UT MDAnderson Cancer Center
Houston, Texas, 77030, United States
NCT Number: NCT00283621
To determine the percentage of patients and number of cycles in which a packed red blood cell transfusion was administered due to anemia and in which antibiotics were administered due to neutropenic fever.
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Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Houston, Texas, 77030, United States
The use of hematopoietic growth factors have been shown to reduce neutropenic complications and red cell transfusion requirements associated with chemotherapy. This trial will study the combination of pegfilgrastim and darbepoetin alfa administered once per cycle of chemotherapy. Prior experience with growth factors in this setting provides historical data for comparison of safety and activity of these newer longer acting growth factors in reducing the incidence of febrile neutropenia requiring antibiotics and anemia requiring transfusions. The once dosing per cycle would simplify the patient management and would improve patient convenience and compliance.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: Doxorubicin Hydrocholoride, Adriamycin PFS, Adriamycin RDF
Other names: Ifex
Time frame: Monitored at least twice a week and daily during severe myelosuppression.
Time frame: Blood drawn at baseline during cycle 3 and at the end of study.
Time frame: Performed at baseline and post treatment.
Time frame: Assessed at baseline, after 3 cycles of treatment and at the end of the study.
M.D. Anderson Cancer Center
Other
A Pilot Study of Aranesp (Darbepoetin Alfa) and Pegfilgrastim (Neulasta) in Patients With Sarcoma Receiving Adriamycin and Ifosfamide
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