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Comparison of diffusion-weighted MR imaging and FDG PET/CT to predict pathological complete response to neoadjuvant chemotherapy in patients with breast cancer

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dc.contributor.authorPark, Sang Hee-
dc.contributor.authorMoon, Woo Kyung-
dc.contributor.authorCho, Nariya-
dc.contributor.authorChang, Jung Min-
dc.contributor.authorIm, Seock-Ah-
dc.contributor.authorPark, In Ae-
dc.contributor.authorKang, Keon Wook-
dc.contributor.authorHan, Wonshik-
dc.contributor.authorNoh, Dong-Young-
dc.date.accessioned2022-03-22T09:09:27Z-
dc.date.available2022-03-22T09:09:27Z-
dc.date.created2018-05-24-
dc.date.created2018-05-24-
dc.date.created2018-05-24-
dc.date.created2018-05-24-
dc.date.issued2012-01-
dc.identifier.citationEuropean Radiology, Vol.22 No.1, pp.18-25-
dc.identifier.issn0938-7994-
dc.identifier.other36371-
dc.identifier.urihttps://hdl.handle.net/10371/177179-
dc.description.abstractTo compare the use of diffusion-weighted MR imaging (DWI) and (18)F-FDG PET/CT to predict pathological complete response (pCR) in breast cancer patients receiving neoadjuvant chemotherapy. Thirty-four women with 34 invasive breast cancers underwent DWI and PET/CT before and after chemotherapy and before surgery. The percentage changes in the apparent diffusion coefficient (ADC) and the standardised uptake value (SUV) were calculated, and the diagnostic performances for predicting pCR were evaluated using receiver operating characteristic (ROC) curve analysis. After surgery, 7/34 patients (20.6%) were found to have pCR. A (z) values for DWI, PET/CT and the combined use of DWI and PET/CT were 0.910, 0.873 and 0.944, respectively. The best cut-offs for differentiating pCR from non-pCR were a 54.9% increase in the ADC and a 63.9% decrease in the SUV. DWI showed 100% (7/7) sensitivity and 70.4% (19/27) specificity and PET/CT showed 100% sensitivity and 77.8% (21/27) specificity. When DWI and PET/CT were combined, there was a trend towards improved specificity compared with DWI. DWI and FDG PET/CT show similar diagnostic accuracy for predicting pCR to neoadjuvant chemotherapy in breast cancer patients. The combined use of DWI and FDG PET/CT has the potential to improve specificity in predicting pCR. Key Points aEuro cent DWI breast MR and PET/CT show similar accuracy for predicting pathological response aEuro cent The combined use of DWI and PET/CT can potentially improve specificity aEuro cent This can assist individualised treatment in breast cancer patients receiving neoadjvant chemotherapy.-
dc.language영어-
dc.publisherSpringer Verlag-
dc.titleComparison of diffusion-weighted MR imaging and FDG PET/CT to predict pathological complete response to neoadjuvant chemotherapy in patients with breast cancer-
dc.typeArticle-
dc.contributor.AlternativeAuthor임석아-
dc.identifier.doi10.1007/s00330-011-2236-x-
dc.citation.journaltitleEuropean Radiology-
dc.identifier.wosid000297749100003-
dc.identifier.scopusid2-s2.0-84857061446-
dc.citation.endpage25-
dc.citation.number1-
dc.citation.startpage18-
dc.citation.volume22-
dc.identifier.sci000297749100003-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorMoon, Woo Kyung-
dc.contributor.affiliatedAuthorCho, Nariya-
dc.contributor.affiliatedAuthorIm, Seock-Ah-
dc.contributor.affiliatedAuthorPark, In Ae-
dc.contributor.affiliatedAuthorKang, Keon Wook-
dc.contributor.affiliatedAuthorHan, Wonshik-
dc.contributor.affiliatedAuthorNoh, Dong-Young-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusPOSITRON-EMISSION-TOMOGRAPHY-
dc.subject.keywordPlusSURGICAL ADJUVANT BREAST-
dc.subject.keywordPlusPREOPERATIVE CHEMOTHERAPY-
dc.subject.keywordPlusTUMOR RESPONSE-
dc.subject.keywordPlusCOEFFICIENT-
dc.subject.keywordPlusCARCINOMA-
dc.subject.keywordPlusBIOMARKER-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusB-18-
dc.subject.keywordAuthorBreast cancer-
dc.subject.keywordAuthorChemotherapy-
dc.subject.keywordAuthorDiffusion-weighted imaging-
dc.subject.keywordAuthorFDG PET-
dc.subject.keywordAuthorPET/CT-
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  • College of Medicine
  • Department of Medicine
Research Area Clinical Medicine

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