» Articles » PMID: 26251623

Medical Resource Utilization for Administration of Trastuzumab in a New Zealand Oncology Outpatient Setting: a Time and Motion Study

Overview
Publisher Dove Medical Press
Specialty Health Services
Date 2015 Aug 8
PMID 26251623
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Background: In New Zealand, trastuzumab is standard therapy for human epidermal growth factor receptor-2 (HER2)-positive early and metastatic breast cancer. Given the requirement for ongoing adjuvant or maintenance treatment and intravenous (IV) delivery, such a regimen consumes considerable health care resources. The development of a subcutaneous (SC) trastuzumab formulation with a short administration time offers the potential to reduce hospital expenditure. The aim of this study was to determine medical resource utilization associated with administration of trastuzumab SC injection via handheld syringe vs trastuzumab IV infusion in patients with HER2-positive breast cancer in New Zealand.

Methods: This noninterventional, descriptive study was conducted at the outpatient oncology centers at Auckland City and Tauranga Hospitals. Trained observers recorded times associated with health care professional (HCP) tasks and consumables use associated with preparation and administration of trastuzumab IV or SC in women with early or metastatic breast cancer. The cost for each formulation was calculated as the mean cost of HCP time (based on Pharmaceutical Management Agency hourly rates) plus the mean cost of consumables used.

Results: Use of trastuzumab SC vs IV reduced mean chair time by 36.95 minutes and total nurse time by 6.12 minutes; there was a 20.45-minute reduction in pharmacist time when the SC formulation was used. After adding consumable costs, the overall estimated saving with trastuzumab SC vs IV was $76.94 (New Zealand dollars) per patient per cycle.

Conclusions: Compared with trastuzumab IV infusion, administration of trastuzumab via SC injection reduced time spent in the clinic and decreased HCP resources and consumables needed to administer treatment. These reductions could contribute to a decrease in health care costs and an improvement in the efficiency of HER2-positive breast cancer treatment delivery.

Citing Articles

The burden of systemic therapy administration route in treating HER2-positive breast cancer (for patients, healthcare professionals, and healthcare system): a systematic literature review.

Landeiro L, Martins T, Grigolon R, Monteiro I, Balardin J, Padilha E Front Pharmacol. 2024; 15:1338546.

PMID: 39224777 PMC: 11366779. DOI: 10.3389/fphar.2024.1338546.


Subcutaneous versus intravenous administration of Trastuzumab: a minimization cost analysis with real world data from a reference cancer centre in Peru.

Otoya I, Valdiviezo N, Roque K, Morante Z, Vidaurre T, Neciosup S Ecancermedicalscience. 2024; 18:1708.

PMID: 39021543 PMC: 11254399. DOI: 10.3332/ecancer.2024.1708.


ENTIMOS: Decision Support Tool Highlights Potential Impact of Non-intravenous Therapies for Multiple Sclerosis on Patient Care via Clinical Scenario Simulation.

Nicholas R, Scalfaro E, Dorsey R, Angehrn Z, Banhazi J, Brennan R Pharmacoecon Open. 2024; 8(5):755-764.

PMID: 38990487 PMC: 11362419. DOI: 10.1007/s41669-024-00493-8.


Practice efficiency and total cost of care with bispecifics and CAR-T in relapsed/refractory diffuse large B-cell lymphoma: an institutional perspective.

Lei M, Li Q, ODay K, Meyer K, Wang A, Jun M Future Oncol. 2024; 20(29):2189-2201.

PMID: 38913826 PMC: 11508956. DOI: 10.1080/14796694.2024.2354157.


Cost minimization analysis of subcutaneous trastuzumab versus intravenous biosimilar trastuzumab: policy recommendations for breast cancer treatment in Malaysia.

Heng J, Raman S, Wong Z, Beh V Daru. 2023; 32(1):67-76.

PMID: 37903943 PMC: 11087381. DOI: 10.1007/s40199-023-00485-9.


References
1.
Rosenthal V, Guzman S, Migone O, Crnich C . The attributable cost, length of hospital stay, and mortality of central line-associated bloodstream infection in intensive care departments in Argentina: A prospective, matched analysis. Am J Infect Control. 2003; 31(8):475-80. DOI: 10.1016/j.ajic.2003.03.002. View

2.
Ismael G, Hegg R, Muehlbauer S, Heinzmann D, Lum B, Kim S . 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. Lancet Oncol. 2012; 13(9):869-78. DOI: 10.1016/S1470-2045(12)70329-7. View

3.
Wynne C, Harvey V, Schwabe C, Waaka D, McIntyre C, Bittner B . Comparison of subcutaneous and intravenous administration of trastuzumab: a phase I/Ib trial in healthy male volunteers and patients with HER2-positive breast cancer. J Clin Pharmacol. 2013; 53(2):192-201. DOI: 10.1177/0091270012436560. View

4.
Bookbinder L, Hofer A, Haller M, Zepeda M, Keller G, Lim J . A recombinant human enzyme for enhanced interstitial transport of therapeutics. J Control Release. 2006; 114(2):230-41. DOI: 10.1016/j.jconrel.2006.05.027. View

5.
Launay-Vacher V . An appraisal of subcutaneous trastuzumab: a new formulation meeting clinical needs. Cancer Chemother Pharmacol. 2013; 72(6):1361-7. DOI: 10.1007/s00280-013-2289-4. View