Published June 5, 2019 | Version v1
Journal article Open

Cost-effectiveness of adjuvant paclitaxel and trastuzumab for early-stage node-negative, HER2-positive breast cancer

  • 1. Istanbul Şehir University
  • 2. University of Wisconsin-Madison
  • 3. University of Chicago

Description

Objectives: Adjuvant paclitaxel and trastuzumab has been shown to be an effective regimen with low risk of cancer recurrence and treatment-related toxicities in early-stage node-negative, HER2-positive breast cancer. We investigated the cost-effectiveness of this regimen.

Methods: A Markov-based microsimulation model with six health states is used to simulate four adjuvant therapy options for women with early-stage node-negative, HER2-positive breast cancer at different age groups. The four treatment arms are 1) adjuvant paclitaxel and trastuzumab (TH), 2) doxorubicin, cyclophosphamide, paclitaxel and trastuzumab (ACTH), 3) docetaxel, carboplatin and trastuzumab (TCH), and 4) no adjuvant trastuzumab (NT). Data from randomized trials were used to estimate treatment efficacy. Societal perspective was used in this cost-effectiveness analysis. Costs were measured in 2016 US dollars (US$) and quality-adjusted life-years (QALYs) was used for health outcomes. Sensitivity analyses were performed to evaluate the impact of uncertainty in parameter estimation.

Results: We found that 40-year-old women undergoing TH treatment would have an average of 16.17 QALYs for the cost of 178,650 dollars when lifetime horizon is used. Compared to NT, TH has incremental cost-effectiveness ratios ranged from 10,584 dollars (ages 40–49) to 84,981 dollars (age 80+) per additional QALYs. The sensitivity analysis showed that TH is cheaper and leads to higher QALYs compared to both ACTH and TCH for all age groups and time horizons.

Conclusions: TH is cost-effective for all age groups in the base case scenario and in the sensitivity analysis. In order to reduce the parameter uncertainty, clinical trials with longer follow-up times are needed.

Data availability

All relevant data are within the manuscript and its Supporting Information files.

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Additional details

Identifiers

DOI
10.1371/journal.pone.0217778
Other
oai:uchicago.tind.io:6290

Funding

National Center for Research Resources
Clinical and Translational Science Award

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Medicine