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Prospective exosome-focused translational research for afatinib (EXTRA) study of patients with nonsmall cell lung cancer harboring EGFR mutation: an observational clinical study
BACKGROUND: The exosome-focused translational research for afatinib (EXTRA) study is the first trial to identify novel predictive biomarkers for longer treatment efficacy of afatinib in patients with epidermal growth factor receptor (EGFR) mutation-positive nonsmall cell lung cancer (NSCLC) via a co...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262622/ https://www.ncbi.nlm.nih.gov/pubmed/37323187 http://dx.doi.org/10.1177/17588359231177021 |
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author | Takata, Saori Morikawa, Kei Tanaka, Hisashi Itani, Hidetoshi Ishihara, Masashi Horiuchi, Kazuya Kato, Yasuhiro Ikemura, Shinnosuke Nakagawa, Hideyuki Nakahara, Yoshiro Seki, Yoshitaka Bessho, Akihiro Takahashi, Nobumasa Hayashi, Kentaro Endo, Takeo Takeyama, Kiyoshi Maekura, Toshiya Takigawa, Nagio Kawase, Akikazu Endoh, Makoto Nemoto, Kenji Kishi, Kazuma Soejima, Kenzo Okuma, Yusuke Yoshimura, Kenichi Saigusa, Daisuke Kanai, Yae Ueda, Koji Togashi, Akira Matsutani, Noriyuki Seki, Nobuhiko |
author_facet | Takata, Saori Morikawa, Kei Tanaka, Hisashi Itani, Hidetoshi Ishihara, Masashi Horiuchi, Kazuya Kato, Yasuhiro Ikemura, Shinnosuke Nakagawa, Hideyuki Nakahara, Yoshiro Seki, Yoshitaka Bessho, Akihiro Takahashi, Nobumasa Hayashi, Kentaro Endo, Takeo Takeyama, Kiyoshi Maekura, Toshiya Takigawa, Nagio Kawase, Akikazu Endoh, Makoto Nemoto, Kenji Kishi, Kazuma Soejima, Kenzo Okuma, Yusuke Yoshimura, Kenichi Saigusa, Daisuke Kanai, Yae Ueda, Koji Togashi, Akira Matsutani, Noriyuki Seki, Nobuhiko |
author_sort | Takata, Saori |
collection | PubMed |
description | BACKGROUND: The exosome-focused translational research for afatinib (EXTRA) study is the first trial to identify novel predictive biomarkers for longer treatment efficacy of afatinib in patients with epidermal growth factor receptor (EGFR) mutation-positive nonsmall cell lung cancer (NSCLC) via a comprehensive association study using genomic, proteomic, epigenomic, and metabolomic analyses. OBJECTIVES: We report details of the clinical portion prior to omics analyses. DESIGN: A prospective, single-arm, observational study was conducted using afatinib 40 mg/day as an initial dose in untreated patients with EGFR mutation-positive NSCLC. Dose reduction to 20 mg every other day was allowed. METHODS: Progression-free survival (PFS), overall survival (OS), and adverse events (AEs) were evaluated. RESULTS: A total of 103 patients (median age 70 years, range 42–88 years) were enrolled from 21 institutions in Japan between February 2017 and March 2018. After a median follow-up of 35.0 months, 21% remained on afatinib treatment, whereas 9% had discontinued treatment because of AEs. The median PFS was 18.4 months, with a 3-year PFS rate of 23.3%. The median afatinib treatment duration in patients with final doses of 40 (n = 27), 30 (n = 23), and 20 mg/day (n = 35), and 20 mg every other day (n = 18) were 13.4, 15.4, 18.8, and 18.3 months, respectively. The median OS was not reached, with a 3-year OS rate of 58.5%. The median OS in patients who did (n = 25) and did not (n = 78) receive osimertinib during the entire course of treatment were 42.4 months and not reached, respectively (p = 0.654). CONCLUSIONS: As the largest prospective study in Japan, this study confirmed favorable OS following first-line afatinib in patients with EGFR mutation-positive NSCLC in a real-world setting. Further analysis of the EXTRA study is expected to identify novel predictive biomarkers for afatinib. TRIAL REGISTRATION: UMIN-CTR identifier (UMIN000024935, https://center6.umin.ac.jp/cgi-open-bin/ctr/ctr_his_list.cgi?recptno=R000028688 |
format | Online Article Text |
id | pubmed-10262622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-102626222023-06-15 Prospective exosome-focused translational research for afatinib (EXTRA) study of patients with nonsmall cell lung cancer harboring EGFR mutation: an observational clinical study Takata, Saori Morikawa, Kei Tanaka, Hisashi Itani, Hidetoshi Ishihara, Masashi Horiuchi, Kazuya Kato, Yasuhiro Ikemura, Shinnosuke Nakagawa, Hideyuki Nakahara, Yoshiro Seki, Yoshitaka Bessho, Akihiro Takahashi, Nobumasa Hayashi, Kentaro Endo, Takeo Takeyama, Kiyoshi Maekura, Toshiya Takigawa, Nagio Kawase, Akikazu Endoh, Makoto Nemoto, Kenji Kishi, Kazuma Soejima, Kenzo Okuma, Yusuke Yoshimura, Kenichi Saigusa, Daisuke Kanai, Yae Ueda, Koji Togashi, Akira Matsutani, Noriyuki Seki, Nobuhiko Ther Adv Med Oncol Original Research BACKGROUND: The exosome-focused translational research for afatinib (EXTRA) study is the first trial to identify novel predictive biomarkers for longer treatment efficacy of afatinib in patients with epidermal growth factor receptor (EGFR) mutation-positive nonsmall cell lung cancer (NSCLC) via a comprehensive association study using genomic, proteomic, epigenomic, and metabolomic analyses. OBJECTIVES: We report details of the clinical portion prior to omics analyses. DESIGN: A prospective, single-arm, observational study was conducted using afatinib 40 mg/day as an initial dose in untreated patients with EGFR mutation-positive NSCLC. Dose reduction to 20 mg every other day was allowed. METHODS: Progression-free survival (PFS), overall survival (OS), and adverse events (AEs) were evaluated. RESULTS: A total of 103 patients (median age 70 years, range 42–88 years) were enrolled from 21 institutions in Japan between February 2017 and March 2018. After a median follow-up of 35.0 months, 21% remained on afatinib treatment, whereas 9% had discontinued treatment because of AEs. The median PFS was 18.4 months, with a 3-year PFS rate of 23.3%. The median afatinib treatment duration in patients with final doses of 40 (n = 27), 30 (n = 23), and 20 mg/day (n = 35), and 20 mg every other day (n = 18) were 13.4, 15.4, 18.8, and 18.3 months, respectively. The median OS was not reached, with a 3-year OS rate of 58.5%. The median OS in patients who did (n = 25) and did not (n = 78) receive osimertinib during the entire course of treatment were 42.4 months and not reached, respectively (p = 0.654). CONCLUSIONS: As the largest prospective study in Japan, this study confirmed favorable OS following first-line afatinib in patients with EGFR mutation-positive NSCLC in a real-world setting. Further analysis of the EXTRA study is expected to identify novel predictive biomarkers for afatinib. TRIAL REGISTRATION: UMIN-CTR identifier (UMIN000024935, https://center6.umin.ac.jp/cgi-open-bin/ctr/ctr_his_list.cgi?recptno=R000028688 SAGE Publications 2023-06-05 /pmc/articles/PMC10262622/ /pubmed/37323187 http://dx.doi.org/10.1177/17588359231177021 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Takata, Saori Morikawa, Kei Tanaka, Hisashi Itani, Hidetoshi Ishihara, Masashi Horiuchi, Kazuya Kato, Yasuhiro Ikemura, Shinnosuke Nakagawa, Hideyuki Nakahara, Yoshiro Seki, Yoshitaka Bessho, Akihiro Takahashi, Nobumasa Hayashi, Kentaro Endo, Takeo Takeyama, Kiyoshi Maekura, Toshiya Takigawa, Nagio Kawase, Akikazu Endoh, Makoto Nemoto, Kenji Kishi, Kazuma Soejima, Kenzo Okuma, Yusuke Yoshimura, Kenichi Saigusa, Daisuke Kanai, Yae Ueda, Koji Togashi, Akira Matsutani, Noriyuki Seki, Nobuhiko Prospective exosome-focused translational research for afatinib (EXTRA) study of patients with nonsmall cell lung cancer harboring EGFR mutation: an observational clinical study |
title | Prospective exosome-focused translational research for afatinib (EXTRA) study of patients with nonsmall cell lung cancer harboring EGFR mutation: an observational clinical study |
title_full | Prospective exosome-focused translational research for afatinib (EXTRA) study of patients with nonsmall cell lung cancer harboring EGFR mutation: an observational clinical study |
title_fullStr | Prospective exosome-focused translational research for afatinib (EXTRA) study of patients with nonsmall cell lung cancer harboring EGFR mutation: an observational clinical study |
title_full_unstemmed | Prospective exosome-focused translational research for afatinib (EXTRA) study of patients with nonsmall cell lung cancer harboring EGFR mutation: an observational clinical study |
title_short | Prospective exosome-focused translational research for afatinib (EXTRA) study of patients with nonsmall cell lung cancer harboring EGFR mutation: an observational clinical study |
title_sort | prospective exosome-focused translational research for afatinib (extra) study of patients with nonsmall cell lung cancer harboring egfr mutation: an observational clinical study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262622/ https://www.ncbi.nlm.nih.gov/pubmed/37323187 http://dx.doi.org/10.1177/17588359231177021 |
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