Cost-utility analysis of trastuzumab deruxtecan versus trastuzumab emtansine in HER2-positive metastatic breast cancer in Chinese setting

J Cancer Res Clin Oncol. 2023 Dec;149(20):17933-17942. doi: 10.1007/s00432-023-05496-2. Epub 2023 Nov 14.

Abstract

Purpose: Trastuzumab deruxtecan (T-DXd) expressed substantial improvement in the progression-free survival and overall survival contrasted with trastuzumab emtansine (T-DM1) in patients with HER2-positive metastatic breast cancer (mBC), becoming the second-line standard of care, promisingly. We aim to estimate the cost-utility of T-DXd versus T-DM1 in HER2-positive mBC from the Chinese healthcare perspective.

Methods: A partitioned survival model was applied to examine the cost-utility of T-DXd versus T-DM1. Clinical patients and outcome data were sourced from the DESTINY-Breast 03 trial. Costs and utilities were sourced in Chinese setting. Total costs, quality-adjusted life months (QALMs), and an incremental cost-utility ratios (ICUR) were calculated for cost-utility analysis. The willingness-to-pay threshold was set at $3188/QALM. Univariate, scenario, and probabilistic sensitivity analyses were performed.

Results: T-DXd group gained ∆QALM of 7.09 months and ∆Cost of $304,503 compared with T-DM1 therapy, which caused an ICUR of $42,936/QALM. The results of sensitivity analyses confirmed the base-case findings. Furthermore, T-DXd must reduce the price to enter the Chinese mainland market. At least when the cycle cost of T-DXd is reduced to $2975, T-DXd has an 83.3% chance of becoming a better choice.

Conclusions: T-DXd appears to be not cost effective compared with T-DM1 for HER2-positive mBC patients previously treated with trastuzumab and a taxane.

Keywords: Cost–utility analysis; HER2-positive metastatic breast; Price exploring; Trastuzumab deruxtecan; Trastuzumab emtansine.

MeSH terms

  • Ado-Trastuzumab Emtansine / therapeutic use
  • Breast Neoplasms* / pathology
  • China
  • Cost-Benefit Analysis
  • Female
  • Humans
  • Maytansine* / therapeutic use
  • Receptor, ErbB-2
  • Trastuzumab / therapeutic use

Substances

  • trastuzumab deruxtecan
  • Ado-Trastuzumab Emtansine
  • Receptor, ErbB-2
  • Maytansine
  • Trastuzumab