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Cost-effectiveness of pembrolizumab for advanced non-small cell lung cancer patients with varying comorbidity burden

OBJECTIVES: While previous cost-effectiveness studies on pembrolizumab in stage IV non-small cell lung cancer (NSCLC) have found these regimens to be cost-effective, their reliance on randomized controlled trial (RCT) data with strict inclusion criteria limits generalizability to patients with comor...

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Autores principales: Criss, Steven D., Palazzo, Lauren, Watson, Tina R., Paquette, Adelle M., Sigel, Keith, Wisnivesky, Juan, Kong, Chung Yin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988966/
https://www.ncbi.nlm.nih.gov/pubmed/31995619
http://dx.doi.org/10.1371/journal.pone.0228288
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author Criss, Steven D.
Palazzo, Lauren
Watson, Tina R.
Paquette, Adelle M.
Sigel, Keith
Wisnivesky, Juan
Kong, Chung Yin
author_facet Criss, Steven D.
Palazzo, Lauren
Watson, Tina R.
Paquette, Adelle M.
Sigel, Keith
Wisnivesky, Juan
Kong, Chung Yin
author_sort Criss, Steven D.
collection PubMed
description OBJECTIVES: While previous cost-effectiveness studies on pembrolizumab in stage IV non-small cell lung cancer (NSCLC) have found these regimens to be cost-effective, their reliance on randomized controlled trial (RCT) data with strict inclusion criteria limits generalizability to patients with comorbidities. We estimated the cost-effectiveness of first-line pembrolizumab for patients with various comorbidities. MATERIALS AND METHODS: In our base case analysis, we studied pembrolizumab plus chemotherapy (pembrolizumab combination therapy) versus chemotherapy alone. In a secondary analysis, we considered only patients with PD-L1 expression of at least 50% (PD-L1-high) and evaluated pembrolizumab monotherapy, pembrolizumab combination therapy, and chemotherapy alone. Microsimulation models were developed for the base case and the PD-L1-high analyses. To estimate outcomes of patients with differing comorbidities, we combined survival data from patients with few or no comorbidities from the RCTs with estimates from the general population obtained from the Surveillance, Epidemiology, and End Results (SEER)-Medicare database. Comorbidity burden level was divided into three groups based on the Charlson score (equal to 0, 1, or 2+); patients with various other specific comorbidities were also analyzed. Incremental cost-effectiveness ratios (ICER) were compared to a willingness-to-pay (WTP) threshold of $100,000/quality-adjusted life-year (QALY). RESULTS: In the Charlson 0, Charlson 1, and Charlson 2+ patient populations, estimated ICERs for pembrolizumab combination therapy in the base case model were $173,919/QALY, $175,165/QALY, and $181,777/QALY, respectively, compared to chemotherapy. In the PD-L1-high model, the Charlson 0, Charlson 1, and Charlson 2+ patients had ICERs of $147,406/QALY, $149,026/QALY, and $154,521/QALY with pembrolizumab combination therapy versus chemotherapy. Pembrolizumab monotherapy was weakly dominated for each comorbidity group in the PD-L1-high model. CONCLUSION: For patients with stage IV NSCLC and varying comorbidity burden, first-line treatment with pembrolizumab does not represent a cost-effective strategy compared to chemotherapy. Resources should be focused on collecting immunotherapy survival data for more representative NSCLC patient populations.
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spelling pubmed-69889662020-02-04 Cost-effectiveness of pembrolizumab for advanced non-small cell lung cancer patients with varying comorbidity burden Criss, Steven D. Palazzo, Lauren Watson, Tina R. Paquette, Adelle M. Sigel, Keith Wisnivesky, Juan Kong, Chung Yin PLoS One Research Article OBJECTIVES: While previous cost-effectiveness studies on pembrolizumab in stage IV non-small cell lung cancer (NSCLC) have found these regimens to be cost-effective, their reliance on randomized controlled trial (RCT) data with strict inclusion criteria limits generalizability to patients with comorbidities. We estimated the cost-effectiveness of first-line pembrolizumab for patients with various comorbidities. MATERIALS AND METHODS: In our base case analysis, we studied pembrolizumab plus chemotherapy (pembrolizumab combination therapy) versus chemotherapy alone. In a secondary analysis, we considered only patients with PD-L1 expression of at least 50% (PD-L1-high) and evaluated pembrolizumab monotherapy, pembrolizumab combination therapy, and chemotherapy alone. Microsimulation models were developed for the base case and the PD-L1-high analyses. To estimate outcomes of patients with differing comorbidities, we combined survival data from patients with few or no comorbidities from the RCTs with estimates from the general population obtained from the Surveillance, Epidemiology, and End Results (SEER)-Medicare database. Comorbidity burden level was divided into three groups based on the Charlson score (equal to 0, 1, or 2+); patients with various other specific comorbidities were also analyzed. Incremental cost-effectiveness ratios (ICER) were compared to a willingness-to-pay (WTP) threshold of $100,000/quality-adjusted life-year (QALY). RESULTS: In the Charlson 0, Charlson 1, and Charlson 2+ patient populations, estimated ICERs for pembrolizumab combination therapy in the base case model were $173,919/QALY, $175,165/QALY, and $181,777/QALY, respectively, compared to chemotherapy. In the PD-L1-high model, the Charlson 0, Charlson 1, and Charlson 2+ patients had ICERs of $147,406/QALY, $149,026/QALY, and $154,521/QALY with pembrolizumab combination therapy versus chemotherapy. Pembrolizumab monotherapy was weakly dominated for each comorbidity group in the PD-L1-high model. CONCLUSION: For patients with stage IV NSCLC and varying comorbidity burden, first-line treatment with pembrolizumab does not represent a cost-effective strategy compared to chemotherapy. Resources should be focused on collecting immunotherapy survival data for more representative NSCLC patient populations. Public Library of Science 2020-01-29 /pmc/articles/PMC6988966/ /pubmed/31995619 http://dx.doi.org/10.1371/journal.pone.0228288 Text en © 2020 Criss et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Criss, Steven D.
Palazzo, Lauren
Watson, Tina R.
Paquette, Adelle M.
Sigel, Keith
Wisnivesky, Juan
Kong, Chung Yin
Cost-effectiveness of pembrolizumab for advanced non-small cell lung cancer patients with varying comorbidity burden
title Cost-effectiveness of pembrolizumab for advanced non-small cell lung cancer patients with varying comorbidity burden
title_full Cost-effectiveness of pembrolizumab for advanced non-small cell lung cancer patients with varying comorbidity burden
title_fullStr Cost-effectiveness of pembrolizumab for advanced non-small cell lung cancer patients with varying comorbidity burden
title_full_unstemmed Cost-effectiveness of pembrolizumab for advanced non-small cell lung cancer patients with varying comorbidity burden
title_short Cost-effectiveness of pembrolizumab for advanced non-small cell lung cancer patients with varying comorbidity burden
title_sort cost-effectiveness of pembrolizumab for advanced non-small cell lung cancer patients with varying comorbidity burden
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988966/
https://www.ncbi.nlm.nih.gov/pubmed/31995619
http://dx.doi.org/10.1371/journal.pone.0228288
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