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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).
Waks, Adrienne G; Chen, Emily L; Graham, Noah; Frey, Anna Mae; Almeida, Kenneth; Attaya, Victoria; Ryding, Cari; Abbass, Ibrahim; Fung, Anita; Sussell, Jesse; Cortazar, Patricia; Harvey, Caroline; Leth, Denise; Faggen, Meredith; Sinclair, Natalie; Walsh, Jeanna; Tung, Nadine; Sinclair, Sarah; Lo, Steve; Yardley, Denise; Valero, Vicente; Meisel, Jane; Ballinger, Tarah J; Adams, Sylvia; Carey, Lisa A; Rauch, Julia K; Abramson, Vandana G; Williams, Nicole O; Chen, Wendy Y; Leone, Jose P; Schumer, Susan T; Tayob, Nabihah; Tolaney, Sara M.
Affiliation
  • Waks AG; Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Chen EL; Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.
  • Graham N; Harvard Medical School, Boston, MA.
  • Frey AM; Brigham and Women's Hospital, Boston, MA.
  • Almeida K; Data Sciences, Dana-Farber Cancer Institute, Boston, MA.
  • Attaya V; Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Ryding C; Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.
  • Abbass I; Harvard Medical School, Boston, MA.
  • Fung A; Pharmacy and Clinical Support, Dana-Farber Cancer Institute, Boston, MA.
  • Sussell J; Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Cortazar P; Current Affiliation: Olema Oncology, San Francisco, CA.
  • Harvey C; Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Leth D; Genentech, Inc, South San Francisco, CA.
  • Faggen M; Genentech, Inc, South San Francisco, CA.
  • Sinclair N; Genentech, Inc, South San Francisco, CA.
  • Walsh J; Genentech, Inc, South San Francisco, CA.
  • Tung N; Pharmacy and Clinical Support, Dana-Farber Cancer Institute, Boston, MA.
  • Sinclair S; Pharmacy and Clinical Support, Dana-Farber Cancer Institute, Boston, MA.
  • Lo S; Dana-Farber Brigham Cancer Center in Clinical Affiliation With South Shore Hospital, Weymouth, MA.
  • Yardley D; Dana-Farber Brigham Cancer Center-Foxborough and Milford, Foxborough, MA.
  • Valero V; Dana-Farber/New Hampshire Oncology-Hematology, Londonderry, NH.
  • Meisel J; Harvard Medical School, Boston, MA.
  • Ballinger TJ; Beth Israel Deaconess Medical Center, Boston, MA.
  • Adams S; Eastern Maine Medical Center, Brewer, ME.
  • Carey LA; Bennett Cancer Center, Stamford Health, Stamford, CT.
  • Rauch JK; Sarah Cannon Research Institute, Nashville, TN.
  • Abramson VG; The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Williams NO; Winship Cancer Institute at Emory University, Atlanta, GA.
  • Chen WY; Indiana University School of Medicine, Indianapolis, IN.
  • Leone JP; Perlmutter Cancer Center, NYU Langone Health, New York, NY.
  • Schumer ST; Department of Medicine, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Tayob N; UNC Health, Garner, NC.
  • Tolaney SM; Vanderbilt University Medical Center, Nashville, TN.
JCO Oncol Pract ; : OP2400021, 2024 Jul 19.
Article in En | MEDLINE | ID: mdl-39028923
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 v 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 v 84.3 minutes; P < .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 v 177.8 minutes; P < .0001). The pharmacy workflow time was 78.2 minutes shorter for SC versus IV formulation (41 v 119.2 minutes; P < .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.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JCO Oncol Pract / JCO oncology practice (Online) Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JCO Oncol Pract / JCO oncology practice (Online) Year: 2024 Document type: Article Country of publication: