TY - JOUR
T1 - Bone pain associated with once-per-cycle pegfilgrastim is similar to daily filgrastim in patients with breast cancer
AU - Kubista, Ernst
AU - Glaspy, John
AU - Holmes, Frankie Ann
AU - Green, Michael D.
AU - Hackett, James
AU - Neumann, Theresa
AU - Marques, Franklin
AU - Meza, Luis
AU - Miles, David
AU - Moore, Melvin
AU - O'Shaughnessy, Joyce
AU - Piccart, Martine J.
AU - Richardson, Gary E.
AU - Samonigg, Hellmutt
AU - Santoro, Armando
AU - Savin, Michael
AU - Schaafsma, Martin Ronald
AU - Siena, Salvatore
AU - Shogan, Jeffrey
AU - Vukelja, Svetislava
AU - Wiznitzer, Israel
N1 - Funding Information:
This study was supported by Amgen Inc, Thousand Oaks, CA. We thank the research nurses and the patients who participated in this study. Martine Brassard, PhD, Wal Zani, PhD, Jennifer Renwick, BPharm, John Breddy, MSc, L. Robert Hill, PhD, and Jose L. Pico, MD, assisted with these studies. MaryAnn Foote, PhD, assisted with the writing of this article.
PY - 2003/2
Y1 - 2003/2
N2 - Bone pain is a common side effect of treatment with filgrastim. Pegfilgrastim is a pegylated long-acting analogue of filgrastim that is administered once per chemotherapy cycle. The profile of prospectively defined, patient-reported bone pain judged by the investigators as related to study drug was analyzed retrospectively for each drug using data from two comparable phase III trials. These multicenter, randomized, double-blind, noninferiority trials compared once-per-cycle pegfilgrastim (6 mg, study 1 or 100 μg/kg, study 2) to daily filgrastim 5 μg/kg in patients with stage II-IV breast cancer undergoing multiple cycles of myelosuppressive chemotherapy (doxorubicin/docetaxel). Subcutaneous once-per-cycle pegfilgrastim 6-mg and 100-μg/kg doses were administered to 76 and 150 patients, respectively; subcutaneous daily filgrastim 5 μg/kg was administered to a total of 227 patients. Because bone pain in study 1 was higher (P = 0.044) in every cycle compared with study 2, all analyses were performed separately for each study. No statistically significant differences in incidence, severity, or duration were observed between patients receiving either once-per-cycle pegfilgrastim or daily filgrastim in either study. Bone pain incidence and severity were significantly greater (P < 0.001) in cycle 1 of both studies compared with later cycles. Among patients with bone pain, a trend towards earlier onset with pegfilgrastim was observed but was not associated with increased bone pain severity or duration. In patients who received a fixed 6-mg dose of pegfilgrastim, the overall bone pain incidence was similar when analyzed by body weight (< 60 kg, 60-100 kg, > 100 kg). No patients were withdrawn from either study for bone pain.
AB - Bone pain is a common side effect of treatment with filgrastim. Pegfilgrastim is a pegylated long-acting analogue of filgrastim that is administered once per chemotherapy cycle. The profile of prospectively defined, patient-reported bone pain judged by the investigators as related to study drug was analyzed retrospectively for each drug using data from two comparable phase III trials. These multicenter, randomized, double-blind, noninferiority trials compared once-per-cycle pegfilgrastim (6 mg, study 1 or 100 μg/kg, study 2) to daily filgrastim 5 μg/kg in patients with stage II-IV breast cancer undergoing multiple cycles of myelosuppressive chemotherapy (doxorubicin/docetaxel). Subcutaneous once-per-cycle pegfilgrastim 6-mg and 100-μg/kg doses were administered to 76 and 150 patients, respectively; subcutaneous daily filgrastim 5 μg/kg was administered to a total of 227 patients. Because bone pain in study 1 was higher (P = 0.044) in every cycle compared with study 2, all analyses were performed separately for each study. No statistically significant differences in incidence, severity, or duration were observed between patients receiving either once-per-cycle pegfilgrastim or daily filgrastim in either study. Bone pain incidence and severity were significantly greater (P < 0.001) in cycle 1 of both studies compared with later cycles. Among patients with bone pain, a trend towards earlier onset with pegfilgrastim was observed but was not associated with increased bone pain severity or duration. In patients who received a fixed 6-mg dose of pegfilgrastim, the overall bone pain incidence was similar when analyzed by body weight (< 60 kg, 60-100 kg, > 100 kg). No patients were withdrawn from either study for bone pain.
KW - Fixed-weight dosing
KW - Neutrophil growth factor
KW - Phase III clinical trial
KW - Retrospective analysis
UR - http://www.scopus.com/inward/record.url?scp=0037301718&partnerID=8YFLogxK
U2 - 10.3816/CBC.2003.n.003
DO - 10.3816/CBC.2003.n.003
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AN - SCOPUS:0037301718
SN - 1526-8209
VL - 3
SP - 391
EP - 398
JO - Clinical Breast Cancer
JF - Clinical Breast Cancer
IS - 6
ER -