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Standard-dose osimertinib for refractory leptomeningeal metastases in T790M-positive EGFR-mutant non-small cell lung cancer

BACKGROUND: Osimertinib demonstrated promising efficacy for refractory leptomeningeal metastases (LM) in preclinical data and a clinical study at 160 mg, but there is limited data for the standard 80 mg dose. METHODS: T790M-positive patients with suspected LM after classical epidermal growth factor...

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Autores principales: Nanjo, Shigeki, Hata, Akito, Okuda, Chiyuki, Kaji, Reiko, Okada, Hideaki, Tamura, Daisuke, Irie, Kei, Okada, Hiroshi, Fukushima, Shoji, Katakami, Nobuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765232/
https://www.ncbi.nlm.nih.gov/pubmed/29190637
http://dx.doi.org/10.1038/bjc.2017.394
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author Nanjo, Shigeki
Hata, Akito
Okuda, Chiyuki
Kaji, Reiko
Okada, Hideaki
Tamura, Daisuke
Irie, Kei
Okada, Hiroshi
Fukushima, Shoji
Katakami, Nobuyuki
author_facet Nanjo, Shigeki
Hata, Akito
Okuda, Chiyuki
Kaji, Reiko
Okada, Hideaki
Tamura, Daisuke
Irie, Kei
Okada, Hiroshi
Fukushima, Shoji
Katakami, Nobuyuki
author_sort Nanjo, Shigeki
collection PubMed
description BACKGROUND: Osimertinib demonstrated promising efficacy for refractory leptomeningeal metastases (LM) in preclinical data and a clinical study at 160 mg, but there is limited data for the standard 80 mg dose. METHODS: T790M-positive patients with suspected LM after classical epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) failure were enroled. RESULTS: We investigated 13 patients (5 definitive and 8 possible LM cases). In two of the five definitive cases with T790M in and outside the central nervous system (CNS), osimertinib was effective for both lesions, with cerebrospinal fluid (CSF) clearance of cancer cells and sensitive/T790M mutations. In three definitive cases with extra-CNS T790M without CSF T790M, cancer cells and sensitive mutations in the CSF persisted after osimertinib initiation. The median progression-free survival of all 13 patients was 7.2 months. Osimertinib was generally well-tolerated despite poor performance status, but interstitial lung disease (grade 2) was confirmed in one patient. Based on 25 samples from 13 patients, the osimertinib CSF penetration rate was 2.5±0.3%. CONCLUSIONS: Osimertinib 80 mg is a useful therapeutic option for refractory LM after classical EGFR-TKI failure. It appears more effective in CSF T790M-positive cases.
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spelling pubmed-57652322019-01-01 Standard-dose osimertinib for refractory leptomeningeal metastases in T790M-positive EGFR-mutant non-small cell lung cancer Nanjo, Shigeki Hata, Akito Okuda, Chiyuki Kaji, Reiko Okada, Hideaki Tamura, Daisuke Irie, Kei Okada, Hiroshi Fukushima, Shoji Katakami, Nobuyuki Br J Cancer Clinical Study BACKGROUND: Osimertinib demonstrated promising efficacy for refractory leptomeningeal metastases (LM) in preclinical data and a clinical study at 160 mg, but there is limited data for the standard 80 mg dose. METHODS: T790M-positive patients with suspected LM after classical epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) failure were enroled. RESULTS: We investigated 13 patients (5 definitive and 8 possible LM cases). In two of the five definitive cases with T790M in and outside the central nervous system (CNS), osimertinib was effective for both lesions, with cerebrospinal fluid (CSF) clearance of cancer cells and sensitive/T790M mutations. In three definitive cases with extra-CNS T790M without CSF T790M, cancer cells and sensitive mutations in the CSF persisted after osimertinib initiation. The median progression-free survival of all 13 patients was 7.2 months. Osimertinib was generally well-tolerated despite poor performance status, but interstitial lung disease (grade 2) was confirmed in one patient. Based on 25 samples from 13 patients, the osimertinib CSF penetration rate was 2.5±0.3%. CONCLUSIONS: Osimertinib 80 mg is a useful therapeutic option for refractory LM after classical EGFR-TKI failure. It appears more effective in CSF T790M-positive cases. Nature Publishing Group 2018-01 2017-11-30 /pmc/articles/PMC5765232/ /pubmed/29190637 http://dx.doi.org/10.1038/bjc.2017.394 Text en Copyright © 2018 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Clinical Study
Nanjo, Shigeki
Hata, Akito
Okuda, Chiyuki
Kaji, Reiko
Okada, Hideaki
Tamura, Daisuke
Irie, Kei
Okada, Hiroshi
Fukushima, Shoji
Katakami, Nobuyuki
Standard-dose osimertinib for refractory leptomeningeal metastases in T790M-positive EGFR-mutant non-small cell lung cancer
title Standard-dose osimertinib for refractory leptomeningeal metastases in T790M-positive EGFR-mutant non-small cell lung cancer
title_full Standard-dose osimertinib for refractory leptomeningeal metastases in T790M-positive EGFR-mutant non-small cell lung cancer
title_fullStr Standard-dose osimertinib for refractory leptomeningeal metastases in T790M-positive EGFR-mutant non-small cell lung cancer
title_full_unstemmed Standard-dose osimertinib for refractory leptomeningeal metastases in T790M-positive EGFR-mutant non-small cell lung cancer
title_short Standard-dose osimertinib for refractory leptomeningeal metastases in T790M-positive EGFR-mutant non-small cell lung cancer
title_sort standard-dose osimertinib for refractory leptomeningeal metastases in t790m-positive egfr-mutant non-small cell lung cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765232/
https://www.ncbi.nlm.nih.gov/pubmed/29190637
http://dx.doi.org/10.1038/bjc.2017.394
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