Pegfilgrastim administration after 24 or 72 or 96 h to allow dose-dense anthracycline- and taxane-based chemotherapy in breast cancer patients: a single-center experience within the GIM2 randomized phase III trial
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作者单位:Matteo Lambertini (1) Paolo Bruzzi (2) Francesca Poggio (1) Simona Pastorino (1) Giovanni Gardin (1) Matteo Clavarezza (3) Claudia Bighin (1) Paolo Pronzato (1) Lucia Del Mastro (4)
1. Department of Medical Oncology, U.O. Oncologia Medica 2, IRCCS AOU San Martino-IST, Largo Rosanna Benzi, 10, 16132, Genova, Italy 2. Department of Epidemiology, IRCCS AOU San Martino-IST, Genova, Italy 3. Department of Medical Oncology, U.O. Oncologia Medica, Ospedali Galliera, Genova, Italy 4. Department of Medical Oncology, U.O. Sviluppo Terapie Innovative, IRCCS AOU San Martino-IST, Genova, Italy
刊物类别:Medicine
刊物主题:Medicine & Public Health Oncology Nursing Nursing Management and Research Pain Medicine Rehabilitation Medicine
出版者:Springer Berlin / Heidelberg
ISSN:1433-7339
文摘
Purpose To evaluate the safest timing of pegfilgrastim administration in dose-dense anthracycline- and taxane-based chemotherapy, three different cohorts of patients enrolled in the Gruppo Italiano Mammella (GIM) 2 study and treated at the coordinating center received pegfilgrastim 24 h (cohort A) or 72 h (cohort B) or 96 h (cohort C) after chemotherapy.