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Response to trametinib in a nonsmall cell lung cancer patient with osimertinib resistance harboring GNAS R201C and R201H mutations: a case report

Osimertinib, an orally administered third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, is widely approved for the first-line and second-line treatment of advanced non-small-cell lung cancer (NSCLC) with EGFR mutations. However, the rapid development of osimertinib re...

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Autores principales: Lv, You, Zhou, Chao, Chen, Zhonghai, Zhao, Xiaokai, Sun, Yonghua, Li, Jieyi, Gong, Ziying, Zhang, Daoyun, Huang, Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481290/
https://www.ncbi.nlm.nih.gov/pubmed/35946511
http://dx.doi.org/10.1097/CAD.0000000000001342
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author Lv, You
Zhou, Chao
Chen, Zhonghai
Zhao, Xiaokai
Sun, Yonghua
Li, Jieyi
Gong, Ziying
Zhang, Daoyun
Huang, Hai
author_facet Lv, You
Zhou, Chao
Chen, Zhonghai
Zhao, Xiaokai
Sun, Yonghua
Li, Jieyi
Gong, Ziying
Zhang, Daoyun
Huang, Hai
author_sort Lv, You
collection PubMed
description Osimertinib, an orally administered third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, is widely approved for the first-line and second-line treatment of advanced non-small-cell lung cancer (NSCLC) with EGFR mutations. However, the rapid development of osimertinib resistance renders the unsustainable treatment benefit. Patients with EGFR-mutated NSCLC who develop osimertinib resistance, especially those acquiring relatively rare and ‘off-target’ resistance mutations, still lack effective therapeutic options for postosimertinib therapy. Herein, we reported a 73-year-old woman diagnosed with T1N3M1 lung adenocarcinoma harboring EGFR L858R mutation, who acquired two GNAS mutations (R201C and R201H) and lost the EGFR L858R mutation after progression on icotinib and osimertinib. The patient was subsequently treated with trametinib and there was no obvious tumor increase. Our study revealed that GNAS R201 can confer the osimertinib resistance in EGFR-positive NSCLC, and present the first report of the prevalence of GNAS R201C and R201H mutants in NSCLC which response to trametinib treatment. Our case suggests that trametinib could be a treatment option in NSCLC patients harboring GNAS-activating mutations.
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spelling pubmed-94812902022-09-21 Response to trametinib in a nonsmall cell lung cancer patient with osimertinib resistance harboring GNAS R201C and R201H mutations: a case report Lv, You Zhou, Chao Chen, Zhonghai Zhao, Xiaokai Sun, Yonghua Li, Jieyi Gong, Ziying Zhang, Daoyun Huang, Hai Anticancer Drugs Case Reports Osimertinib, an orally administered third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, is widely approved for the first-line and second-line treatment of advanced non-small-cell lung cancer (NSCLC) with EGFR mutations. However, the rapid development of osimertinib resistance renders the unsustainable treatment benefit. Patients with EGFR-mutated NSCLC who develop osimertinib resistance, especially those acquiring relatively rare and ‘off-target’ resistance mutations, still lack effective therapeutic options for postosimertinib therapy. Herein, we reported a 73-year-old woman diagnosed with T1N3M1 lung adenocarcinoma harboring EGFR L858R mutation, who acquired two GNAS mutations (R201C and R201H) and lost the EGFR L858R mutation after progression on icotinib and osimertinib. The patient was subsequently treated with trametinib and there was no obvious tumor increase. Our study revealed that GNAS R201 can confer the osimertinib resistance in EGFR-positive NSCLC, and present the first report of the prevalence of GNAS R201C and R201H mutants in NSCLC which response to trametinib treatment. Our case suggests that trametinib could be a treatment option in NSCLC patients harboring GNAS-activating mutations. Lippincott Williams & Wilkins 2022-08-09 2022-10 /pmc/articles/PMC9481290/ /pubmed/35946511 http://dx.doi.org/10.1097/CAD.0000000000001342 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Case Reports
Lv, You
Zhou, Chao
Chen, Zhonghai
Zhao, Xiaokai
Sun, Yonghua
Li, Jieyi
Gong, Ziying
Zhang, Daoyun
Huang, Hai
Response to trametinib in a nonsmall cell lung cancer patient with osimertinib resistance harboring GNAS R201C and R201H mutations: a case report
title Response to trametinib in a nonsmall cell lung cancer patient with osimertinib resistance harboring GNAS R201C and R201H mutations: a case report
title_full Response to trametinib in a nonsmall cell lung cancer patient with osimertinib resistance harboring GNAS R201C and R201H mutations: a case report
title_fullStr Response to trametinib in a nonsmall cell lung cancer patient with osimertinib resistance harboring GNAS R201C and R201H mutations: a case report
title_full_unstemmed Response to trametinib in a nonsmall cell lung cancer patient with osimertinib resistance harboring GNAS R201C and R201H mutations: a case report
title_short Response to trametinib in a nonsmall cell lung cancer patient with osimertinib resistance harboring GNAS R201C and R201H mutations: a case report
title_sort response to trametinib in a nonsmall cell lung cancer patient with osimertinib resistance harboring gnas r201c and r201h mutations: a case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481290/
https://www.ncbi.nlm.nih.gov/pubmed/35946511
http://dx.doi.org/10.1097/CAD.0000000000001342
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