0 9

Cited 0 times in

Cited 0 times in

Deep Learning-Based Synthetic Contrast-Enhanced Breast MRI for Monitoring Response to Neoadjuvant Therapy

DC Field Value Language
dc.contributor.authorSujichantararat, Suleeporn-
dc.contributor.authorBiswas, Debosmita-
dc.contributor.authorKazerouni, Anum S.-
dc.contributor.authorTsang, Edric D.-
dc.contributor.authorSathe, Aditi-
dc.contributor.authorHippe, Daniel S.-
dc.contributor.authorPark, Vivian Y.-
dc.contributor.authorChung, Maggie-
dc.contributor.authorSpecht, Jennifer M.-
dc.contributor.authorDintzis, Suzanne M.-
dc.contributor.authorRahbar, Habib-
dc.contributor.authorHolmes, James H.-
dc.contributor.authorHuang, Wei-
dc.contributor.authorPartridge, Savannah C.-
dc.date.accessioned2026-07-10T07:43:52Z-
dc.date.available2026-07-10T07:43:52Z-
dc.date.created2026-07-07-
dc.date.issued2026-06-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/212921-
dc.description.abstractBackground/Objectives: Contrast-enhanced (CE) breast MRI is highly sensitive for evaluating breast cancer extent and response to neoadjuvant therapy (NAT) but requires intravenous administration of gadolinium-based contrast agents (GBCA), increasing cost, time, patient discomfort, and health concerns. This study explored the feasibility of reducing GBCA use in treatment monitoring using a deep learning (DL) model to synthesize CE-MRI from non-contrast MRI. Methods: This IRB-approved retrospective pilot study evaluated women with breast cancer enrolled in an ongoing trial using serial MRI to monitor NAT prior to surgery. A pre-trained DL model was used to synthesize CE-MRI from T1-, T2-, and diffusion-weighted MRI. Changes in tumor volume at early (post-1-cycle NAT) and mid-treatment were measured on synthetic and acquired CE-MRI. Performance for predicting residual cancer burden (RCB) class 0/1 was evaluated using AUC and compared with DeLong&apos;s test. Results: 27 women were included in the study (median age, 47 years [range = 28-75]); 14 (52%) achieved RCB class 0 and six (22%) achieved class 1. Synthetic CE-MRI-derived tumor volumes showed strong correlation with those from acquired CE-MRI at pre-treatment (rho = 0.92, p < 0.001) and early treatment (rho = 0.83, p < 0.001), but lower agreement at mid-treatment (rho = 0.57, p = 0.002). Change in tumor volume on synthetic CE-MRI was numerically similar to acquired CE-MRI for predicting RCB class 0/1 vs. 2/3 at both early (AUC = 0.84 vs. 0.86, p = 0.83) and mid-treatment (AUC = 0.73 vs. 0.75, p = 0.80). Conclusions: Synthetic CE-MRI demonstrates preliminary feasibility as a non-contrast surrogate for predicting favorable outcomes (RCB class 0/1) in this pilot study, but inconsistencies in tumor volume measurement vs. acquired CE-MRI warrant further model refinement and validation.-
dc.languageEnglish-
dc.publisherMDPI-
dc.relation.isPartOfCANCERS-
dc.relation.isPartOfCANCERS-
dc.titleDeep Learning-Based Synthetic Contrast-Enhanced Breast MRI for Monitoring Response to Neoadjuvant Therapy-
dc.typeArticle-
dc.contributor.googleauthorSujichantararat, Suleeporn-
dc.contributor.googleauthorBiswas, Debosmita-
dc.contributor.googleauthorKazerouni, Anum S.-
dc.contributor.googleauthorTsang, Edric D.-
dc.contributor.googleauthorSathe, Aditi-
dc.contributor.googleauthorHippe, Daniel S.-
dc.contributor.googleauthorPark, Vivian Y.-
dc.contributor.googleauthorChung, Maggie-
dc.contributor.googleauthorSpecht, Jennifer M.-
dc.contributor.googleauthorDintzis, Suzanne M.-
dc.contributor.googleauthorRahbar, Habib-
dc.contributor.googleauthorHolmes, James H.-
dc.contributor.googleauthorHuang, Wei-
dc.contributor.googleauthorPartridge, Savannah C.-
dc.identifier.doi10.3390/cancers18111835-
dc.relation.journalcodeJ03449-
dc.identifier.eissn2072-6694-
dc.identifier.pmid42279418-
dc.subject.keywordbreast-
dc.subject.keywordcancer-
dc.subject.keywordgadolinium-
dc.subject.keywordtreatment response-
dc.subject.keywordMRI-
dc.subject.keywordneoadjuvant therapy (NAT)-
dc.subject.keywordresidual cancer burden (RCB)-
dc.subject.keywordpathologic complete response (pCR)-
dc.subject.keywordsynthetic contrast-enhanced MRI modeling-
dc.contributor.affiliatedAuthorPark, Vivian Y.-
dc.identifier.scopusid2-s2.0-105041454165-
dc.identifier.wosid001789987100001-
dc.citation.volume18-
dc.citation.number11-
dc.identifier.bibliographicCitationCANCERS, Vol.18(11), 2026-06-
dc.identifier.rimsid94555-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorbreast-
dc.subject.keywordAuthorcancer-
dc.subject.keywordAuthorgadolinium-
dc.subject.keywordAuthortreatment response-
dc.subject.keywordAuthorMRI-
dc.subject.keywordAuthorneoadjuvant therapy (NAT)-
dc.subject.keywordAuthorresidual cancer burden (RCB)-
dc.subject.keywordAuthorpathologic complete response (pCR)-
dc.subject.keywordAuthorsynthetic contrast-enhanced MRI modeling-
dc.subject.keywordPlusFREE SURVIVAL-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalResearchAreaOncology-
dc.identifier.articleno1835-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers

qrcode

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