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Biomarker testing for personalized, first-line therapy in advanced nonsquamous non-small cell lung cancer patients in the real world setting in Japan: a retrospective, multicenter, observational study (the BRAVE study)
BACKGROUND: Molecular diagnostic testing is necessary to guide optimal first-line treatment. The number of patients who receive first-line treatment based on biomarker analysis in Japan is unknown. We aimed to determine the proportion of nonsquamous non-small cell lung cancer (NSCLC) patients for wh...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036489/ https://www.ncbi.nlm.nih.gov/pubmed/32127924 http://dx.doi.org/10.1177/1758835920904522 |
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author | Shimizu, Junichi Masago, Katsuhiro Saito, Haruhiro Nishino, Kazumi Kurata, Takayasu Itoh, Yohji Yoshimura, Yoko Yabuki, Yutaka Dosaka-Akita, Hirotoshi |
author_facet | Shimizu, Junichi Masago, Katsuhiro Saito, Haruhiro Nishino, Kazumi Kurata, Takayasu Itoh, Yohji Yoshimura, Yoko Yabuki, Yutaka Dosaka-Akita, Hirotoshi |
author_sort | Shimizu, Junichi |
collection | PubMed |
description | BACKGROUND: Molecular diagnostic testing is necessary to guide optimal first-line treatment. The number of patients who receive first-line treatment based on biomarker analysis in Japan is unknown. We aimed to determine the proportion of nonsquamous non-small cell lung cancer (NSCLC) patients for whom first-line treatment was selected based on biomarker testing. METHODS: This retrospective, multicenter, observational study registered patients aged ⩾20 years with locally advanced or metastatic nonsquamous NSCLC who started first-line treatment between August and December 2017 in Japan. Data were collected from medical records between January and May 2018. The primary endpoint was the proportion of patients with confirmed biomarker status for first-line treatment decision. RESULTS: Among 202 patients enrolled from 11 centers, 161 (79.7%; 95% confidence interval, 74.2–85.2%) had confirmed biomarker status. The testing rate was highest for epidermal growth factor receptor (EGFR; 97.5%), followed by anaplastic lymphoma kinase (ALK; 88.1%), programmed death ligand-1 (PD-L1; 87.1%), and ROS1 (67.3%). For first-line treatment, 70/75 patients with EGFR-positive tumors were administered an EGFR-TKI; 14/15 patients with ALK-positive tumors received an ALK inhibitor; 2/2 patients with ROS1-positive tumors received a ROS1 inhibitor; and 29/36 driver mutation-negative patients with a PD-L1 tumor proportion score ⩾50% were administered an anti-PD-1 monoclonal antibody. Median times from confirmed diagnosis date to first-line treatment initiation, and from first biomarker test order to last biomarker test result were 19 and 11 days, respectively. CONCLUSIONS: The proportion of nonsquamous NSCLC patients with confirmed biomarker status for first-line treatment was considered insufficient and in need of improvement. |
format | Online Article Text |
id | pubmed-7036489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-70364892020-03-03 Biomarker testing for personalized, first-line therapy in advanced nonsquamous non-small cell lung cancer patients in the real world setting in Japan: a retrospective, multicenter, observational study (the BRAVE study) Shimizu, Junichi Masago, Katsuhiro Saito, Haruhiro Nishino, Kazumi Kurata, Takayasu Itoh, Yohji Yoshimura, Yoko Yabuki, Yutaka Dosaka-Akita, Hirotoshi Ther Adv Med Oncol Original Research BACKGROUND: Molecular diagnostic testing is necessary to guide optimal first-line treatment. The number of patients who receive first-line treatment based on biomarker analysis in Japan is unknown. We aimed to determine the proportion of nonsquamous non-small cell lung cancer (NSCLC) patients for whom first-line treatment was selected based on biomarker testing. METHODS: This retrospective, multicenter, observational study registered patients aged ⩾20 years with locally advanced or metastatic nonsquamous NSCLC who started first-line treatment between August and December 2017 in Japan. Data were collected from medical records between January and May 2018. The primary endpoint was the proportion of patients with confirmed biomarker status for first-line treatment decision. RESULTS: Among 202 patients enrolled from 11 centers, 161 (79.7%; 95% confidence interval, 74.2–85.2%) had confirmed biomarker status. The testing rate was highest for epidermal growth factor receptor (EGFR; 97.5%), followed by anaplastic lymphoma kinase (ALK; 88.1%), programmed death ligand-1 (PD-L1; 87.1%), and ROS1 (67.3%). For first-line treatment, 70/75 patients with EGFR-positive tumors were administered an EGFR-TKI; 14/15 patients with ALK-positive tumors received an ALK inhibitor; 2/2 patients with ROS1-positive tumors received a ROS1 inhibitor; and 29/36 driver mutation-negative patients with a PD-L1 tumor proportion score ⩾50% were administered an anti-PD-1 monoclonal antibody. Median times from confirmed diagnosis date to first-line treatment initiation, and from first biomarker test order to last biomarker test result were 19 and 11 days, respectively. CONCLUSIONS: The proportion of nonsquamous NSCLC patients with confirmed biomarker status for first-line treatment was considered insufficient and in need of improvement. SAGE Publications 2020-02-22 /pmc/articles/PMC7036489/ /pubmed/32127924 http://dx.doi.org/10.1177/1758835920904522 Text en © The Author(s), 2020 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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Shimizu, Junichi Masago, Katsuhiro Saito, Haruhiro Nishino, Kazumi Kurata, Takayasu Itoh, Yohji Yoshimura, Yoko Yabuki, Yutaka Dosaka-Akita, Hirotoshi Biomarker testing for personalized, first-line therapy in advanced nonsquamous non-small cell lung cancer patients in the real world setting in Japan: a retrospective, multicenter, observational study (the BRAVE study) |
title | Biomarker testing for personalized, first-line therapy in advanced
nonsquamous non-small cell lung cancer patients in the real world setting in
Japan: a retrospective, multicenter, observational study (the BRAVE
study) |
title_full | Biomarker testing for personalized, first-line therapy in advanced
nonsquamous non-small cell lung cancer patients in the real world setting in
Japan: a retrospective, multicenter, observational study (the BRAVE
study) |
title_fullStr | Biomarker testing for personalized, first-line therapy in advanced
nonsquamous non-small cell lung cancer patients in the real world setting in
Japan: a retrospective, multicenter, observational study (the BRAVE
study) |
title_full_unstemmed | Biomarker testing for personalized, first-line therapy in advanced
nonsquamous non-small cell lung cancer patients in the real world setting in
Japan: a retrospective, multicenter, observational study (the BRAVE
study) |
title_short | Biomarker testing for personalized, first-line therapy in advanced
nonsquamous non-small cell lung cancer patients in the real world setting in
Japan: a retrospective, multicenter, observational study (the BRAVE
study) |
title_sort | biomarker testing for personalized, first-line therapy in advanced
nonsquamous non-small cell lung cancer patients in the real world setting in
japan: a retrospective, multicenter, observational study (the brave
study) |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036489/ https://www.ncbi.nlm.nih.gov/pubmed/32127924 http://dx.doi.org/10.1177/1758835920904522 |
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