The myelodysplastic syndromes are a heterogenous family of hematologic diso
rders characterized by ineffective hematopoiesis, Because of the interpatie
nt variability regarding prognosis and morbidity, management of myelodyspla
stic syndromes continues to be a challenge to clinical hematologists. Pancy
topenia and defective function of neutrophils and platelets carry a high ri
sk of infectious or hemorrhagic complications. Erythropoietin is perhaps th
e most commonly used therapeutic option, second only to transfusion; improv
ement of erythropoiesis is seen in approximately 20% of patients, mainly in
those with relatively preserved erythroid function and no or low transfusi
on requirements. Coadministration of erythropoietin with either granulocyte
colony-stimulating factor or granulocyte-macrophage colony-stimulating fac
tor may increase the response rate up to 50%. Although prophylactic adminis
tration of granulocyte- or granulocyte-macrophage colony-stimulating factor
cannot be recommended, treatment of febrile neutropenia might benefit from
administration of granulocyte- or granulocyte-macrophage colony-stimulatin
g factor in addition to antibiotics. (C) Lippincott Williams & Wilkins, Inc
.