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A multi-centre study comparing granulocyte-colony stimulating factors to antibiotics for primary prophylaxis of docetaxel-cyclophosphamide induced febrile neutropenia

BACKGROUND: Primary febrile neutropenia (FN) prophylaxis with ciprofloxacin or granulocyte-colony stimulating factors (G-CSF) is recommended with docetaxel-cyclophosphamide (TC) chemotherapy for early-stage breast cancer (EBC). A pragmatic randomised trial compared the superiority of G-CSF to ciprof...

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Autores principales: Clemons, Mark, Fergusson, Dean, Joy, Anil A., Thavorn, Kednapa, Meza-Junco, Judith, Hiller, Julie Price, Mackey, John, Ng, Terry, Zhu, Xiaofu, Ibrahim, Mohammed F.K., Sienkiewicz, Marta, Saunders, Deanna, Vandermeer, Lisa, Pond, Gregory, Basulaiman, Bassam, Awan, Arif, Pitre, Lacey, Nixon, Nancy A., Hutton, Brian, Hilton, John F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8095051/
https://www.ncbi.nlm.nih.gov/pubmed/33901921
http://dx.doi.org/10.1016/j.breast.2021.03.012
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author Clemons, Mark
Fergusson, Dean
Joy, Anil A.
Thavorn, Kednapa
Meza-Junco, Judith
Hiller, Julie Price
Mackey, John
Ng, Terry
Zhu, Xiaofu
Ibrahim, Mohammed F.K.
Sienkiewicz, Marta
Saunders, Deanna
Vandermeer, Lisa
Pond, Gregory
Basulaiman, Bassam
Awan, Arif
Pitre, Lacey
Nixon, Nancy A.
Hutton, Brian
Hilton, John F.
author_facet Clemons, Mark
Fergusson, Dean
Joy, Anil A.
Thavorn, Kednapa
Meza-Junco, Judith
Hiller, Julie Price
Mackey, John
Ng, Terry
Zhu, Xiaofu
Ibrahim, Mohammed F.K.
Sienkiewicz, Marta
Saunders, Deanna
Vandermeer, Lisa
Pond, Gregory
Basulaiman, Bassam
Awan, Arif
Pitre, Lacey
Nixon, Nancy A.
Hutton, Brian
Hilton, John F.
author_sort Clemons, Mark
collection PubMed
description BACKGROUND: Primary febrile neutropenia (FN) prophylaxis with ciprofloxacin or granulocyte-colony stimulating factors (G-CSF) is recommended with docetaxel-cyclophosphamide (TC) chemotherapy for early-stage breast cancer (EBC). A pragmatic randomised trial compared the superiority of G-CSF to ciprofloxacin and a cost-utility analysis were conducted. METHODS: EBC patients receiving TC chemotherapy were randomised to ciprofloxacin or G-CSF. The primary outcome was a composite of FN and non-FN treatment-related hospitalisation. Secondary outcomes included; rates of FN, non-FN treatment-related hospitalisation, chemotherapy dose reductions/delays/discontinuations. Primary analysis was performed with the intention to treat population. Cost-utility analyses were conducted from the Canadian public payer perspective. RESULTS: 458 eligible patients were randomised: 228 to ciprofloxacin and 230 to G-CSF. For the primary endpoint there was non-statistically significant difference (Risk difference = −6.7%, 95%CI = −13.5%–0.1%, p = 0.061) between ciprofloxacin patients (46,20.2%) and G-CSF (31,13.5%). Patients receiving ciprofloxacin were more likely to experience FN (36/228, 15.8% vs 13/230, 5.7%) than patients receiving G-CSF (p < 0.001). Non-FN treatment-related hospitalisation occurred in 40/228 (17.5%) of ciprofloxacin patients vs 28/230 (12.2%) of G-CSF patients (p = 0.12). There were no differences in other secondary outcomes. G-CSF was associated with an incremental cost-effectiveness ratio of C$1,760,796 per one quality-adjusted life year gained. CONCLUSION: The primary endpoint of superiority of G-CSF over ciprofloxacin was not demonstrated. While there were reduced FN rates with G-CSF, there were no differences in chemotherapy dose delays/reductions or discontinuations. With the commonly used willingness to pay value of C$50,000/QALY, G-CSF use was not cost-effective compared to ciprofloxacin and deserves scrutiny from the payer perspective.
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spelling pubmed-80950512021-05-13 A multi-centre study comparing granulocyte-colony stimulating factors to antibiotics for primary prophylaxis of docetaxel-cyclophosphamide induced febrile neutropenia Clemons, Mark Fergusson, Dean Joy, Anil A. Thavorn, Kednapa Meza-Junco, Judith Hiller, Julie Price Mackey, John Ng, Terry Zhu, Xiaofu Ibrahim, Mohammed F.K. Sienkiewicz, Marta Saunders, Deanna Vandermeer, Lisa Pond, Gregory Basulaiman, Bassam Awan, Arif Pitre, Lacey Nixon, Nancy A. Hutton, Brian Hilton, John F. Breast Original Article BACKGROUND: Primary febrile neutropenia (FN) prophylaxis with ciprofloxacin or granulocyte-colony stimulating factors (G-CSF) is recommended with docetaxel-cyclophosphamide (TC) chemotherapy for early-stage breast cancer (EBC). A pragmatic randomised trial compared the superiority of G-CSF to ciprofloxacin and a cost-utility analysis were conducted. METHODS: EBC patients receiving TC chemotherapy were randomised to ciprofloxacin or G-CSF. The primary outcome was a composite of FN and non-FN treatment-related hospitalisation. Secondary outcomes included; rates of FN, non-FN treatment-related hospitalisation, chemotherapy dose reductions/delays/discontinuations. Primary analysis was performed with the intention to treat population. Cost-utility analyses were conducted from the Canadian public payer perspective. RESULTS: 458 eligible patients were randomised: 228 to ciprofloxacin and 230 to G-CSF. For the primary endpoint there was non-statistically significant difference (Risk difference = −6.7%, 95%CI = −13.5%–0.1%, p = 0.061) between ciprofloxacin patients (46,20.2%) and G-CSF (31,13.5%). Patients receiving ciprofloxacin were more likely to experience FN (36/228, 15.8% vs 13/230, 5.7%) than patients receiving G-CSF (p < 0.001). Non-FN treatment-related hospitalisation occurred in 40/228 (17.5%) of ciprofloxacin patients vs 28/230 (12.2%) of G-CSF patients (p = 0.12). There were no differences in other secondary outcomes. G-CSF was associated with an incremental cost-effectiveness ratio of C$1,760,796 per one quality-adjusted life year gained. CONCLUSION: The primary endpoint of superiority of G-CSF over ciprofloxacin was not demonstrated. While there were reduced FN rates with G-CSF, there were no differences in chemotherapy dose delays/reductions or discontinuations. With the commonly used willingness to pay value of C$50,000/QALY, G-CSF use was not cost-effective compared to ciprofloxacin and deserves scrutiny from the payer perspective. Elsevier 2021-04-01 /pmc/articles/PMC8095051/ /pubmed/33901921 http://dx.doi.org/10.1016/j.breast.2021.03.012 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Clemons, Mark
Fergusson, Dean
Joy, Anil A.
Thavorn, Kednapa
Meza-Junco, Judith
Hiller, Julie Price
Mackey, John
Ng, Terry
Zhu, Xiaofu
Ibrahim, Mohammed F.K.
Sienkiewicz, Marta
Saunders, Deanna
Vandermeer, Lisa
Pond, Gregory
Basulaiman, Bassam
Awan, Arif
Pitre, Lacey
Nixon, Nancy A.
Hutton, Brian
Hilton, John F.
A multi-centre study comparing granulocyte-colony stimulating factors to antibiotics for primary prophylaxis of docetaxel-cyclophosphamide induced febrile neutropenia
title A multi-centre study comparing granulocyte-colony stimulating factors to antibiotics for primary prophylaxis of docetaxel-cyclophosphamide induced febrile neutropenia
title_full A multi-centre study comparing granulocyte-colony stimulating factors to antibiotics for primary prophylaxis of docetaxel-cyclophosphamide induced febrile neutropenia
title_fullStr A multi-centre study comparing granulocyte-colony stimulating factors to antibiotics for primary prophylaxis of docetaxel-cyclophosphamide induced febrile neutropenia
title_full_unstemmed A multi-centre study comparing granulocyte-colony stimulating factors to antibiotics for primary prophylaxis of docetaxel-cyclophosphamide induced febrile neutropenia
title_short A multi-centre study comparing granulocyte-colony stimulating factors to antibiotics for primary prophylaxis of docetaxel-cyclophosphamide induced febrile neutropenia
title_sort multi-centre study comparing granulocyte-colony stimulating factors to antibiotics for primary prophylaxis of docetaxel-cyclophosphamide induced febrile neutropenia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8095051/
https://www.ncbi.nlm.nih.gov/pubmed/33901921
http://dx.doi.org/10.1016/j.breast.2021.03.012
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