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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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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. |
format | Online Article Text |
id | pubmed-8095051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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