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Cocktail and Poster Display session

83P - Cost-effectiveness analysis of talazoparib maintenance treatment for patients with germline BRCA1/2 mutated HER2-negative advanced breast cancer in China and the US

Date

26 Feb 2024

Session

Cocktail and Poster Display session

Topics

Cancer Care Equity Principles and Health Economics

Tumour Site

Breast Cancer

Presenters

qiaoping xu

Citation

Annals of Oncology (2024) 9 (suppl_1): 1-4. 10.1016/esmoop/esmoop102302

Authors

Q. xu

Author affiliations

  • Clinical Pharmacy Center, Hang zhou first people's hospital, 310000 - Hangzhou/CN

Resources

This content is available to ESMO members and event participants.

Abstract 83P

Background

For breast cancer with BRCA1/2 gene mutation, the PARP inhibitor talazoparib has been proven to have a tumor therapeutic effect and has shown good efficacy in phase III clinical trials. Based on the phase III EMBRACE trial (NCT01945775) clinical trials, we evaluated for the first time the cost-effectiveness of maintenance talazoparib with HER2-negative advanced breast cancer.

Methods

We constructed a Markov model for the economic evaluation of patients who received talazoparib or the physician’s choice of chemotherapy. The state transition probabilities and clinical data were extracted from the phase III EMBRACA clinical trials. The health outcomes are expressed by quality-adjusted life years (QALYs). All costs and incremental cost-effectiveness ratios (ICERs) are presented in US dollars. One-way deterministic sensitivity analysis and probabilistic sensitivity analysis were performed to assess the uncertainty of the models. The unit prices of medicines were obtained from the West China Hospital, Red Book, and published literature. Outcomes were measured in quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratio, which robustness was evaluated by deterministic and probabilistic sensitivity analyses.

Results

Based on the Chinese Markov model, the base case ICER for talazoparib versus the control group, with incremental costs of $2484.48/QALY and an incremental QALY of 1.5, indicating that it was cost-effective from the aspect of the Chinese healthcare system. However, as shown by the American Markov model,talazoparib was dominant versus the control group, with a cost saving of $10223.43 and a gain of 1.5 QALYs.One-way deterministic sensitivity analyses showed that the economic benefits generated by the use of talazoparib as a treatment strategy in both China and the US are much greater.

Conclusions

Talazoparib was estimated to be more cost-effective than the maintenance therapy of patients with germline BRCA1/2 mutated HER2-negative advanced breast cancer in China and the US at thresholds of $3185/month and $19100/month per QALY, respectively.

Clinical trial identification

[2014] Scientific Research Medical Ethics No. (028)-01.

Editorial acknowledgement

Legal entity responsible for the study

The author.

Funding

Key Medical Discipline of Hangzhou City.

Disclosure

The author has declared no conflicts of interest.

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