Subcutaneous vs Intravenous Trastuzumab/Pertuzumab: A Time and Motion Substudy of a Phase II Trial of Adjuvant Trastuzumab/Pertuzumab for Stage I HER2+ Breast Cancer (ADEPT trial).

PURPOSE: The time required for in-clinic drug administration can substantially affect breast cancer patients' quality of life. Subcutaneous (SC) drug administration, as opposed to intravenous (IV), may reduce this time commitment. This study sought to estimate the difference in time burden between IV and SC administration of trastuzumab and pertuzumab (HP). METHODS: We prospectively enrolled a subcohort of patients participating in the ADEPT trial (ClinicalTrials.gov identifier: NCT04569747, investigating adjuvant HP plus endocrine therapy for stage I human epidermal growth factor receptor 2-positive breast cancer) to this single-arm crossover time and motion substudy. Patients received two cycles of IV HP followed by two cycles of SC HP. During each cycle, time points in drug preparation and administration were captured. The primary end point was total patient time in the treatment chair. Additional end points included total patient treatment experience time and total pharmacy workflow time. A sample size of 22 patients was estimated to provide 90.7% power with two-sided alpha .05 to detect a difference of 70 minutes in the primary end point by treatment arm (IV <i>v</i> SC). RESULTS: Twenty-two patients were enrolled. The mean total patient time in the treatment chair was 61.8 minutes shorter with SC versus IV HP (22.5 <i>v</i> 84.3 minutes; <i>P</i> &lt; .0001). The mean total patient treatment experience time (incorporating time spent waiting for treatment initiation and time spent in the treatment chair) was 81.8 minutes shorter for SC administration (96 <i>v</i> 177.8 minutes; <i>P</i> &lt; .0001). The pharmacy workflow time was 78.2 minutes shorter for SC versus IV formulation (41 <i>v</i> 119.2 minutes; <i>P</i> &lt; .0001). CONCLUSION: SC administration of HP shortened patient time burden by approximately 1 hour. SC drug administration can facilitate faster workflows for health care professionals and improve patients' breast cancer treatment experience.

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UNC Libraries
Published
2024-10-09
DOI
https://doi.org/10.17615/6k1s-ym34
Primary Topic
HER2/EGFR in Cancer Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Subcutaneous vs Intravenous Trastuzumab/Pertuzumab: A Time and Motion Substudy of a Phase II Trial of Adjuvant Trastuzumab/Pertuzumab for Stage I HER2+ Breast Cancer (ADEPT trial).

Anna Frey, Caroline Harvey, Julia K. Rauch, Susan Schumer et al.
UNC Libraries
HER2/EGFR in Cancer Research
article

Subcutaneous vs Intravenous Trastuzumab/Pertuzumab: A Time and Motion Substudy of a Phase II Trial of Adjuvant Trastuzumab/Pertuzumab for Stage I HER2+ Breast Cancer (ADEPT trial).

Anna Frey, Caroline Harvey, Julia K. Rauch, Susan Schumer, Natalie Sinclair, Denise A. Yardley, Jesse Sussell, Sylvia Adams, Nicole Williams, Ibrahim M. Abbass, Lisa A. Carey, José Pablo Leone, Anita Fung, Nadine Tung, Nabihah Tayob, Steve Lo, Tarah J. Ballinger, Sara M. Tolaney, Vandana G. Abramson, Patricia Cortazar, Vicente Valero, Jane Meisel, Victoria Attaya, Adrienne Gropper Waks, Noah Graham, Denise Leth, Emily Chen, Sarah Sinclair, Jeanna Walsh, Meredith Faggen, Kenneth Almeida, Cari Ryding, Wendy Y. Chen
article en

Abstract

PURPOSE: The time required for in-clinic drug administration can substantially affect breast cancer patients' quality of life. Subcutaneous (SC) drug administration, as opposed to intravenous (IV), may reduce this time commitment. This study sought to estimate the difference in time burden between IV and SC administration of trastuzumab and pertuzumab (HP). METHODS: We prospectively enrolled a subcohort of patients participating in the ADEPT trial (ClinicalTrials.gov identifier: NCT04569747, investigating adjuvant HP plus endocrine therapy for stage I human epidermal growth factor receptor 2-positive breast cancer) to this single-arm crossover time and motion substudy. Patients received two cycles of IV HP followed by two cycles of SC HP. During each cycle, time points in drug preparation and administration were captured. The primary end point was total patient time in the treatment chair. Additional end points included total patient treatment experience time and total pharmacy workflow time. A sample size of 22 patients was estimated to provide 90.7% power with two-sided alpha .05 to detect a difference of 70 minutes in the primary end point by treatment arm (IV <i>v</i> SC). RESULTS: Twenty-two patients were enrolled. The mean total patient time in the treatment chair was 61.8 minutes shorter with SC versus IV HP (22.5 <i>v</i> 84.3 minutes; <i>P</i> &lt; .0001). The mean total patient treatment experience time (incorporating time spent waiting for treatment initiation and time spent in the treatment chair) was 81.8 minutes shorter for SC administration (96 <i>v</i> 177.8 minutes; <i>P</i> &lt; .0001). The pharmacy workflow time was 78.2 minutes shorter for SC versus IV formulation (41 <i>v</i> 119.2 minutes; <i>P</i> &lt; .0001). CONCLUSION: SC administration of HP shortened patient time burden by approximately 1 hour. SC drug administration can facilitate faster workflows for health care professionals and improve patients' breast cancer treatment experience.

UNC Libraries
University of North Carolina at Chapel Hill (US)
Amgen, Eli Lilly and Company, Pfizer, AstraZeneca, GlaxoSmithKline, Gilead Sciences, National Comprehensive Cancer Network, bluebird bio, Incyte, Moderna, MacroGenics, G1 Therapeutics, Eisai, Genentech, Daiichi Sankyo Europe
Good health and well-being
Openalex Percentile: Top 69%
HER2/EGFR in Cancer Research
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