FoRMuLARy MAnAgeMenTsingle injection was required. In these patients treated with a heterogeneous group of chemotherapy regimens with a broad range of risk of FN, overall, an absolute 1.8% increase in the incidence of developing FN was observed in patients who received filgrastim compared with patients who received pegfilgrastim, (absolute rates of 6.5% and 4.7%, respectively).
What is already known about this subject• Chemotherapy-induced neutropenia is a common side effect of cancer treatment, which leaves patients vulnerable to lifethreatening infections. The risk of febrile neutropenia (FN) can vary depending on chemotherapy drug regimens and patient characteristics such as advanced age or comorbid conditions (i.e., poor renal function, diabetes). • Randomized controlled trials have shown colony-stimulating factors (CSFs) filgrastim and pegfilgrastim significantly decrease the risk of FN by half (risk reduction [RR], 0.54 in randomized controlled trials). The absolute RR reported in the clinical trials ranged from 8% to 37%, the variation reflecting differences in the base-line risk of FN associated with the chemotherapy regimen.• Head-to-head randomized controlled trials of pegfilgrastim versus filgrastim demonstrate that both drugs have similar efficacy; however, little is known about their relative effectiveness in clinical practice.
What this study adds• For the first time, data are available regarding the real-world incidence of FN in chemotherapy patients treated in the community setting with filgrastim or pegfilgrastim or both CSF agents.• In community oncology practices, patients who received filgrastim initiated treatment later and received fewer days per cycle than the timing of initiation and duration of therapy demonstrated to be effective in randomized controlled trials. In contrast, pegfilgrastim was commonly initiated within 3 days of chemotherapy.• Among patients treated with a heterogeneous group of chemotherapy regimens with a broad range of risk of FN in community oncology practices, overall, a 1.8% overall increase in the incidence of developing FN was observed in patients who received filgrastim compared with patients who received pegfilgrastim (absolute rates of 6.5% and 4.7%, respectively) resulting in a 40% increase in the odds of FN. For every 56 patients treated in community settings with pegfilgrastim instead of filgrastim, 1 additional case of FN would be avoided.BACKGROUNd: Colony-stimulating factors (CSFs) significantly decrease the risk of febrile neutropenia (FN), a common complication of myelosuppressive chemotherapy. Pegfilgrastim (6 mg), introduced in 2002, has a sustained duration of action, with a single dose comparable in efficacy to daily injections of filgrastim (5 μg per kg per day) for 10 to 11 days; both agents should be initiated 24 hours after completing chemotherapy.