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AI-Driven MRI Biomarkers for Breast Cancer Risk and Treatment Response Assessment
AI-Driven MRI Biomarkers for Breast Cancer Risk and Treatment Response Assessment
AI-Driven MRI Biomarkers for Breast Cancer Risk and Treatment Response Assessment

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20260202105150
ISBN  
9798293831098
DDC  
616
저자명  
Yan, Ran.
서명/저자  
AI-Driven MRI Biomarkers for Breast Cancer Risk and Treatment Response Assessment
발행사항  
[Sl] : University of California, Los Angeles, 2025
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2025
형태사항  
107 p
주기사항  
Source: Dissertations Abstracts International, Volume: 87-03, Section: A.
주기사항  
Advisor: Sung, Kyung H.;Wu, Holden H.
학위논문주기  
Thesis (Ph.D.)--University of California, Los Angeles, 2025.
초록/해제  
요약Breast cancer remains the most common malignancy in women worldwide, and quantitative biomarkers from breast MRI, including fibroglandular tissue (FGT) and background parenchymal enhancement (BPE), are emerging as important tools for risk assessment and treatment monitoring. To clarify the biological relevance of BPE, we analyzed screening MRI from 535 women stratified by lifetime risk and BRCA mutation status. After breast and FGT segmentation, six quantitative BPE measures were extracted, revealing strong associations with age, BMI, menopausal status, and breast density. Notably, BRCA1/2 carriers showed significantly lower enhancement than high-risk non-carriers after adjustment, suggesting a link between germline mutations and parenchymal physiology. Extending this work, we evaluated the predictive value of BPE for neoadjuvant chemotherapy (NAC) response in a multicenter cohort of 191 patients. Radiomics models combining tumor and BPE features achieved the best accuracy for predicting pathologic complete response, particularly in postmenopausal women and triple-negative cancers, highlighting the added value of BPE beyond tumor features alone. To enhance the reproducibility of breast MRI biomarkers, we developed an anatomy-aware loss function for deep learning-based FGT segmentation that integrates breast density information into the training process. Applied to 180 internal MRIs with independent evaluation on 40 held-out cases and an additional 100 external cases, this approach improved boundary accuracy and reduced biomarker estimation errors by approximately 10-15% compared with conventional loss functions, with the greatest benefit observed in fatty and scattered breasts. In conclusion, this work demonstrates that BPE is shaped by genetic and clinical risk factors, enhances prediction of treatment response, and can be more reliably quantified through anatomically informed segmentation, advancing its use as a robust imaging biomarker for breast cancer risk stratification and therapy monitoring.
일반주제명  
Medical imaging
일반주제명  
Oncology
일반주제명  
Womens studies
키워드  
Fibroglandular tissue
키워드  
Background parenchymal enhancement
키워드  
Neoadjuvant chemotherapy
기타저자  
University of California, Los Angeles Bioengineering 0288
기본자료저록  
Dissertations Abstracts International. 87-03A.
전자적 위치 및 접속  
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■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a616
■1001  ▼aYan,  Ran.
■24510▼aAI-Driven  MRI  Biomarkers  for  Breast  Cancer  Risk  and  Treatment  Response  Assessment
■260    ▼a[Sl]▼bUniversity  of  California,  Los  Angeles▼c2025
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
■300    ▼a107  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  87-03,  Section:  A.
■500    ▼aAdvisor:  Sung,  Kyung  H.;Wu,  Holden  H.
■5021  ▼aThesis  (Ph.D.)--University  of  California,  Los  Angeles,  2025.
■520    ▼aBreast  cancer  remains  the  most  common  malignancy  in  women  worldwide,  and  quantitative  biomarkers  from  breast  MRI,  including  fibroglandular  tissue  (FGT)  and  background  parenchymal  enhancement  (BPE),  are  emerging  as  important  tools  for  risk  assessment  and  treatment  monitoring.  To  clarify  the  biological  relevance  of  BPE,  we  analyzed  screening  MRI  from  535  women  stratified  by  lifetime  risk  and  BRCA  mutation  status.  After  breast  and  FGT  segmentation,  six  quantitative  BPE  measures  were  extracted,  revealing  strong  associations  with  age,  BMI,  menopausal  status,  and  breast  density.  Notably,  BRCA1/2  carriers  showed  significantly  lower  enhancement  than  high-risk  non-carriers  after  adjustment,  suggesting  a  link  between  germline  mutations  and  parenchymal  physiology.  Extending  this  work,  we  evaluated  the  predictive  value  of  BPE  for  neoadjuvant  chemotherapy  (NAC)  response  in  a  multicenter  cohort  of  191  patients.  Radiomics  models  combining  tumor  and  BPE  features  achieved  the  best  accuracy  for  predicting  pathologic  complete  response,  particularly  in  postmenopausal  women  and  triple-negative  cancers,  highlighting  the  added  value  of  BPE  beyond  tumor  features  alone.  To  enhance  the  reproducibility  of  breast  MRI  biomarkers,  we  developed  an  anatomy-aware  loss  function  for  deep  learning-based  FGT  segmentation  that  integrates  breast  density  information  into  the  training  process.  Applied  to  180  internal  MRIs  with  independent  evaluation  on  40  held-out  cases  and  an  additional  100  external  cases,  this  approach  improved  boundary  accuracy  and  reduced  biomarker  estimation  errors  by  approximately  10-15%  compared  with  conventional  loss  functions,  with  the  greatest  benefit  observed  in  fatty  and  scattered  breasts.  In  conclusion,  this  work  demonstrates  that  BPE  is  shaped  by  genetic  and  clinical  risk  factors,  enhances  prediction  of  treatment  response,  and  can  be  more  reliably  quantified  through  anatomically  informed  segmentation,  advancing  its  use  as  a  robust  imaging  biomarker  for  breast  cancer  risk  stratification  and  therapy  monitoring.
■590    ▼aSchool  code:  0031.
■650  4▼aMedical  imaging
■650  4▼aOncology
■650  4▼aWomens  studies
■653    ▼aFibroglandular  tissue
■653    ▼aBackground  parenchymal  enhancement
■653    ▼aNeoadjuvant  chemotherapy
■690    ▼a0574
■690    ▼a0453
■690    ▼a0992
■690    ▼a0769
■71020▼aUniversity  of  California,  Los  Angeles▼bBioengineering  0288.
■7730  ▼tDissertations  Abstracts  International▼g87-03A.
■790    ▼a0031
■791    ▼aPh.D.
■792    ▼a2025
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17359637▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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