A prospective, real-world, multinational study of febrile neutropenia (FN) occurrence in oncology patients receiving chemotherapy with intermediate risk of FN: a MASCC Neutropenia, Infection, and Myelosuppression Study Group initiative

Purpose: Limited knowledge is available on the incidence of febrile neutropenia (FN) in intermediate-risk patients and the rationale for use of granulocyte colony-stimulating factor (G-CSF) in these patients. We aimed to estimate the rate at which patients associated with intermediate risk (10-20%)...

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Detalles Bibliográficos
Autores: Leon Rapoport, B., Garcia-Morillo, M., Font, C., Samoon, Z., Jabbar, A.A., Kourie, H.R., Kayumba, A., Esposito, F., Popescu, R.A., García. Gómez, Jesús, Heyman, L., Smit, T., Krendyukov, A., Mathieson, N., Cooksley, T., Anderson, R., Klastersky, J.
Tipo de recurso: artículo
Fecha de publicación:2023
País:España
Institución:Servizo Galego de Saúde (SERGAS)
Repositorio:RUNA. Repositorio da Consellería de Sanidade e Sergas
OAI Identifier:oai:runa.sergas.gal:20.500.11940/20999
Acceso en línea:https://portalcientifico.sergas.gal//documentos/6550da4c92517a5a7db95456
http://hdl.handle.net/20.500.11940/20999
Access Level:acceso abierto
Palabra clave:Humans
Middle Aged
Prospective Studies
Neoplasms
Granulocyte Colony-Stimulating Factor
Medical Oncology
Febrile Neutropenia
Antineoplastic Combined Chemotherapy Protocols
AS Ourense
CHUO
Descripción
Sumario:Purpose: Limited knowledge is available on the incidence of febrile neutropenia (FN) in intermediate-risk patients and the rationale for use of granulocyte colony-stimulating factor (G-CSF) in these patients. We aimed to estimate the rate at which patients associated with intermediate risk (10-20%) of FN would develop ? 1 episode of FN with a commonly used chemotherapy regimen in clinical practice. Methods: This prospective, real-world, observational, multinational, multicenter study (December 2016-October 2019) recruited patients with solid tumors or Hodgkin's/non-Hodgkin's lymphoma. Patients receiving chemotherapy with intermediate risk of FN, but not G-CSF as primary prophylaxis were included and observed for the duration of the chemotherapy (? 6 cycles and ? 30 days after the last chemotherapy administration). Results: In total, 364 patients (median age, 56 years) with 1601 cycles of chemotherapy were included in the analysis. The incidence of FN was 5% in cycle 1, 3% in cycles 2-3, and 1% in cycles 4-6. The rate of patients with ? 1 episode of FN was 9%, and 59% of FN events were reported during cycle 1. The rate of grade 4 neutropenia in cycle 1 was 11%, and 15% of patients experienced ? 1 episode of grade 4 neutropenia. Conclusions: Overall, the incidence of FN was low, with a high incidence in cycle 1 and a decrease in the subsequent cycles. These results provide the real FN risk for common chemotherapy regimens in patients generally excluded from clinical trials. Prophylactic G-CSF in intermediate-risk patients could be considered as per clinician's judgement.