3 351

Cited 37 times in

Personalized therapy on the horizon for squamous cell carcinoma of the lung

Authors
 Han Sang Kim  ;  Tetsuya Mitsudomi  ;  Ross A. Soo  ;  Byoung Chul Cho 
Citation
 LUNG CANCER, Vol.80(3) : 249-255, 2013 
Journal Title
LUNG CANCER
ISSN
 0169-5002 
Issue Date
2013
MeSH
Adenocarcinoma/genetics ; Adenocarcinoma/pathology ; Carcinoma, Non-Small-Cell Lung/genetics ; Carcinoma, Non-Small-Cell Lung/pathology ; Carcinoma, Squamous Cell/genetics* ; Carcinoma, Squamous Cell/pathology ; Clinical Trials as Topic ; Humans ; Lung Neoplasms/genetics* ; Lung Neoplasms/pathology ; Molecular Targeted Therapy* ; Mutation ; Precision Medicine*
Keywords
Squamous cell carcinoma ; Non-small cell lung cancer ; Targeted therapy ; Driver mutation ; Biomarker
Abstract
Squamous cell carcinoma (SQCC) of the lung is the second-largest subtype of non-small cell lung cancer (NSCLC), causing an estimated 400,000 deaths per year worldwide. Recent developments in cancer genome sequencing technology expanded our knowledge of driver mutations, which were identified as novel candidates for targeted therapy in various cancers. Successful targeted treatments for lung adenocarcinoma, NSCLC's primary subtype, with EGFR mutation or ALK fusion are clinically available, and a clinical trial of personalized targeted therapy in patients with lung adenocarcinoma is underway by the Lung Cancer Mutation Consortium. Although there are targeted treatments for lung adenocarcinoma, no personalized therapies currently exist for SQCC. Recently, comprehensive genomic characterization of lung SQCC using massively parallel sequencing has enabled us to identify several potential driver mutations/signaling pathways. These are FGFR1 amplifications, PI3KCA mutations, PTEN mutations/deletions, PDGFRA amplifications/mutations, and DDR2 mutations. The march toward personalized therapy may have taken a step forward with the discovery of these potential biomarkers for the treatment of SQCC of the lung.

This article reviewed the current knowledge of genomic landscape of lung SQCC and summarized ongoing clinical trials of targeted agents for lung SQCC. Also, we will suggest several other actionable mutations with matching drugs that should be investigated in future clinical trials for the personalized treatment of lung SQCC.
Full Text
http://www.sciencedirect.com/science/article/pii/S0169500213000743
DOI
10.1016/j.lungcan.2013.02.015
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Han Sang(김한상) ORCID logo https://orcid.org/0000-0002-6504-9927
Cho, Byoung Chul(조병철) ORCID logo https://orcid.org/0000-0002-5562-270X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/87891
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse

Links