The purpose of this study is to assess pegfilgrastim starting with the first cycle versus secondary prophylaxis on neutropenic events (including neutropenia +/- fever, dose delays, dose reductions, and hospitalizations) in older patients receiving chemotherapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
852
Commercial pegfilgrastim 6mg single subcutaneous fixed-dose
Incidence of febrile neutropenia, defined by ANC < 1.0 x 10^9/L and temperature ≥ 38o C on the same day
Time frame: End of the last cycle of chemotherapy or the date of early termination from the study
Incidence of grade 3 and 4 neutropenia
Time frame: End of the last cycle of chemotherapy or the date of early termination from the study
Dose delays or dose reductions
Time frame: End of the last cycle of chemotherapy or the date of early termination from the study
Incidence of febrile neutropenia with a more strict definition (ANC < 0.5 x 10^9/L and temperature ≥ 38o C), on the same day
Time frame: End of the last cycle of chemotherapy or the date of early termination from the study
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