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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
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
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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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