategies can be broadly classified as (1) reduced-intensity re
gimens that retain some toxicity, and (2) minimally myelosuppressive regime
ns that rely on immunosuppression for allogeneic engraftment and resultant
graft-versus-tumor effects. Although follow-up has been short, preliminary
results are encouraging. Current challenges include defining a regimen that
will facilitate full donor engraftment while minimizing toxicities and gra
ft-versus-host disease. If long-term efficacy is demonstrated, such strateg
ies will expand the options for patients who would not qualify for conventi
onal allogeneic transplants. (C) 2001 Lippincott Williams & Wilkins, Inc.