Cargando…

Determining the optimal PD‐1/PD‐L1 inhibitors for the first‐line treatment of non‐small‐cell lung cancer with high‐level PD‐L1 expression in China

BACKGROUND AND OBJECTIVE: The programmed death 1 and ligand (PD‐1/PD‐L1) inhibitors have significantly altered therapeutic perspectives on non‐small‐cell lung cancer (NSCLC). However, their efficacy and safety are unknown since direct clinical trials have not yet been performed on them. It is also n...

Descripción completa

Detalles Bibliográficos
Autores principales: Teng, Meng‐Meng, Chen, Si‐Ying, Yang, Bo, Wang, Yan, Han, Rui‐Ying, An, Meng‐Na, Dong, Ya‐lin, You, Hai‐Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446572/
https://www.ncbi.nlm.nih.gov/pubmed/34382361
http://dx.doi.org/10.1002/cam4.4191
_version_ 1784568910185496576
author Teng, Meng‐Meng
Chen, Si‐Ying
Yang, Bo
Wang, Yan
Han, Rui‐Ying
An, Meng‐Na
Dong, Ya‐lin
You, Hai‐Sheng
author_facet Teng, Meng‐Meng
Chen, Si‐Ying
Yang, Bo
Wang, Yan
Han, Rui‐Ying
An, Meng‐Na
Dong, Ya‐lin
You, Hai‐Sheng
author_sort Teng, Meng‐Meng
collection PubMed
description BACKGROUND AND OBJECTIVE: The programmed death 1 and ligand (PD‐1/PD‐L1) inhibitors have significantly altered therapeutic perspectives on non‐small‐cell lung cancer (NSCLC). However, their efficacy and safety are unknown since direct clinical trials have not yet been performed on them. It is also necessary to determine the economics of PD‐1/PD‐L1 inhibitors due to their high cost. The aim was to evaluate the efficacy, safety, and cost‐effectiveness of PD‐1/PD‐L1 inhibitor monotherapy for advanced NSCLC patients in China with high PD‐L1 expression as first‐line treatment. METHODS: From the PubMed, Cochrane, and Web of Science databases, we retrieved survival, progression, and safety data on PD‐1/PD‐L1 inhibitor monotherapy for advanced NSCLC patients. A network meta‐analysis (NMA) was performed to consider PD‐1/PD‐L1 inhibitors in efficacy and safety. A Markov model with a full‐lifetime horizon was adopted. Clinical and utility data were collected through the trial. The cost per quality‐adjusted life year (QALY) was as incremental cost‐effectiveness ratio (ICER). Sensitivity analyses were performed. RESULTS: This study included five phase III clinical trials using four drugs: nivolumab, pembrolizumab, atezolizumab, and durvalumab. The NMA demonstrated that the four drugs had similar efficacy and safety, while pembrolizumab and atezolizumab were better for than for nivolumab (hazard ratio (HR) = 0.66, 95% confidence intervals (CIs): 0.46–0.95 and HR = 0.59, 95%CI: 0.37–0.94) in progression‐free survival (PFS), and the risk of a severe adverse event was higher for atezolizumab than for nivolumab and pembrolizumab. Compared with nivolumab, durvalumab, pembrolizumab, and atezolizumab had QALY of 0.19, 0.38, and 0.53, respectively, which induced ICERs of $ 197,028.8/QALY, $ 111,859.0/QALY, and $ 76,182.3/QALY, respectively. CONCLUSION: The efficacy and safety are similar among types of PD‐1/PD‐L1‐inhibitor monotherapy. The cost‐effectiveness of nivolumab appears optimal, but the other PD‐1/PD‐L1 inhibitors are not as cost‐effective for the first‐line treatment of advanced NSCLC in China.
format Online
Article
Text
id pubmed-8446572
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-84465722021-09-22 Determining the optimal PD‐1/PD‐L1 inhibitors for the first‐line treatment of non‐small‐cell lung cancer with high‐level PD‐L1 expression in China Teng, Meng‐Meng Chen, Si‐Ying Yang, Bo Wang, Yan Han, Rui‐Ying An, Meng‐Na Dong, Ya‐lin You, Hai‐Sheng Cancer Med Clinical Cancer Research BACKGROUND AND OBJECTIVE: The programmed death 1 and ligand (PD‐1/PD‐L1) inhibitors have significantly altered therapeutic perspectives on non‐small‐cell lung cancer (NSCLC). However, their efficacy and safety are unknown since direct clinical trials have not yet been performed on them. It is also necessary to determine the economics of PD‐1/PD‐L1 inhibitors due to their high cost. The aim was to evaluate the efficacy, safety, and cost‐effectiveness of PD‐1/PD‐L1 inhibitor monotherapy for advanced NSCLC patients in China with high PD‐L1 expression as first‐line treatment. METHODS: From the PubMed, Cochrane, and Web of Science databases, we retrieved survival, progression, and safety data on PD‐1/PD‐L1 inhibitor monotherapy for advanced NSCLC patients. A network meta‐analysis (NMA) was performed to consider PD‐1/PD‐L1 inhibitors in efficacy and safety. A Markov model with a full‐lifetime horizon was adopted. Clinical and utility data were collected through the trial. The cost per quality‐adjusted life year (QALY) was as incremental cost‐effectiveness ratio (ICER). Sensitivity analyses were performed. RESULTS: This study included five phase III clinical trials using four drugs: nivolumab, pembrolizumab, atezolizumab, and durvalumab. The NMA demonstrated that the four drugs had similar efficacy and safety, while pembrolizumab and atezolizumab were better for than for nivolumab (hazard ratio (HR) = 0.66, 95% confidence intervals (CIs): 0.46–0.95 and HR = 0.59, 95%CI: 0.37–0.94) in progression‐free survival (PFS), and the risk of a severe adverse event was higher for atezolizumab than for nivolumab and pembrolizumab. Compared with nivolumab, durvalumab, pembrolizumab, and atezolizumab had QALY of 0.19, 0.38, and 0.53, respectively, which induced ICERs of $ 197,028.8/QALY, $ 111,859.0/QALY, and $ 76,182.3/QALY, respectively. CONCLUSION: The efficacy and safety are similar among types of PD‐1/PD‐L1‐inhibitor monotherapy. The cost‐effectiveness of nivolumab appears optimal, but the other PD‐1/PD‐L1 inhibitors are not as cost‐effective for the first‐line treatment of advanced NSCLC in China. John Wiley and Sons Inc. 2021-08-12 /pmc/articles/PMC8446572/ /pubmed/34382361 http://dx.doi.org/10.1002/cam4.4191 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Teng, Meng‐Meng
Chen, Si‐Ying
Yang, Bo
Wang, Yan
Han, Rui‐Ying
An, Meng‐Na
Dong, Ya‐lin
You, Hai‐Sheng
Determining the optimal PD‐1/PD‐L1 inhibitors for the first‐line treatment of non‐small‐cell lung cancer with high‐level PD‐L1 expression in China
title Determining the optimal PD‐1/PD‐L1 inhibitors for the first‐line treatment of non‐small‐cell lung cancer with high‐level PD‐L1 expression in China
title_full Determining the optimal PD‐1/PD‐L1 inhibitors for the first‐line treatment of non‐small‐cell lung cancer with high‐level PD‐L1 expression in China
title_fullStr Determining the optimal PD‐1/PD‐L1 inhibitors for the first‐line treatment of non‐small‐cell lung cancer with high‐level PD‐L1 expression in China
title_full_unstemmed Determining the optimal PD‐1/PD‐L1 inhibitors for the first‐line treatment of non‐small‐cell lung cancer with high‐level PD‐L1 expression in China
title_short Determining the optimal PD‐1/PD‐L1 inhibitors for the first‐line treatment of non‐small‐cell lung cancer with high‐level PD‐L1 expression in China
title_sort determining the optimal pd‐1/pd‐l1 inhibitors for the first‐line treatment of non‐small‐cell lung cancer with high‐level pd‐l1 expression in china
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446572/
https://www.ncbi.nlm.nih.gov/pubmed/34382361
http://dx.doi.org/10.1002/cam4.4191
work_keys_str_mv AT tengmengmeng determiningtheoptimalpd1pdl1inhibitorsforthefirstlinetreatmentofnonsmallcelllungcancerwithhighlevelpdl1expressioninchina
AT chensiying determiningtheoptimalpd1pdl1inhibitorsforthefirstlinetreatmentofnonsmallcelllungcancerwithhighlevelpdl1expressioninchina
AT yangbo determiningtheoptimalpd1pdl1inhibitorsforthefirstlinetreatmentofnonsmallcelllungcancerwithhighlevelpdl1expressioninchina
AT wangyan determiningtheoptimalpd1pdl1inhibitorsforthefirstlinetreatmentofnonsmallcelllungcancerwithhighlevelpdl1expressioninchina
AT hanruiying determiningtheoptimalpd1pdl1inhibitorsforthefirstlinetreatmentofnonsmallcelllungcancerwithhighlevelpdl1expressioninchina
AT anmengna determiningtheoptimalpd1pdl1inhibitorsforthefirstlinetreatmentofnonsmallcelllungcancerwithhighlevelpdl1expressioninchina
AT dongyalin determiningtheoptimalpd1pdl1inhibitorsforthefirstlinetreatmentofnonsmallcelllungcancerwithhighlevelpdl1expressioninchina
AT youhaisheng determiningtheoptimalpd1pdl1inhibitorsforthefirstlinetreatmentofnonsmallcelllungcancerwithhighlevelpdl1expressioninchina