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Prognostic evaluation of febrile neutropenia in apparently stable adult cancer patients

BACKGROUND: Predictive models to identify low-risk febrile neutropenia (FN) have been developed with heterogeneous samples, which included stable and unstable patients, solid tumours, acute leukaemia and bone marrow transplantation. These models fail to recognise 5–15% of cases with unexpected compl...

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Autores principales: Carmona-Bayonas, A, Gómez, J, González-Billalabeitia, E, Canteras, M, Navarrete, A, Gonzálvez, M L, Vicente, V, Ayala de la Peña, F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3188929/
https://www.ncbi.nlm.nih.gov/pubmed/21811253
http://dx.doi.org/10.1038/bjc.2011.284
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author Carmona-Bayonas, A
Gómez, J
González-Billalabeitia, E
Canteras, M
Navarrete, A
Gonzálvez, M L
Vicente, V
Ayala de la Peña, F
author_facet Carmona-Bayonas, A
Gómez, J
González-Billalabeitia, E
Canteras, M
Navarrete, A
Gonzálvez, M L
Vicente, V
Ayala de la Peña, F
author_sort Carmona-Bayonas, A
collection PubMed
description BACKGROUND: Predictive models to identify low-risk febrile neutropenia (FN) have been developed with heterogeneous samples, which included stable and unstable patients, solid tumours, acute leukaemia and bone marrow transplantation. These models fail to recognise 5–15% of cases with unexpected complications, and literature specifically addressing apparently stable patients (ASPs) is scarce. METHODS: We reviewed 861 episodes of FN in outpatients with solid tumours, including 692 (80%) episodes with apparent clinical stability. We aimed to investigate the prognosis of this latter group and explore the possibility of stratifying it according to the presenting features. A case–control study was performed and the MASCC index was evaluated. RESULTS: The rates of complications and bacteraemia in ASPs were 7.3% and 6.2%, respectively. The MASCC index yielded a low sensitivity to detect complications (36%). Prognostic factors were identified: ECOG performance status ⩾2, chronic bronchitis, chronic heart failure, stomatitis NCI grade ⩾2, monocytes <200 mm(−3) and stress hyperglycaemia. CONCLUSION: A very simple assessment is useful to classify the patients with FN according to the risk of complications. A few additional variables may predict the clinical course of the patients. We additionally show that the MASCC index applied to this specific group has a low sensitivity to predict complications.
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spelling pubmed-31889292012-08-23 Prognostic evaluation of febrile neutropenia in apparently stable adult cancer patients Carmona-Bayonas, A Gómez, J González-Billalabeitia, E Canteras, M Navarrete, A Gonzálvez, M L Vicente, V Ayala de la Peña, F Br J Cancer Clinical Study BACKGROUND: Predictive models to identify low-risk febrile neutropenia (FN) have been developed with heterogeneous samples, which included stable and unstable patients, solid tumours, acute leukaemia and bone marrow transplantation. These models fail to recognise 5–15% of cases with unexpected complications, and literature specifically addressing apparently stable patients (ASPs) is scarce. METHODS: We reviewed 861 episodes of FN in outpatients with solid tumours, including 692 (80%) episodes with apparent clinical stability. We aimed to investigate the prognosis of this latter group and explore the possibility of stratifying it according to the presenting features. A case–control study was performed and the MASCC index was evaluated. RESULTS: The rates of complications and bacteraemia in ASPs were 7.3% and 6.2%, respectively. The MASCC index yielded a low sensitivity to detect complications (36%). Prognostic factors were identified: ECOG performance status ⩾2, chronic bronchitis, chronic heart failure, stomatitis NCI grade ⩾2, monocytes <200 mm(−3) and stress hyperglycaemia. CONCLUSION: A very simple assessment is useful to classify the patients with FN according to the risk of complications. A few additional variables may predict the clinical course of the patients. We additionally show that the MASCC index applied to this specific group has a low sensitivity to predict complications. Nature Publishing Group 2011-08-23 2011-08-02 /pmc/articles/PMC3188929/ /pubmed/21811253 http://dx.doi.org/10.1038/bjc.2011.284 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical Study
Carmona-Bayonas, A
Gómez, J
González-Billalabeitia, E
Canteras, M
Navarrete, A
Gonzálvez, M L
Vicente, V
Ayala de la Peña, F
Prognostic evaluation of febrile neutropenia in apparently stable adult cancer patients
title Prognostic evaluation of febrile neutropenia in apparently stable adult cancer patients
title_full Prognostic evaluation of febrile neutropenia in apparently stable adult cancer patients
title_fullStr Prognostic evaluation of febrile neutropenia in apparently stable adult cancer patients
title_full_unstemmed Prognostic evaluation of febrile neutropenia in apparently stable adult cancer patients
title_short Prognostic evaluation of febrile neutropenia in apparently stable adult cancer patients
title_sort prognostic evaluation of febrile neutropenia in apparently stable adult cancer patients
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3188929/
https://www.ncbi.nlm.nih.gov/pubmed/21811253
http://dx.doi.org/10.1038/bjc.2011.284
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