Immune checkpoint inhibitors plus chemotherapy for HER2-negative advanced gastric/gastroesophageal junction cancer: a cost-effectiveness analysis

Author:

Zhu Youwen1,Liu Kun1,Zhu Hong12ORCID,Wu Haijun34

Affiliation:

1. Department of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China

2. National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China

3. Department of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China

4. National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China

Abstract

Background: Nivolumab plus chemotherapy (NC) was recently approved as the first-line intervention for human epidermal growth factor receptor 2-negative advanced gastric/gastroesophageal junction cancer (GC/GEJC). Moreover, in the latest KEYNOTE-859 (NCT03675737), pembrolizumab plus chemotherapy (PC) was demonstrated to produce remarkable patient survival outcomes. Objectives: The clinicians and patients need to assess NC and PC preference for cancer drugs. Design: The cost-effective analysis. Methods: In an economic assessment of the United States, United Kingdom, and Chinese healthcare systems using a Markov model simulated patients with GC/GEJC, two treatment decision branches with three health states and a tracked time horizon of 15 years were developed. The overall cost and efficacy outcomes of first-line strategies PC and NC were evaluated at willingness-to-pay (WTP) thresholds of different national, including life-years (LYs), quality-adjusted life-years (QALYs), incremental cost-effectiveness ratios (ICERs), and incremental net-health benefit (INHB). Sensitivity and subgroup analyses were considered. Results: Given a WTP threshold of $150,000, $60,161, and $37,653 per QALY in the United States, United Kingdom, and China, respectively, both PC and NC achieved QALYs of 1.67 and 1.65 (2.51 and 2.48 LYs), 1.65 and 1.63 (2.48 and 2.45 LYs), and 1.60 and 1.58 (2.40 and 2.37 LYs), with total costs of $242,444 and $232,617, $148,367 and $127,737, and $16,693 and $24,016, respectively. Based on our sensitivity analysis, the programmed death-1 inhibitors cost produced the largest impact on the outcome. In addition, the cost-effectiveness probabilities of PC were 38.3%, 4.1%, and 100% in the three aforementioned countries, respectively. Conclusion: In the case of the Chinese payers’ perspective, PC appeared more dominant as first-line therapy for advanced GC/GEJC patients, whereas NC was preferred in the United States and United Kingdom.

Funder

The Natural Science Foundation of Hunan Province

Publisher

SAGE Publications

Subject

Gastroenterology

Reference46 articles.

1. World Health Organization. Gastric cancer, https://gco.iarc.fr/today/data/factsheets/cancers/7-Stomach-fact-sheet.pdf (2020, accessed December 2020).

2. Comparative efficacy and tolerability of targeted and immunotherapy combined with chemotherapy as first-line treatment for advanced gastric cancer: a Bayesian network meta-analysis

3. American Cancer Society. Gastric cancer, https://www.cancer.org/content/dam/CRC/PDF/Public/8838.00.pdf (2021, accessed January 2021).

4. The KEYNOTE-811 trial of dual PD-1 and HER2 blockade in HER2-positive gastric cancer

5. US Food and Drug Administration. FDA Approves first immunotherapy for initial treatment of gastric cancer, https://www.fda.gov/news-events/press-announcements/fda-approves-first-immunotherapy-initial-treatment-gastric-cancer (2021, accessed April 2021).

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