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A time and motion study of subcutaneous versus intravenous trastuzumab in patients with HER2‐positive early breast cancer
Within PrefHer (NCT01401166), patients and healthcare professionals (HCPs) preferred subcutaneous (SC) over intravenous (IV) trastuzumab. We undertook a prospective, observational time and motion study to quantify patients’ time in infusion chairs and active HCP time in PrefHer. Patients with HER2‐p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799946/ https://www.ncbi.nlm.nih.gov/pubmed/26806010 http://dx.doi.org/10.1002/cam4.573 |
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author | De Cock, Erwin Pivot, Xavier Hauser, Nik Verma, Sunil Kritikou, Persefoni Millar, Douglas Knoop, Ann |
author_facet | De Cock, Erwin Pivot, Xavier Hauser, Nik Verma, Sunil Kritikou, Persefoni Millar, Douglas Knoop, Ann |
author_sort | De Cock, Erwin |
collection | PubMed |
description | Within PrefHer (NCT01401166), patients and healthcare professionals (HCPs) preferred subcutaneous (SC) over intravenous (IV) trastuzumab. We undertook a prospective, observational time and motion study to quantify patients’ time in infusion chairs and active HCP time in PrefHer. Patients with HER2‐positive early breast cancer received four adjuvant cycles of SC trastuzumab (600 mg fixed dose via SC single‐use injection device [SID, Cohort 1] or SC handheld syringe [HHS, Cohort 2]) then four cycles of standard IV trastuzumab or the reverse sequence. Generic case report forms for IV and SC management, both in the treatment room and the drug preparation area, were tailored to reflect center practices. Patient chair time and active HCP time were recorded. We compared pooled Cohort 1 + 2 IV with Cohort 1 SC SID and Cohort 2 SC HHS mean times across eight countries and individually within them utilizing a random intercept generalized linear mixed‐effects model. Per session, the SC SID saved a mean of 57 min of patient chair time versus IV (range across countries: 47–86; P < 0.0001); the SC HHS saved 55 min (40–81; P < 0.0001). Active HCP time was reduced by a mean of 13 min per session with the SC SID (range across countries: 4–16; P < 0.0001) and 17 min with the SC HHS (5–28; P < 0.0001) versus IV. SC trastuzumab, delivered via SID or HHS, saved patient chair and active HCP times versus IV infusion, supporting a transition to either SC method. |
format | Online Article Text |
id | pubmed-4799946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47999462016-04-08 A time and motion study of subcutaneous versus intravenous trastuzumab in patients with HER2‐positive early breast cancer De Cock, Erwin Pivot, Xavier Hauser, Nik Verma, Sunil Kritikou, Persefoni Millar, Douglas Knoop, Ann Cancer Med Clinical Cancer Research Within PrefHer (NCT01401166), patients and healthcare professionals (HCPs) preferred subcutaneous (SC) over intravenous (IV) trastuzumab. We undertook a prospective, observational time and motion study to quantify patients’ time in infusion chairs and active HCP time in PrefHer. Patients with HER2‐positive early breast cancer received four adjuvant cycles of SC trastuzumab (600 mg fixed dose via SC single‐use injection device [SID, Cohort 1] or SC handheld syringe [HHS, Cohort 2]) then four cycles of standard IV trastuzumab or the reverse sequence. Generic case report forms for IV and SC management, both in the treatment room and the drug preparation area, were tailored to reflect center practices. Patient chair time and active HCP time were recorded. We compared pooled Cohort 1 + 2 IV with Cohort 1 SC SID and Cohort 2 SC HHS mean times across eight countries and individually within them utilizing a random intercept generalized linear mixed‐effects model. Per session, the SC SID saved a mean of 57 min of patient chair time versus IV (range across countries: 47–86; P < 0.0001); the SC HHS saved 55 min (40–81; P < 0.0001). Active HCP time was reduced by a mean of 13 min per session with the SC SID (range across countries: 4–16; P < 0.0001) and 17 min with the SC HHS (5–28; P < 0.0001) versus IV. SC trastuzumab, delivered via SID or HHS, saved patient chair and active HCP times versus IV infusion, supporting a transition to either SC method. John Wiley and Sons Inc. 2016-01-25 /pmc/articles/PMC4799946/ /pubmed/26806010 http://dx.doi.org/10.1002/cam4.573 Text en © 2016 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research De Cock, Erwin Pivot, Xavier Hauser, Nik Verma, Sunil Kritikou, Persefoni Millar, Douglas Knoop, Ann A time and motion study of subcutaneous versus intravenous trastuzumab in patients with HER2‐positive early breast cancer |
title | A time and motion study of subcutaneous versus intravenous trastuzumab in patients with HER2‐positive early breast cancer |
title_full | A time and motion study of subcutaneous versus intravenous trastuzumab in patients with HER2‐positive early breast cancer |
title_fullStr | A time and motion study of subcutaneous versus intravenous trastuzumab in patients with HER2‐positive early breast cancer |
title_full_unstemmed | A time and motion study of subcutaneous versus intravenous trastuzumab in patients with HER2‐positive early breast cancer |
title_short | A time and motion study of subcutaneous versus intravenous trastuzumab in patients with HER2‐positive early breast cancer |
title_sort | time and motion study of subcutaneous versus intravenous trastuzumab in patients with her2‐positive early breast cancer |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799946/ https://www.ncbi.nlm.nih.gov/pubmed/26806010 http://dx.doi.org/10.1002/cam4.573 |
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