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Economic Evaluation of First-Line Camrelizumab for Advanced Non-small-cell Lung Cancer in China

Background: As the first domestic PD-1 antibody approved for lung cancer in China, camrelizumab has exhibited proven effectiveness for non-small-cell lung cancer (NSCLC) patients. However, the cost-effectiveness of this new regimen remains to be investigated. Objective: To evaluate the cost-effectiv...

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Autores principales: Xiang, Guiyuan, Gu, Lingna, Chen, Xuan, Wang, Fan, Chen, Bohua, Zhao, Jie, Lu, Yun, Chang, Feng, Zhu, Yumei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702426/
https://www.ncbi.nlm.nih.gov/pubmed/34957008
http://dx.doi.org/10.3389/fpubh.2021.743558
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author Xiang, Guiyuan
Gu, Lingna
Chen, Xuan
Wang, Fan
Chen, Bohua
Zhao, Jie
Lu, Yun
Chang, Feng
Zhu, Yumei
author_facet Xiang, Guiyuan
Gu, Lingna
Chen, Xuan
Wang, Fan
Chen, Bohua
Zhao, Jie
Lu, Yun
Chang, Feng
Zhu, Yumei
author_sort Xiang, Guiyuan
collection PubMed
description Background: As the first domestic PD-1 antibody approved for lung cancer in China, camrelizumab has exhibited proven effectiveness for non-small-cell lung cancer (NSCLC) patients. However, the cost-effectiveness of this new regimen remains to be investigated. Objective: To evaluate the cost-effectiveness of camrelizumab combination therapy vs. chemotherapy for previously untreated patients with advanced, non-squamous NSCLC without Alk or Egfr genomic aberrations from the perspective of China's healthcare system. Methods: Based on the CameL trial, the study developed a three-health state Markov model to evaluate the cost-effectiveness of adding camrelizumab to chemotherapy compared to chemotherapy alone in NSCLC patients. The analysis models were conducted for patients unselected by PD-L1 tumor expression (the base case) and the patient subgroup with PD-L1-expressing tumors (≥1%). Primary model outcomes included the costs in US dollars and health outcomes in quality-adjusted life-years (QALYs) as well as the incremental cost-effectiveness ratio (ICER) under a willingness-to-pay threshold of $31,500 per QALY. Additionally, a scenario analysis that adjusted within-trial crossover was employed to evaluate camrelizumab combination therapy compared to chemotherapy without subsequent use of PD1/PD-L1 antibodies. Results: Camrelizumab combination therapy was more costly and provided additional 0.11 QALYs over chemotherapy in the base case analysis (0.86 vs. 0.75 QALYs), 0.12 QALYs over chemotherapy in the subgroup analysis (0.99 vs. 0.88 QALYs), and 0.34 QALYs over chemotherapy in the scenario analysis (0.86 vs. 0.52 QALYs). Correspondingly, the ICER was $63,080 per QALY, $46,311 per QALY, and $30,591 per QALY, in the base case, the subgroup, and the scenario analysis, respectively. One-way sensitivity analyses revealed that ICERs of the base case and the subgroup analysis were most sensitive to the cost of camrelizumab, the cost of pemetrexed. Besides, the base case and subgroup analysis were more sensitive to the risk of neutrophil count decreased in the camrelizumab and the utility of stable disease, respectively. Conclusion: Although camrelizumab combination therapy is not cost-effective as first-line therapy for NSCLC patients in China in the base case, adjusting within-trial crossover would move the treatment regimen toward cost-effectiveness in the scenario analysis.
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spelling pubmed-87024262021-12-25 Economic Evaluation of First-Line Camrelizumab for Advanced Non-small-cell Lung Cancer in China Xiang, Guiyuan Gu, Lingna Chen, Xuan Wang, Fan Chen, Bohua Zhao, Jie Lu, Yun Chang, Feng Zhu, Yumei Front Public Health Public Health Background: As the first domestic PD-1 antibody approved for lung cancer in China, camrelizumab has exhibited proven effectiveness for non-small-cell lung cancer (NSCLC) patients. However, the cost-effectiveness of this new regimen remains to be investigated. Objective: To evaluate the cost-effectiveness of camrelizumab combination therapy vs. chemotherapy for previously untreated patients with advanced, non-squamous NSCLC without Alk or Egfr genomic aberrations from the perspective of China's healthcare system. Methods: Based on the CameL trial, the study developed a three-health state Markov model to evaluate the cost-effectiveness of adding camrelizumab to chemotherapy compared to chemotherapy alone in NSCLC patients. The analysis models were conducted for patients unselected by PD-L1 tumor expression (the base case) and the patient subgroup with PD-L1-expressing tumors (≥1%). Primary model outcomes included the costs in US dollars and health outcomes in quality-adjusted life-years (QALYs) as well as the incremental cost-effectiveness ratio (ICER) under a willingness-to-pay threshold of $31,500 per QALY. Additionally, a scenario analysis that adjusted within-trial crossover was employed to evaluate camrelizumab combination therapy compared to chemotherapy without subsequent use of PD1/PD-L1 antibodies. Results: Camrelizumab combination therapy was more costly and provided additional 0.11 QALYs over chemotherapy in the base case analysis (0.86 vs. 0.75 QALYs), 0.12 QALYs over chemotherapy in the subgroup analysis (0.99 vs. 0.88 QALYs), and 0.34 QALYs over chemotherapy in the scenario analysis (0.86 vs. 0.52 QALYs). Correspondingly, the ICER was $63,080 per QALY, $46,311 per QALY, and $30,591 per QALY, in the base case, the subgroup, and the scenario analysis, respectively. One-way sensitivity analyses revealed that ICERs of the base case and the subgroup analysis were most sensitive to the cost of camrelizumab, the cost of pemetrexed. Besides, the base case and subgroup analysis were more sensitive to the risk of neutrophil count decreased in the camrelizumab and the utility of stable disease, respectively. Conclusion: Although camrelizumab combination therapy is not cost-effective as first-line therapy for NSCLC patients in China in the base case, adjusting within-trial crossover would move the treatment regimen toward cost-effectiveness in the scenario analysis. Frontiers Media S.A. 2021-12-10 /pmc/articles/PMC8702426/ /pubmed/34957008 http://dx.doi.org/10.3389/fpubh.2021.743558 Text en Copyright © 2021 Xiang, Gu, Chen, Wang, Chen, Zhao, Lu, Chang and Zhu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Public Health
Xiang, Guiyuan
Gu, Lingna
Chen, Xuan
Wang, Fan
Chen, Bohua
Zhao, Jie
Lu, Yun
Chang, Feng
Zhu, Yumei
Economic Evaluation of First-Line Camrelizumab for Advanced Non-small-cell Lung Cancer in China
title Economic Evaluation of First-Line Camrelizumab for Advanced Non-small-cell Lung Cancer in China
title_full Economic Evaluation of First-Line Camrelizumab for Advanced Non-small-cell Lung Cancer in China
title_fullStr Economic Evaluation of First-Line Camrelizumab for Advanced Non-small-cell Lung Cancer in China
title_full_unstemmed Economic Evaluation of First-Line Camrelizumab for Advanced Non-small-cell Lung Cancer in China
title_short Economic Evaluation of First-Line Camrelizumab for Advanced Non-small-cell Lung Cancer in China
title_sort economic evaluation of first-line camrelizumab for advanced non-small-cell lung cancer in china
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702426/
https://www.ncbi.nlm.nih.gov/pubmed/34957008
http://dx.doi.org/10.3389/fpubh.2021.743558
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