Real‐world utility of next‐generation sequencing for targeted gene analysis and its application to treatment in lung adenocarcinoma

Abstract Purpose This study investigated the clinical utility of next‐generation sequencing (NGS) for detection of genetic alterations and its implications on treatment of lung adenocarcinoma in real‐world practice. Patients and Methods Data were reviewed for 391 patients with lung adenocarcinoma wh...

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Main Authors: Jwa Hoon Kim, Shinkyo Yoon, Dae Ho Lee, Se Jin Jang, Sung‐Min Chun, Sang‐We Kim
Format: Article
Language:English
Published: Wiley 2021-05-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.3874
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spelling doaj-1bc24c24a5f046d3bb40bf32af931d8f2021-05-16T07:45:27ZengWileyCancer Medicine2045-76342021-05-0110103197320410.1002/cam4.3874Real‐world utility of next‐generation sequencing for targeted gene analysis and its application to treatment in lung adenocarcinomaJwa Hoon Kim0Shinkyo Yoon1Dae Ho Lee2Se Jin Jang3Sung‐Min Chun4Sang‐We Kim5Department of Oncology Asan Medical Center University of Ulsan College of Medicine Seoul Republic of KoreaDepartment of Oncology Asan Medical Center University of Ulsan College of Medicine Seoul Republic of KoreaDepartment of Oncology Asan Medical Center University of Ulsan College of Medicine Seoul Republic of KoreaDepartment of Pathology Asan Medical Center University of Ulsan College of Medicine Seoul Republic of KoreaDepartment of Pathology Asan Medical Center University of Ulsan College of Medicine Seoul Republic of KoreaDepartment of Oncology Asan Medical Center University of Ulsan College of Medicine Seoul Republic of KoreaAbstract Purpose This study investigated the clinical utility of next‐generation sequencing (NGS) for detection of genetic alterations and its implications on treatment of lung adenocarcinoma in real‐world practice. Patients and Methods Data were reviewed for 391 patients with lung adenocarcinoma who underwent NGS between March 2017 and October 2018. Formalin‐fixed, paraffin‐embedded archival samples were used for performing NGS targeting 382 genes, including all exons of 199 genes, 184 hotspots, and the partial introns of 8 genes often rearranged in cancer. Survival analysis was performed for stage IV disease. Results Among the 391 patients, at least one actionable mutation was identified in 294 patients (75.2%). The most commonly mutated gene was EGFR (n = 130, 33.2%), involving EGFR exon 19 deletion (n = 48, 12.3%), L858R (n = 47, 12%), and others (n = 35, 9%), followed by KRAS (n = 48, 12.3%), ALK (n = 40, 10.2%), RET (6%), MET (3%), ROS‐1 (3%), and BRAF (2%) mutations. TP53 (46.9%) and CDKN2A (12.6%) mutations were common co‐mutations in patients with AMs. With a median follow‐up duration of 16.8 months, median overall survival was 36.8 months in patients with stage IV disease. Patients treated with the corresponding targeted therapy for AMs based on NGS reports lived significantly longer than those not treated with such therapy (p < 0.001). After multivariate analysis, targeted therapy for AM was a significantly favorable factor for survival (AM without targeted therapy vs. AM with targeted therapy, hazard ratio 2.58, 95% confidence interval 1.57–4.25; p < 0.001). Conclusion This study revealed that AMs could be comparably detected using NGS. Based on these NGS results, a suitable targeted therapy can be selected, which may improve survival in patients with lung adenocarcinoma. This NGS‐based approach is useful in real‐world practice to provide guidance when selecting targeted therapy.https://doi.org/10.1002/cam4.3874lung adenocarcinomanext‐generation sequencingsurvivaltargeted therapy
collection DOAJ
language English
format Article
sources DOAJ
author Jwa Hoon Kim
Shinkyo Yoon
Dae Ho Lee
Se Jin Jang
Sung‐Min Chun
Sang‐We Kim
spellingShingle Jwa Hoon Kim
Shinkyo Yoon
Dae Ho Lee
Se Jin Jang
Sung‐Min Chun
Sang‐We Kim
Real‐world utility of next‐generation sequencing for targeted gene analysis and its application to treatment in lung adenocarcinoma
Cancer Medicine
lung adenocarcinoma
next‐generation sequencing
survival
targeted therapy
author_facet Jwa Hoon Kim
Shinkyo Yoon
Dae Ho Lee
Se Jin Jang
Sung‐Min Chun
Sang‐We Kim
author_sort Jwa Hoon Kim
title Real‐world utility of next‐generation sequencing for targeted gene analysis and its application to treatment in lung adenocarcinoma
title_short Real‐world utility of next‐generation sequencing for targeted gene analysis and its application to treatment in lung adenocarcinoma
title_full Real‐world utility of next‐generation sequencing for targeted gene analysis and its application to treatment in lung adenocarcinoma
title_fullStr Real‐world utility of next‐generation sequencing for targeted gene analysis and its application to treatment in lung adenocarcinoma
title_full_unstemmed Real‐world utility of next‐generation sequencing for targeted gene analysis and its application to treatment in lung adenocarcinoma
title_sort real‐world utility of next‐generation sequencing for targeted gene analysis and its application to treatment in lung adenocarcinoma
publisher Wiley
series Cancer Medicine
issn 2045-7634
publishDate 2021-05-01
description Abstract Purpose This study investigated the clinical utility of next‐generation sequencing (NGS) for detection of genetic alterations and its implications on treatment of lung adenocarcinoma in real‐world practice. Patients and Methods Data were reviewed for 391 patients with lung adenocarcinoma who underwent NGS between March 2017 and October 2018. Formalin‐fixed, paraffin‐embedded archival samples were used for performing NGS targeting 382 genes, including all exons of 199 genes, 184 hotspots, and the partial introns of 8 genes often rearranged in cancer. Survival analysis was performed for stage IV disease. Results Among the 391 patients, at least one actionable mutation was identified in 294 patients (75.2%). The most commonly mutated gene was EGFR (n = 130, 33.2%), involving EGFR exon 19 deletion (n = 48, 12.3%), L858R (n = 47, 12%), and others (n = 35, 9%), followed by KRAS (n = 48, 12.3%), ALK (n = 40, 10.2%), RET (6%), MET (3%), ROS‐1 (3%), and BRAF (2%) mutations. TP53 (46.9%) and CDKN2A (12.6%) mutations were common co‐mutations in patients with AMs. With a median follow‐up duration of 16.8 months, median overall survival was 36.8 months in patients with stage IV disease. Patients treated with the corresponding targeted therapy for AMs based on NGS reports lived significantly longer than those not treated with such therapy (p < 0.001). After multivariate analysis, targeted therapy for AM was a significantly favorable factor for survival (AM without targeted therapy vs. AM with targeted therapy, hazard ratio 2.58, 95% confidence interval 1.57–4.25; p < 0.001). Conclusion This study revealed that AMs could be comparably detected using NGS. Based on these NGS results, a suitable targeted therapy can be selected, which may improve survival in patients with lung adenocarcinoma. This NGS‐based approach is useful in real‐world practice to provide guidance when selecting targeted therapy.
topic lung adenocarcinoma
next‐generation sequencing
survival
targeted therapy
url https://doi.org/10.1002/cam4.3874
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