A time and motion study of subcutaneous versus intravenous trastuzumab in patients with HER2-positive early breast cancer

Author:

De Cock Erwin1,Pivot Xavier2,Hauser Nik3,Verma Sunil4,Kritikou Persefoni5,Millar Douglas6,Knoop Ann7

Affiliation:

1. United BioSource Corporation; Barcelona Spain

2. CHU Jean Minjoz; Besançon France

3. Department of Gynecology and Obstetrics; Kantonsspital Baden AG; Baden Switzerland

4. Sunnybrook Odette Cancer Centre; Toronto Ontario Canada

5. United BioSource Corporation; Hammersmith United Kingdom

6. F. Hoffmann-La Roche Ltd; Basel Switzerland

7. Copenhagen University Hospital; Copenhagen Denmark

Funder

F. Hoffmann-La Roche Ltd, Basel, Switzerland

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

Reference10 articles.

1. Ferlay , J. I. Soerjomataram M. Ervik GLOBOCAN 2012 v1.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11 http://globocan.iarc.fr

2. National Comprehensive Cancer Network 2016 NCCN Clinical Practice Guidelines in Oncology: Breast Cancer http://www.nccn.org/professionals/physician_gls/pdf/breast.pdf

3. Primary breast cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up;Senkus;Ann. Oncol.,2015

4. Tailoring therapies-improving the management of early breast cancer: St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2015;Coates;Ann. Oncol.,2015

5. Subcutaneous versus intravenous administration of (neo)adjuvant trastuzumab in patients with HER2-positive, clinical stage I-III breast cancer (HannaH study): a phase 3, open-label, multicentre, randomised trial;Ismael;Lancet Oncol.,2012

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