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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
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 1193154
Author(s) Pettengell, Ruth; Bosly, André; Szucs, Thomas D; Jackisch, Christian; Leonard, Robert; Paridaens, Robert; Constenla, Manuel; Schwenkglenks, Matthias; Impact of Neutropenia in Chemotherapy-European Study Group (INC-EU)
Author(s) at UniBasel Schwenkglenks, Matthias
Year 2009
Title Multivariate analysis of febrile neutropenia occurrence in patients with non-Hodgkin lymphoma : data from the INC-EU Prospective Observational European Neutropenia Study
Journal British journal of haematology : the official journal of the British Society for Haematology and the European Haematology Association
Volume 144
Number 5
Pages / Article-Number 677-85
Keywords Non-Hodgkin lymphoma, neutropenia, chemotherapy, risk factors
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.
Publisher Wiley-Blackwell
ISSN/ISBN 0007-1048
edoc-URL http://edoc.unibas.ch/dok/A6003402
Full Text on edoc No
Digital Object Identifier DOI 10.1111/j.1365-2141.2008.07514.x
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/19055662
ISI-Number WOS:000262826400006
Document type (ISI) Journal Article, Multicenter Study
 
   

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