Repository logo
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
Repository logo
    Communities & Collections
    Research Outputs
    Fundings & Projects
    People
    Organizations
    Statistics
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
  1. Home
  2. .TMU Publications / 北醫出版品(教師升等著作 / 教學實踐 / 學位論文)
  3. .博碩士學位論文
  4. 103學年度
  5. 肺腺癌中上皮細胞生長因子受體突變與肺部腫瘤放射線治療後療效關聯性探討
 
  • Details
Options

肺腺癌中上皮細胞生長因子受體突變與肺部腫瘤放射線治療後療效關聯性探討

Other Title
Double Epidermal Growth Factor Receptor Mutations Is Associated With Better Clinical Outcomes After Thoracic Radiotherapy In Patients With Lung Adenocarcinoma
Type
thesis
Date Issued
2015-06-24
Author(s)
李明憲
Advisor
許明暉
Subjects
系所名稱:醫學資訊研究所
Description
學位別:碩士
語文別:中文
指導教授:許明暉
共同指導教授:
口試委員:蔡若婷;邱泓文
中文關鍵字:肺腺癌;放射線治療;上皮細胞生長因子受體突變
英文關鍵字:lung adenocarcinoma;radiotherapy;epidermal growth factor receptor mutation
Abstract
目的:分析肺腺癌患者,希望能從目前已知的分子生物標記中找出擁有哪些標記的肺腺癌細胞對於放射線治療有較佳的反應。

研究方法:收集從西元2010年1月到2013年12月到放射腫瘤科接受肺部放射線治療的肺腺癌患者,共有48位進入研究分析。運用線性迴歸以及決策樹模式分析相關臨床因子與「殘餘腫瘤負擔」的相關性。運用 Cox 比例風險模型分析相關臨床因子與存活率的相關性。

研究結果:從研究分析發現上皮細胞生長因子受體基因突變與「殘餘腫瘤負擔」明顯的相關性。有基因突變的患者比較常見是在女性非抽煙族群。18位基因突變的患者只有單一基因序列突變的有15(83.3%)位,同時有二處基因序列突變的有3(16.7)位。平均「殘餘腫瘤負擔」在基因突變的患者為56.7%在沒有基因突變的患者為55.4%。平均「殘餘腫瘤負擔」在同時有二處基因突變的患者為19.9%在只有單一基因突變的患者為64.0%。在單變數分析發現基因序列 18、20、21以及同時二處序列突變對於「殘餘腫瘤負擔」是明顯相關因子。基因突變的患者對比於沒有突變的患者似乎有比較長的存活期但沒有統計上的明顯差異(31.1 vs. 26.6 months; P=0.49)。存活期中位數在同時二處基因突變的患者以及沒有基因突變的患者分別是 20.1 個月以及16.9個月。

結論:從研究分析發現上皮細胞生長因子受體基因突變與「殘餘腫瘤負擔」明顯的相關性。同時二處基因序列突變對於「殘餘腫瘤負擔」有更明顯的效果,並且可能有比較長的存活期。
URI
https://203.71.86.71/handle/123456789/57223

Copyright Notice

● The digital content on this platform is part of the Taipei Medical University Institutional Repository, featuring various academic works and outputs from the institution. It offers free access to academic research and public education for non-commercial use.

● Please use the content appropriately and within legal boundaries to respect copyright owners' rights. For commercial use, please obtain prior authorization from the copyright owner. Users must not use TMUIR for any illegal purposes.

● By utilising the platform, users are deemed to have fully accepted and understood all the regulations set out in this statement, relevant laws of the Republic of China, all international internet regulations, and usage conventions.

● TMUIR is committed to protecting the interests of copyright owners. If you believe that any material on this website infringes copyright, please contact our staff at libirtmu@gmail.com, and we will remove the work from the repository.

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science

  • Cookie settings
  • Privacy policy
  • End User Agreement
  • Send Feedback