man granulocyte colony-stimulating factor (G-CSF) is ef-fective in increasing neutrophil counts in patients with hairy cell leukemia and neutropenia. Design: Open label, phase I/II study of G-CSF, given by daily subcutaneous injection for up to 7 weeks. Setting: Outpatient oncology clinic of a university medical center. Patients: A consecutive sample of four patients with hairy cell leukemia complicated by severe neutropenia. Three pa-tients completed the study; one patient was removed after 2 weeks of therapy. Interventions: Granulocyte colony-stimulating factor was given by daily subcutaneous injection. Each patient began therapy with 1 jug/kg body weight • d; after 1 week the dose was increased to 3 jug/kg. d, and 1 week later to 6 fig/ ...
Background; Rh GM-CSF is known to stimulate the growth of granulocyte-macrophage pre- cursors and ca...
Objectives: Prophylaxis with granulocyte colony-stimulating factor (G-CSF) reduces the severity of c...
Presented in part at the 35th American Society of Clinical Oncology meeting. Atlanta (GA); 1999. Cl...
After informed consent, 86 patients with advanced cancer undergoing potentially myelosuppressive cyt...
Background: Colony stimulating factor(CSF) has been shown to accelerate neutrophil recovery after ch...
Abstract. Neutropenia is a significant dose-limiting toxicity of cancer chemotherapy, espe-cially in...
Neutropenia and subsequent susceptibility to infection are the major side effects of cytotoxic chemo...
Neutropenia is a significant dose-limiting toxicity of cancer chemotherapy, especially in dose-inten...
Chemotherapy-induced neutropenia is a major cause of morbidity and mortality. It frequently causes d...
Background: Febrile neutropenia (FN) remains one of the most challenging problems in medical oncolog...
In this study, nine patients with non-Hodgkin's lymphoma (n=6) and Hodgkin's disease (n=3) receiving...
Objectives: The degree and duration of neutropenia are crucial prognostic factors in hematological p...
Background Intensification chemotherapy improves the prognosis for children with acute lymphoblasti...
From March 1994 to January 2001, 15 courses of granulocyte transfusion (GTX) were administered to 13...
Recombinant human granulocyte colony-stimulating factor (rhG-CSF) was administered at a dose of 1-60...
Background; Rh GM-CSF is known to stimulate the growth of granulocyte-macrophage pre- cursors and ca...
Objectives: Prophylaxis with granulocyte colony-stimulating factor (G-CSF) reduces the severity of c...
Presented in part at the 35th American Society of Clinical Oncology meeting. Atlanta (GA); 1999. Cl...
After informed consent, 86 patients with advanced cancer undergoing potentially myelosuppressive cyt...
Background: Colony stimulating factor(CSF) has been shown to accelerate neutrophil recovery after ch...
Abstract. Neutropenia is a significant dose-limiting toxicity of cancer chemotherapy, espe-cially in...
Neutropenia and subsequent susceptibility to infection are the major side effects of cytotoxic chemo...
Neutropenia is a significant dose-limiting toxicity of cancer chemotherapy, especially in dose-inten...
Chemotherapy-induced neutropenia is a major cause of morbidity and mortality. It frequently causes d...
Background: Febrile neutropenia (FN) remains one of the most challenging problems in medical oncolog...
In this study, nine patients with non-Hodgkin's lymphoma (n=6) and Hodgkin's disease (n=3) receiving...
Objectives: The degree and duration of neutropenia are crucial prognostic factors in hematological p...
Background Intensification chemotherapy improves the prognosis for children with acute lymphoblasti...
From March 1994 to January 2001, 15 courses of granulocyte transfusion (GTX) were administered to 13...
Recombinant human granulocyte colony-stimulating factor (rhG-CSF) was administered at a dose of 1-60...
Background; Rh GM-CSF is known to stimulate the growth of granulocyte-macrophage pre- cursors and ca...
Objectives: Prophylaxis with granulocyte colony-stimulating factor (G-CSF) reduces the severity of c...
Presented in part at the 35th American Society of Clinical Oncology meeting. Atlanta (GA); 1999. Cl...