Contouring variation affects estimates of normal tissue complication probability for breast fibrosis after radiotherapy

dc.contributor.authorJaikuna T.
dc.contributor.authorOsorio E.V.
dc.contributor.authorAzria D.
dc.contributor.authorChang-Claude J.
dc.contributor.authorDe Santis M.C.
dc.contributor.authorGutiérrez-Enríquez S.
dc.contributor.authorvan Herk M.
dc.contributor.authorHoskin P.
dc.contributor.authorLambrecht M.
dc.contributor.authorLingard Z.
dc.contributor.authorSeibold P.
dc.contributor.authorSeoane A.
dc.contributor.authorSperk E.
dc.contributor.authorSymonds R.P.
dc.contributor.authorTalbot C.J.
dc.contributor.authorRancati T.
dc.contributor.authorRattay T.
dc.contributor.authorReyes V.
dc.contributor.authorRosenstein B.S.
dc.contributor.authorde Ruysscher D.
dc.contributor.authorVega A.
dc.contributor.authorVeldeman L.
dc.contributor.authorWebb A.
dc.contributor.authorWest C.M.L.
dc.contributor.authorAznar M.C.
dc.contributor.otherMahidol University
dc.date.accessioned2023-09-21T18:01:03Z
dc.date.available2023-09-21T18:01:03Z
dc.date.issued2023-12-01
dc.description.abstractBackground: Normal tissue complication probability (NTCP) models can be useful to estimate the risk of fibrosis after breast-conserving surgery (BCS) and radiotherapy (RT) to the breast. However, they are subject to uncertainties. We present the impact of contouring variation on the prediction of fibrosis. Materials and methods: 280 breast cancer patients treated BCS-RT were included. Nine Clinical Target Volume (CTV) contours were created for each patient: i) CTV_crop (reference), cropped 5 mm from the skin and ii) CTV_skin, uncropped and including the skin, iii) segmenting the 95% isodose (Iso95%) and iv) 3 different auto-contouring atlases generating uncropped and cropped contours (Atlas_skin/Atlas_crop). To illustrate the impact of contour variation on NTCP estimates, we applied two equations predicting fibrosis grade ≥ 2 at 5 years, based on Lyman-Kutcher-Burman (LKB) and Relative Seriality (RS) models, respectively, to each contour. Differences were evaluated using repeated-measures ANOVA. For completeness, the association between observed fibrosis events and NTCP estimates was also evaluated using logistic regression. Results: There were minimal differences between contours when the same contouring approach was followed (cropped and uncropped). CTV_skin and Atlas_skin contours had lower NTCP estimates (−3.92%, IQR 4.00, p < 0.05) compared to CTV_crop. No significant difference was observed for Atlas_crop and Iso95% contours compared to CTV_crop. For the whole cohort, NTCP estimates varied between 5.3% and 49.5% (LKB) or 2.2% and 49.6% (RS) depending on the choice of contours. NTCP estimates for individual patients varied by up to a factor of 4. Estimates from “skin” contours showed higher agreement with observed events. Conclusion: Contour variations can lead to significantly different NTCP estimates for breast fibrosis, highlighting the importance of standardising breast contours before developing and/or applying NTCP models.
dc.identifier.citationBreast Vol.72 (2023)
dc.identifier.doi10.1016/j.breast.2023.103578
dc.identifier.eissn15323080
dc.identifier.issn09609776
dc.identifier.scopus2-s2.0-85170699959
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/90075
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.titleContouring variation affects estimates of normal tissue complication probability for breast fibrosis after radiotherapy
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85170699959&origin=inward
oaire.citation.titleBreast
oaire.citation.volume72
oairecerif.author.affiliationInstituto de Investigación Sanitaria de Santiago de Compostela
oairecerif.author.affiliationMedizinische Fakultät Mannheim
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationCollege of Life Sciences
oairecerif.author.affiliationVall d‘Hebron Institut de Oncologia
oairecerif.author.affiliationUniversité de Montpellier
oairecerif.author.affiliationCentro de Investigación Biomédica en Red de Enfermedades Raras
oairecerif.author.affiliationUniversitair Ziekenhuis Gent
oairecerif.author.affiliationUniversity of Leicester
oairecerif.author.affiliationKU Leuven
oairecerif.author.affiliationGerman Cancer Research Center
oairecerif.author.affiliationSchool of Medical Sciences
oairecerif.author.affiliationIcahn School of Medicine at Mount Sinai
oairecerif.author.affiliationHospital Universitari Vall d'Hebron
oairecerif.author.affiliationMaastricht Universitair Medisch Centrum+
oairecerif.author.affiliationFondazione IRCCS Istituto Nazionale dei Tumori, Milan
oairecerif.author.affiliationUniversitätsklinikum Hamburg-Eppendorf
oairecerif.author.affiliationFondazione IRCCS Nazionale dei Tumori
oairecerif.author.affiliationGrupo de Medicina Xenómica (USC)

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