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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...

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Autores principales: De Cock, Erwin, Pivot, Xavier, Hauser, Nik, Verma, Sunil, Kritikou, Persefoni, Millar, Douglas, Knoop, Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
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.
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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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