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Efficacy and safety of osimertinib for leptomeningeal metastases from EGFR-mutant non-small cell lung cancer: a pooled analysis
BACKGROUND: The aim of this study was to evaluate the efficacy and safety of osimertinib for the treatment of leptomeningeal metastases (LM) from epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC). METHODS: We conducted a systematic review and meta-analysis to aggregat...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403821/ https://www.ncbi.nlm.nih.gov/pubmed/37542339 http://dx.doi.org/10.1186/s40001-023-01219-y |
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author | Wen, Lei Zhen, Junjie Shan, Changguo Lai, Mingyao Hong, Weiping Wang, Hui Ye, Mingting Yang, Yanying Li, Shaoqun Zhou, Zhaoming Zhou, Jiangfen Hu, Qingjun Li, Juan Tian, Xuwei Chen, Longhua Cai, Linbo Xie, Zhanhong Zhou, Cheng |
author_facet | Wen, Lei Zhen, Junjie Shan, Changguo Lai, Mingyao Hong, Weiping Wang, Hui Ye, Mingting Yang, Yanying Li, Shaoqun Zhou, Zhaoming Zhou, Jiangfen Hu, Qingjun Li, Juan Tian, Xuwei Chen, Longhua Cai, Linbo Xie, Zhanhong Zhou, Cheng |
author_sort | Wen, Lei |
collection | PubMed |
description | BACKGROUND: The aim of this study was to evaluate the efficacy and safety of osimertinib for the treatment of leptomeningeal metastases (LM) from epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC). METHODS: We conducted a systematic review and meta-analysis to aggregate the clinical outcomes of patients with LM from EGFR-mutant NSCLC treated with osimertinib. A comprehensive literature search for published and unpublished studies was implemented in April 2021 of PubMed, EMBASE, the Cochrane Library, and several international conference databases, in accordance with the PRISMA guidelines. Meta-analysis of proportions was conducted to calculate the pooled rate of overall response rate (ORR), disease control rate (DCR), one-year overall survival (OS), and adverse events (AEs). RESULTS: A total of eleven studies (five prospective and six retrospective) including 353 patients were included. The majority of patients (346/353, 98.0%) received osimertinib as ≥ 2nd-line treatment for LM, either at a dosage of 80 mg (161/353, 45.6%) or 160 mg (191/353, 54.1%). The pooled rates of ORR and DCR were 42% (95% CI 24% to 59%) and 93% (95% CI 88% to 97%), respectively. The pooled one-year OS rate was 59% (95% CI 53% to 65%) in 233 patients from five studies. The highest incidence of AEs of all grades was rash (53%), followed by diarrhea (45%), paronychia (35%), decreased appetite (35%), and dry skin (27%), based on data from four studies. CONCLUSIONS: Our study highlighted and confirmed the meaningful efficacy and a manageable safety profile of osimertinib for the treatment of LM from EGFR-mutant advanced NSCLC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40001-023-01219-y. |
format | Online Article Text |
id | pubmed-10403821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104038212023-08-06 Efficacy and safety of osimertinib for leptomeningeal metastases from EGFR-mutant non-small cell lung cancer: a pooled analysis Wen, Lei Zhen, Junjie Shan, Changguo Lai, Mingyao Hong, Weiping Wang, Hui Ye, Mingting Yang, Yanying Li, Shaoqun Zhou, Zhaoming Zhou, Jiangfen Hu, Qingjun Li, Juan Tian, Xuwei Chen, Longhua Cai, Linbo Xie, Zhanhong Zhou, Cheng Eur J Med Res Research BACKGROUND: The aim of this study was to evaluate the efficacy and safety of osimertinib for the treatment of leptomeningeal metastases (LM) from epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC). METHODS: We conducted a systematic review and meta-analysis to aggregate the clinical outcomes of patients with LM from EGFR-mutant NSCLC treated with osimertinib. A comprehensive literature search for published and unpublished studies was implemented in April 2021 of PubMed, EMBASE, the Cochrane Library, and several international conference databases, in accordance with the PRISMA guidelines. Meta-analysis of proportions was conducted to calculate the pooled rate of overall response rate (ORR), disease control rate (DCR), one-year overall survival (OS), and adverse events (AEs). RESULTS: A total of eleven studies (five prospective and six retrospective) including 353 patients were included. The majority of patients (346/353, 98.0%) received osimertinib as ≥ 2nd-line treatment for LM, either at a dosage of 80 mg (161/353, 45.6%) or 160 mg (191/353, 54.1%). The pooled rates of ORR and DCR were 42% (95% CI 24% to 59%) and 93% (95% CI 88% to 97%), respectively. The pooled one-year OS rate was 59% (95% CI 53% to 65%) in 233 patients from five studies. The highest incidence of AEs of all grades was rash (53%), followed by diarrhea (45%), paronychia (35%), decreased appetite (35%), and dry skin (27%), based on data from four studies. CONCLUSIONS: Our study highlighted and confirmed the meaningful efficacy and a manageable safety profile of osimertinib for the treatment of LM from EGFR-mutant advanced NSCLC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40001-023-01219-y. BioMed Central 2023-08-04 /pmc/articles/PMC10403821/ /pubmed/37542339 http://dx.doi.org/10.1186/s40001-023-01219-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wen, Lei Zhen, Junjie Shan, Changguo Lai, Mingyao Hong, Weiping Wang, Hui Ye, Mingting Yang, Yanying Li, Shaoqun Zhou, Zhaoming Zhou, Jiangfen Hu, Qingjun Li, Juan Tian, Xuwei Chen, Longhua Cai, Linbo Xie, Zhanhong Zhou, Cheng Efficacy and safety of osimertinib for leptomeningeal metastases from EGFR-mutant non-small cell lung cancer: a pooled analysis |
title | Efficacy and safety of osimertinib for leptomeningeal metastases from EGFR-mutant non-small cell lung cancer: a pooled analysis |
title_full | Efficacy and safety of osimertinib for leptomeningeal metastases from EGFR-mutant non-small cell lung cancer: a pooled analysis |
title_fullStr | Efficacy and safety of osimertinib for leptomeningeal metastases from EGFR-mutant non-small cell lung cancer: a pooled analysis |
title_full_unstemmed | Efficacy and safety of osimertinib for leptomeningeal metastases from EGFR-mutant non-small cell lung cancer: a pooled analysis |
title_short | Efficacy and safety of osimertinib for leptomeningeal metastases from EGFR-mutant non-small cell lung cancer: a pooled analysis |
title_sort | efficacy and safety of osimertinib for leptomeningeal metastases from egfr-mutant non-small cell lung cancer: a pooled analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403821/ https://www.ncbi.nlm.nih.gov/pubmed/37542339 http://dx.doi.org/10.1186/s40001-023-01219-y |
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