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Multivariate analysis of febrile neutropenia occurrence in patients with non-Hodgkin lymphoma: data from the INC-EU Prospective Observational European Neutropenia Study
Authors:Ruth Pettengell,ré   Bosly,Thomas D. Szucs,Christian Jackisch,Robert Leonard,Robert Paridaens,Manuel Constenla, Matthias Schwenkglenks,for the Impact of Neutropenia in Chemotherapy - European Study Group
Affiliation:Cellular and Molecular Medicine, St George's University of London, Cranmer Terrace, London, UK;, Service d'Hématologie, Cliniques Universitaires UCL, Godinne, Belgium;, European Centre of Pharmaceutical Medicine, University of Basel, c/o ECPM Executive Office, University Hospital, Basel, Switzerland;, Department of Gynaecology and Obstetrics, Klinikum Offenbach, Offenbach, Germany;, Cancer Services &Clinical Haematology, Charing Cross Hospital, London, UK;, Department of Medical Oncology, University Hospital Gasthuisberg, Leuven, Belgium;, and Servicio de Oncologia, Complexo Hospitalario de Pontevedra, Pontevedra, Spain
Abstract:Myelosuppression, particularly febrile neutropenia (FN), are serious dose-limiting toxicities that occur frequently during the first cycle of chemotherapy. Identifying patients most at risk of developing FN might help physicians to target prophylactic treatment with colony-stimulating factor (CSF), in order to decrease the incidence, or duration, of myelosuppression and facilitate delivery of chemotherapy as planned. We present a risk model for FN occurrence in the first cycle of chemotherapy, based on a subgroup of 240 patients with non-Hodgkin lymphoma (NHL) enroled in our European prospective observational study. Eligible patients had an International Prognostic Index of 0–3, and were scheduled to receive a new myelosuppressive chemotherapy regimen with at least four cycles. Clinically relevant factors significantly associated with cycle 1 FN were older age, increasing planned cyclophosphamide dose, a history of previous chemotherapy, a history of recent infection, and low baseline albumin (<35 g/l). Prophylactic CSF use and higher weight were associated with a significant protective effect. The model had high sensitivity (81%) and specificity (80%). Our model, together with treatment guidelines, may rationalise the clinical decision of whether to support patients with CSF primary prophylaxis based on their risk factor profile. Further validation is required.
Keywords:Non-Hodgkin lymphoma    neutropenia    chemotherapy    risk factors
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