Cargando…

Efficacy and safety of tyrosine kinase inhibitors in advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutation: a network meta-analysis

AIM: To compare the efficacy and safety of tyrosine kinase inhibitors (TKIs) as first-line treatment in patients with locally advanced or metastatic non-small-cell lung cancer (NSCLC) with positive EGFR mutation. MATERIALS & METHODS: Following a systematic literature review until December 2019,...

Descripción completa

Detalles Bibliográficos
Autores principales: Alanazi, Abdullah, Yunusa, Ismaeel, Elenizi, Khaled, Alzarea, Abdulaziz I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724735/
https://www.ncbi.nlm.nih.gov/pubmed/33318755
http://dx.doi.org/10.2217/lmt-2020-0011
_version_ 1783620582624985088
author Alanazi, Abdullah
Yunusa, Ismaeel
Elenizi, Khaled
Alzarea, Abdulaziz I
author_facet Alanazi, Abdullah
Yunusa, Ismaeel
Elenizi, Khaled
Alzarea, Abdulaziz I
author_sort Alanazi, Abdullah
collection PubMed
description AIM: To compare the efficacy and safety of tyrosine kinase inhibitors (TKIs) as first-line treatment in patients with locally advanced or metastatic non-small-cell lung cancer (NSCLC) with positive EGFR mutation. MATERIALS & METHODS: Following a systematic literature review until December 2019, we conducted a random-effects pairwise and network meta-analyses (NMA). We ranked treatments for efficacy and safety based on the surface under the cumulative ranking curve (SUCRA). RESULTS: Tyrosine kinase inhibitors of the epidermal growth factor receptor (EGFR-TKI) improved survival outcomes with fewer grade 3 or higher adverse events compared to chemotherapy. Overall survival results suggest that osimertinib has the highest probability of being the most efficacious (SUCRA, 79.9%), followed by dacomitinib (SUCRA, 75.8%). Adverse events results suggest that osimertinib (SUCRA, 84.3%) and gefitinib (SUCRA, 78.9%) has the highest probability of being the safest. CONCLUSION: In this NMA, we found that osimertinib is the most efficacious and safest EGFR-TKI. These results may guide clinicians in choosing the most appropriate treatment option among EGFR-TKIs for their patient’s individual clinical characteristics.
format Online
Article
Text
id pubmed-7724735
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Future Medicine Ltd
record_format MEDLINE/PubMed
spelling pubmed-77247352020-12-13 Efficacy and safety of tyrosine kinase inhibitors in advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutation: a network meta-analysis Alanazi, Abdullah Yunusa, Ismaeel Elenizi, Khaled Alzarea, Abdulaziz I Lung Cancer Manag Meta-Analysis AIM: To compare the efficacy and safety of tyrosine kinase inhibitors (TKIs) as first-line treatment in patients with locally advanced or metastatic non-small-cell lung cancer (NSCLC) with positive EGFR mutation. MATERIALS & METHODS: Following a systematic literature review until December 2019, we conducted a random-effects pairwise and network meta-analyses (NMA). We ranked treatments for efficacy and safety based on the surface under the cumulative ranking curve (SUCRA). RESULTS: Tyrosine kinase inhibitors of the epidermal growth factor receptor (EGFR-TKI) improved survival outcomes with fewer grade 3 or higher adverse events compared to chemotherapy. Overall survival results suggest that osimertinib has the highest probability of being the most efficacious (SUCRA, 79.9%), followed by dacomitinib (SUCRA, 75.8%). Adverse events results suggest that osimertinib (SUCRA, 84.3%) and gefitinib (SUCRA, 78.9%) has the highest probability of being the safest. CONCLUSION: In this NMA, we found that osimertinib is the most efficacious and safest EGFR-TKI. These results may guide clinicians in choosing the most appropriate treatment option among EGFR-TKIs for their patient’s individual clinical characteristics. Future Medicine Ltd 2020-11-23 /pmc/articles/PMC7724735/ /pubmed/33318755 http://dx.doi.org/10.2217/lmt-2020-0011 Text en © 2020 Abdullah Alanazi, Ismaeel Yunusa and Khaled Elenizi This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Meta-Analysis
Alanazi, Abdullah
Yunusa, Ismaeel
Elenizi, Khaled
Alzarea, Abdulaziz I
Efficacy and safety of tyrosine kinase inhibitors in advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutation: a network meta-analysis
title Efficacy and safety of tyrosine kinase inhibitors in advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutation: a network meta-analysis
title_full Efficacy and safety of tyrosine kinase inhibitors in advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutation: a network meta-analysis
title_fullStr Efficacy and safety of tyrosine kinase inhibitors in advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutation: a network meta-analysis
title_full_unstemmed Efficacy and safety of tyrosine kinase inhibitors in advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutation: a network meta-analysis
title_short Efficacy and safety of tyrosine kinase inhibitors in advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutation: a network meta-analysis
title_sort efficacy and safety of tyrosine kinase inhibitors in advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutation: a network meta-analysis
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724735/
https://www.ncbi.nlm.nih.gov/pubmed/33318755
http://dx.doi.org/10.2217/lmt-2020-0011
work_keys_str_mv AT alanaziabdullah efficacyandsafetyoftyrosinekinaseinhibitorsinadvancednonsmallcelllungcancerharboringepidermalgrowthfactorreceptormutationanetworkmetaanalysis
AT yunusaismaeel efficacyandsafetyoftyrosinekinaseinhibitorsinadvancednonsmallcelllungcancerharboringepidermalgrowthfactorreceptormutationanetworkmetaanalysis
AT elenizikhaled efficacyandsafetyoftyrosinekinaseinhibitorsinadvancednonsmallcelllungcancerharboringepidermalgrowthfactorreceptormutationanetworkmetaanalysis
AT alzareaabdulazizi efficacyandsafetyoftyrosinekinaseinhibitorsinadvancednonsmallcelllungcancerharboringepidermalgrowthfactorreceptormutationanetworkmetaanalysis