A newly published study finds that subcutaneous administration of trastuzumab produces substantial time savings for healthcare providers and patients, as well as reduced costs.
In patients with early or metastatic HER2-positive breast cancer or HER2-positive metastatic gastric cancer, trastuzumab is administered every 3 weeks for 1 year (or until disease progression) by intravenous infusion. The duration of administration is typically 90 minutes in the first infusion, and 30 minutes for each subsequent administration. A subcutaneous (SC) administration of reference trastuzumab, Herceptin, is approved for use in the European Union (and is undergoing a phase 3 trial in the United States). A newly published study, appearing in Clinical and Translational Oncology, finds that SC administration of trastuzumab produces substantial time savings for healthcare providers and patients, as well as reduced costs.
The prospective, observational time-and-motion study conducted in 3 medical centers in Spain recorded the active time that providers expended on trastuzumab SC- and intravenous- (IV) related tasks (including collection, reconstitution, and signing off on the prepared trastuzumab, as well as installing the venous catheter, administering pre-medications, monitoring the patient, and other tasks), and calculated provider time as the mean sum of tasks over 154 administrations. Researchers also calculated mean patient infusion chair time and treatment room time.
Staff costs were calculated using Spanish salaries, and direct costs (including the cost of consumables and of trastuzumab) and indirect costs (including loss of productivity) were also calculated.
In total, 159 patients received trastuzumab in IV administration, and 148 patients received SC trastuzumab. SC administration was associated with reduced active provider time in all 3 centers, with an average time of 13.2 minutes (95% CI; range, 8.9-17.5) versus 27.2 minutes for IV administration (95% CI; range, 2.18-32.6). The greatest reduction was in nursing time, but there were also significant reductions in pharmacist and nursing assistant time.
SC administration also reduced the time spent in the treatment room, as it eliminated catheter, premedication, drug transport, and monitoring tasks. In the preparation area, SC trastuzumab resulted in reduced material preparation time (3.9 minutes versus 6.0 minutes) and drug reconstitution time (0 minutes versus 5.9 minutes). The researchers estimate that a complete treatment cycle of IV trastuzumab would require 8.2 hours of provider time, while a complete treatment cycle of SC trastuzumab would require 4 hours.
SC trastuzumab for 18 cycles for 1 patient was estimated to save €121.57 ($143.39) in provider time costs, €112.52 ($132.72) in consumables, and €745.51 ($879.31) in the cost of trastuzumab (measured by reported ex-factory price). In terms of indirect costs (lost productivity), SC trastuzumab reduced per-patient costs for an 18-cycle treatment by €152.83 ($180.26). SC trastuzumab provided an overall cost savings (including direct and indirect costs) of €1132.43 ($1335.68).
The researchers concluded that SC trastuzumab could reduce provider and patient time, and could thereby improve patients’ quality of life and produce cost savings for the Spanish health system. The researchers estimate that 4000 to 5000 women in Spain could be eligible for treatment with trastuzumab for early breast cancer, and the savings realized through SC administration could total as much as €4 million ($4.72 million).
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
Will the FTC Be More PBM-Friendly Under a Second Trump Administration?
February 23rd 2025On this episode of Not So Different, we explore the Federal Trade Commission’s (FTC) second interim report on pharmacy benefit managers (PBMs) with Joe Wisniewski from Turquoise Health, discussing key issues like preferential reimbursement, drug pricing transparency, biosimilars, shifting regulations, and how a second Trump administration could reshape PBM practices.
Targeted Reimbursement Encourages Oncology Biosimilar Use
May 7th 2025Incentivizing physicians with modest financial bonuses may seem like a small step, but in Japan’s outpatient oncology setting, it helped push trastuzumab biosimilars toward broader adoption, demonstrating how even limited reimbursement reforms can reshape prescribing behavior under the right conditions.
Samsung Bioepis Report Signals Turning Point for US Biosimilars
May 1st 2025A wave of biosimilar approvals, aggressive pricing strategies, and a regulatory sea change are setting the stage for unprecedented momentum in the US biologics market, with 2025 already proving to be a landmark year in reshaping cost, access, and innovation across therapeutic areas.