Abstract

BackgroundThe effectiveness of Sacituzumab Govitecan (SG) for metastatic triple-negative breast cancer (mTNBC) has been demonstrated. We aimed to evaluate its cost-effectiveness on mTNBC from the Chinese and United States (US) perspective.MethodsA partitioned survival model was developed to compare the cost and effectiveness of SG versus single-agent chemotherapy based on clinical data from the ASCENT phase 3 randomized trial. Cost and utility data were obtained from the literature. The incremental cost-effectiveness ratio (ICER) was measured, and one-way and probabilistic sensitivity analyses (PSA) were performed to observe model stability. A Markov model was constructed to validate the results.ResultsIn China, SG yielded an additional 0.35 quality-adjusted life-year (QALY) at an additional cost of Chinese Renminbi ¥2257842. The ICER was ¥6375856 ($924037)/QALY. In the US, SG yielded the same additional QALY at an extra cost of $175393 and the ICER was $494479/QALY. Similar results were obtained from the Markov model. One-way sensitivity analyses showed that SG price had the greatest impact on the ICER. PSA showed the probability of SG to be cost-effective when compared with chemotherapy was zero at the current willing-to-pay threshold of ¥217341/QALY and $150000/QALY in China and the US, respectively. The probability of cost-effectiveness of SG would approximate 50% if its price was reduced to ¥10.44/mg in China and $3.65/mg in the US.ConclusionSG is unlikely to be a cost-effective treatment of mTNBC at the current price both in China and the US.

Highlights

  • Breast cancer is the most commonly diagnosed malignant tumor among females and the leading cause of cancer death

  • One-way sensitivity analyses showed that Sacituzumab govitecan (SG) price had the greatest impact on the incremental cost-effectiveness ratio (ICER)

  • probabilistic sensitivity analyses (PSA) showed the probability of SG to be cost-effective when compared with chemotherapy was zero at the current willing-to-pay threshold of ¥217341/quality-adjusted life-year (QALY) and $150000/QALY in China and the United States (US), respectively

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Summary

Introduction

Breast cancer is the most commonly diagnosed malignant tumor among females and the leading cause of cancer death. Intravenous SG received accelerated approval from the Food and Drug Administration (FDA) of the United States (US) on 22 April 2020 for the treatment of mTNBC (7) and the FDA granted regular approval to SG on 7 April 2021 (8). These approvals were based on the results of a phase I/II trial (NCT01631552) (9) and a confirmatory phase III trial (NCT02574455) (10). The effectiveness of Sacituzumab Govitecan (SG) for metastatic triple-negative breast cancer (mTNBC) has been demonstrated. We aimed to evaluate its cost-effectiveness on mTNBC from the Chinese and United States (US) perspective

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