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Lung cancer in young adults aged 35 years or younger: A full-scale analysis and review

Objectives: Lung cancer in young adults is a distinct disease with particular socioeconomic implications. This study aimed to clarify the clinicopathological characteristics, best interventions, and outcomes of this distinctive entity. Methods: A retrospective review of patients with lung cancer was...

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Autores principales: Liu, Bailong, Quan, Xiaoyue, Xu, Changgen, Lv, Jincai, Li, Cheng, Dong, Lihua, Liu, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6603399/
https://www.ncbi.nlm.nih.gov/pubmed/31293660
http://dx.doi.org/10.7150/jca.27490
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author Liu, Bailong
Quan, Xiaoyue
Xu, Changgen
Lv, Jincai
Li, Cheng
Dong, Lihua
Liu, Min
author_facet Liu, Bailong
Quan, Xiaoyue
Xu, Changgen
Lv, Jincai
Li, Cheng
Dong, Lihua
Liu, Min
author_sort Liu, Bailong
collection PubMed
description Objectives: Lung cancer in young adults is a distinct disease with particular socioeconomic implications. This study aimed to clarify the clinicopathological characteristics, best interventions, and outcomes of this distinctive entity. Methods: A retrospective review of patients with lung cancer was performed in our institute from January 2010 to June 2017. Young adults were defined as between 18 and 35 years old. Demographic, clinicopathological, therapeutic, and prognostic data were systematically analyzed. Results: From a total of 8734 patients, 120 (1.37%) were young adults, of which 82 with complete hospital records were included in this study. A high proportion had adenocarcinoma (45%) and late-stage disease (49.21% stage IV at diagnosis). Pleura (38.71%) were the most common metastatic site, followed by bone (35.48%) and lung (25.81%). The majority (68%) had single organ metastasis. Young patients had an increased frequency of gene mutations. Among the 18 patients for whom epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) status was determined, 10 had sensitive EGFR mutations while 5 had ALK rearrangement; only 3 patients were driver gene mutation-negative. The 1-year overall survival (OS) rate was 62.31% and the 3- and 5-year survival rates were both 53.31%; median OS was not achieved (range, 3-86 months). Male sex, negative or unknown gene mutation status, stage IV, and squamous or small cell lung cancer were associated with poor prognosis (OS) in early-onset lung cancer. Conclusions: Lung cancer in young adults is distinctive, with adenocarcinoma and stage IV at presentation being predominant characteristics. Gene mutation assessment should be mandatory in this subgroup due to the increased likelihood of positive driver gene alterations, as individualized targeted therapy may achieve superior outcomes.
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spelling pubmed-66033992019-07-10 Lung cancer in young adults aged 35 years or younger: A full-scale analysis and review Liu, Bailong Quan, Xiaoyue Xu, Changgen Lv, Jincai Li, Cheng Dong, Lihua Liu, Min J Cancer Review Objectives: Lung cancer in young adults is a distinct disease with particular socioeconomic implications. This study aimed to clarify the clinicopathological characteristics, best interventions, and outcomes of this distinctive entity. Methods: A retrospective review of patients with lung cancer was performed in our institute from January 2010 to June 2017. Young adults were defined as between 18 and 35 years old. Demographic, clinicopathological, therapeutic, and prognostic data were systematically analyzed. Results: From a total of 8734 patients, 120 (1.37%) were young adults, of which 82 with complete hospital records were included in this study. A high proportion had adenocarcinoma (45%) and late-stage disease (49.21% stage IV at diagnosis). Pleura (38.71%) were the most common metastatic site, followed by bone (35.48%) and lung (25.81%). The majority (68%) had single organ metastasis. Young patients had an increased frequency of gene mutations. Among the 18 patients for whom epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) status was determined, 10 had sensitive EGFR mutations while 5 had ALK rearrangement; only 3 patients were driver gene mutation-negative. The 1-year overall survival (OS) rate was 62.31% and the 3- and 5-year survival rates were both 53.31%; median OS was not achieved (range, 3-86 months). Male sex, negative or unknown gene mutation status, stage IV, and squamous or small cell lung cancer were associated with poor prognosis (OS) in early-onset lung cancer. Conclusions: Lung cancer in young adults is distinctive, with adenocarcinoma and stage IV at presentation being predominant characteristics. Gene mutation assessment should be mandatory in this subgroup due to the increased likelihood of positive driver gene alterations, as individualized targeted therapy may achieve superior outcomes. Ivyspring International Publisher 2019-06-09 /pmc/articles/PMC6603399/ /pubmed/31293660 http://dx.doi.org/10.7150/jca.27490 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Liu, Bailong
Quan, Xiaoyue
Xu, Changgen
Lv, Jincai
Li, Cheng
Dong, Lihua
Liu, Min
Lung cancer in young adults aged 35 years or younger: A full-scale analysis and review
title Lung cancer in young adults aged 35 years or younger: A full-scale analysis and review
title_full Lung cancer in young adults aged 35 years or younger: A full-scale analysis and review
title_fullStr Lung cancer in young adults aged 35 years or younger: A full-scale analysis and review
title_full_unstemmed Lung cancer in young adults aged 35 years or younger: A full-scale analysis and review
title_short Lung cancer in young adults aged 35 years or younger: A full-scale analysis and review
title_sort lung cancer in young adults aged 35 years or younger: a full-scale analysis and review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6603399/
https://www.ncbi.nlm.nih.gov/pubmed/31293660
http://dx.doi.org/10.7150/jca.27490
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