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TAPO in first‐line osimertinib therapy and continuation of osimertinib
BACKGROUND: Osimertinib is associated with a relatively high frequency of drug‐induced interstitial lung disease (D‐ILD), and transient asymptomatic pulmonary opacities (TAPO) have been reported to occur during osimertinib administration. The frequency of TAPO during first‐line treatment and the pro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968596/ https://www.ncbi.nlm.nih.gov/pubmed/36578073 http://dx.doi.org/10.1111/1759-7714.14782 |
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author | Mimura, Chihiro Kaneshiro, Kazumi Fujimoto, Shodai Dokuni, Ryota Iwamoto, Natsuhiko Matsumura, Kanoko Hatakeyama, Yukihisa Kono, Yuko Tachihara, Motoko |
author_facet | Mimura, Chihiro Kaneshiro, Kazumi Fujimoto, Shodai Dokuni, Ryota Iwamoto, Natsuhiko Matsumura, Kanoko Hatakeyama, Yukihisa Kono, Yuko Tachihara, Motoko |
author_sort | Mimura, Chihiro |
collection | PubMed |
description | BACKGROUND: Osimertinib is associated with a relatively high frequency of drug‐induced interstitial lung disease (D‐ILD), and transient asymptomatic pulmonary opacities (TAPO) have been reported to occur during osimertinib administration. The frequency of TAPO during first‐line treatment and the pros and cons of osimertinib continuation is unknown. METHODS: This was a multicenter, retrospective study. The purpose of this study was to research the frequency of TAPO and to evaluate osimertinib continuation in first‐line therapy. We also evaluated progression‐free survival (PFS) including subgroup analysis. RESULTS: From August 2018 to December 2020, 133 patients were enrolled into the study. The median observation period was 23.2 months (0.3–48.3 months). Thirty patients (22.6%) experienced D‐ILD events, including 16 patients (12.1%) with CTCAE grade 1, five patients (3.8%) with grade 2, and nine patients (6.7%) with grade 3 and above D‐ILD. Among the patients with grade 1 D‐ILD, 11 cases (8.3%) of TAPO were observed, and all patients succeeded in osimertinib continuation. The TAPO images were characterized by localized patchy opacities (73%). The median PFS was 22.6 months (95% confidence interval [CI]: 17.8–28.7 months). Patients with TAPO had a significantly longer PFS than patients with non‐TAPO D‐ILD in the multivariate analysis. CONCLUSIONS: This study showed that grade 1 D‐ILD might include TAPO and that patients with TAPO might have good PFS. We need to consider the possibility of osimertinib continuation when lung opacities appear. |
format | Online Article Text |
id | pubmed-9968596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-99685962023-02-28 TAPO in first‐line osimertinib therapy and continuation of osimertinib Mimura, Chihiro Kaneshiro, Kazumi Fujimoto, Shodai Dokuni, Ryota Iwamoto, Natsuhiko Matsumura, Kanoko Hatakeyama, Yukihisa Kono, Yuko Tachihara, Motoko Thorac Cancer Original Articles BACKGROUND: Osimertinib is associated with a relatively high frequency of drug‐induced interstitial lung disease (D‐ILD), and transient asymptomatic pulmonary opacities (TAPO) have been reported to occur during osimertinib administration. The frequency of TAPO during first‐line treatment and the pros and cons of osimertinib continuation is unknown. METHODS: This was a multicenter, retrospective study. The purpose of this study was to research the frequency of TAPO and to evaluate osimertinib continuation in first‐line therapy. We also evaluated progression‐free survival (PFS) including subgroup analysis. RESULTS: From August 2018 to December 2020, 133 patients were enrolled into the study. The median observation period was 23.2 months (0.3–48.3 months). Thirty patients (22.6%) experienced D‐ILD events, including 16 patients (12.1%) with CTCAE grade 1, five patients (3.8%) with grade 2, and nine patients (6.7%) with grade 3 and above D‐ILD. Among the patients with grade 1 D‐ILD, 11 cases (8.3%) of TAPO were observed, and all patients succeeded in osimertinib continuation. The TAPO images were characterized by localized patchy opacities (73%). The median PFS was 22.6 months (95% confidence interval [CI]: 17.8–28.7 months). Patients with TAPO had a significantly longer PFS than patients with non‐TAPO D‐ILD in the multivariate analysis. CONCLUSIONS: This study showed that grade 1 D‐ILD might include TAPO and that patients with TAPO might have good PFS. We need to consider the possibility of osimertinib continuation when lung opacities appear. John Wiley & Sons Australia, Ltd 2022-12-28 /pmc/articles/PMC9968596/ /pubmed/36578073 http://dx.doi.org/10.1111/1759-7714.14782 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Mimura, Chihiro Kaneshiro, Kazumi Fujimoto, Shodai Dokuni, Ryota Iwamoto, Natsuhiko Matsumura, Kanoko Hatakeyama, Yukihisa Kono, Yuko Tachihara, Motoko TAPO in first‐line osimertinib therapy and continuation of osimertinib |
title |
TAPO in first‐line osimertinib therapy and continuation of osimertinib |
title_full |
TAPO in first‐line osimertinib therapy and continuation of osimertinib |
title_fullStr |
TAPO in first‐line osimertinib therapy and continuation of osimertinib |
title_full_unstemmed |
TAPO in first‐line osimertinib therapy and continuation of osimertinib |
title_short |
TAPO in first‐line osimertinib therapy and continuation of osimertinib |
title_sort | tapo in first‐line osimertinib therapy and continuation of osimertinib |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968596/ https://www.ncbi.nlm.nih.gov/pubmed/36578073 http://dx.doi.org/10.1111/1759-7714.14782 |
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