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Osimertinib as first-line treatment for recurrent lung cancer patients with EGFR mutation
BACKGROUND: Although osimertinib was approved as adjuvant therapy for lung cancer patients with EGFR mutation in various countries, there is still some ongoing debate as osimertinib has been approved based on disease-free survival (DFS) rather than overall survival (OS). We curated a case series in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636461/ https://www.ncbi.nlm.nih.gov/pubmed/37969303 http://dx.doi.org/10.21037/jtd-23-537 |
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author | Osoegawa, Atsushi Karashima, Takashi Takumi, Yohei Sato, Takahiro Abe, Miyuki Hashimoto, Takafumi Sugio, Kenji |
author_facet | Osoegawa, Atsushi Karashima, Takashi Takumi, Yohei Sato, Takahiro Abe, Miyuki Hashimoto, Takafumi Sugio, Kenji |
author_sort | Osoegawa, Atsushi |
collection | PubMed |
description | BACKGROUND: Although osimertinib was approved as adjuvant therapy for lung cancer patients with EGFR mutation in various countries, there is still some ongoing debate as osimertinib has been approved based on disease-free survival (DFS) rather than overall survival (OS). We curated a case series in which we documented patterns of recurrence and efficacy and safety of osimertinib after recurrence. METHODS: Patients who received osimertinib as first-line treatment for postoperative recurrence between September 2018 and January 2023 were included. Clinicopathological factors, duration of osimertinib treatment (DoT), and adverse events were collected and analyzed. RESULTS: Twenty patients received osimertinib [male, n=6; median age, 75 years (range, 55–85 years)]. The EGFR mutation type was L858R in 11 patients and exon 19 deletion in eight patients. The performance status (PS) was 0 or 1 in all but two patients, who had symptomatic brain metastasis and were therefore PS 3. The first site of postoperative recurrence was locoregional in five patients and distant in 15 patients, including seven with brain metastasis. As of February 2023, 10 patients were still on osimertinib, including three with brain metastasis. Patients with brain metastasis or poor PS had a considerably shorter DoT than their counterparts. Three patients with symptomatic brain metastasis or leptomeningeal metastasis initially responded to osimertinib, but all died of disease progression. Five patients discontinued osimertinib due to serious adverse effects (pneumonitis, drug eruption, and heart failure). CONCLUSIONS: Although osimertinib exerts great disease control, even in patients with brain metastasis or poor PS, their presence was associated with a poor prognosis, even with osimertinib treatment. Therefore, adjuvant osimertinib is recommended unless contraindicated. |
format | Online Article Text |
id | pubmed-10636461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-106364612023-11-15 Osimertinib as first-line treatment for recurrent lung cancer patients with EGFR mutation Osoegawa, Atsushi Karashima, Takashi Takumi, Yohei Sato, Takahiro Abe, Miyuki Hashimoto, Takafumi Sugio, Kenji J Thorac Dis Original Article BACKGROUND: Although osimertinib was approved as adjuvant therapy for lung cancer patients with EGFR mutation in various countries, there is still some ongoing debate as osimertinib has been approved based on disease-free survival (DFS) rather than overall survival (OS). We curated a case series in which we documented patterns of recurrence and efficacy and safety of osimertinib after recurrence. METHODS: Patients who received osimertinib as first-line treatment for postoperative recurrence between September 2018 and January 2023 were included. Clinicopathological factors, duration of osimertinib treatment (DoT), and adverse events were collected and analyzed. RESULTS: Twenty patients received osimertinib [male, n=6; median age, 75 years (range, 55–85 years)]. The EGFR mutation type was L858R in 11 patients and exon 19 deletion in eight patients. The performance status (PS) was 0 or 1 in all but two patients, who had symptomatic brain metastasis and were therefore PS 3. The first site of postoperative recurrence was locoregional in five patients and distant in 15 patients, including seven with brain metastasis. As of February 2023, 10 patients were still on osimertinib, including three with brain metastasis. Patients with brain metastasis or poor PS had a considerably shorter DoT than their counterparts. Three patients with symptomatic brain metastasis or leptomeningeal metastasis initially responded to osimertinib, but all died of disease progression. Five patients discontinued osimertinib due to serious adverse effects (pneumonitis, drug eruption, and heart failure). CONCLUSIONS: Although osimertinib exerts great disease control, even in patients with brain metastasis or poor PS, their presence was associated with a poor prognosis, even with osimertinib treatment. Therefore, adjuvant osimertinib is recommended unless contraindicated. AME Publishing Company 2023-10-10 2023-10-31 /pmc/articles/PMC10636461/ /pubmed/37969303 http://dx.doi.org/10.21037/jtd-23-537 Text en 2023 Journal of Thoracic Disease. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Osoegawa, Atsushi Karashima, Takashi Takumi, Yohei Sato, Takahiro Abe, Miyuki Hashimoto, Takafumi Sugio, Kenji Osimertinib as first-line treatment for recurrent lung cancer patients with EGFR mutation |
title | Osimertinib as first-line treatment for recurrent lung cancer patients with EGFR mutation |
title_full | Osimertinib as first-line treatment for recurrent lung cancer patients with EGFR mutation |
title_fullStr | Osimertinib as first-line treatment for recurrent lung cancer patients with EGFR mutation |
title_full_unstemmed | Osimertinib as first-line treatment for recurrent lung cancer patients with EGFR mutation |
title_short | Osimertinib as first-line treatment for recurrent lung cancer patients with EGFR mutation |
title_sort | osimertinib as first-line treatment for recurrent lung cancer patients with egfr mutation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636461/ https://www.ncbi.nlm.nih.gov/pubmed/37969303 http://dx.doi.org/10.21037/jtd-23-537 |
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