Cost-Utility Analysis of Adjuvant Olaparib for Germline BRCA1/2-Mutated, High-Risk HER2-Negative Early Breast Cancer

Sergio Cedillo1, Almudena González-Domínguez2, Yoana Ivanova-Markova3

  • 1AstraZeneca Farmacéutica Spain S.A., Puerto de Somport 21-23, 28050, Madrid, Spain.

Pharmacoeconomics - Open
|August 19, 2024
PubMed
Abstract

Insights

Olaparib is a cost-effective adjuvant treatment for early HER2-negative breast cancer (BC) with BRCA1/2 gene mutations in Spain. This targeted therapy improves quality-adjusted life years (QALYs) for both hormone receptor-positive and triple-negative patients.

Area of Science:

  • Oncology
  • Health Economics
  • Pharmacoeconomics

Background:

  • Adjuvant olaparib is considered for early HER2-negative breast cancer (BC) with germline BRCA mutations (gBRCAm) and high recurrence risk.
  • The cost-effectiveness of olaparib within the Spanish National Health Service (SNHS) requires evaluation for this patient population.

Purpose of the Study:

  • To estimate the cost-effectiveness of olaparib versus standard of care (SoC) as adjuvant treatment for early gBRCAm HER2-negative BC in the SNHS.
  • To assess the economic value of olaparib for high-risk early-stage breast cancer patients with specific genetic mutations.

Main Methods:

  • A semi-Markov model was adapted for the Spanish healthcare setting with a lifetime horizon.
  • Clinical data from the OlympiA trial and direct healthcare costs were incorporated.
  • Probabilistic sensitivity analysis (PSA) was performed to evaluate cost-effectiveness.

Main Results:

  • Olaparib demonstrated an incremental cost of €44,273-€50,164, with an improvement of 1.14-1.28 quality-adjusted life years (QALYs) for HR+ and TN patients, respectively.
  • The incremental cost-effectiveness ratio (ICER) for olaparib was €38,839/QALY (HR+) and €39,084/QALY (TN).
  • PSA indicated that 75.7% (HR+) and 82.2% (TN) of simulations were below the €60,000/QALY threshold.

Conclusions:

  • Adjuvant olaparib is likely cost-effective for treating early gBRCAm HER2-negative BC in Spain.
  • The findings support the use of olaparib in this specific patient subgroup within the SNHS.