Contouring variation affects estimates of normal tissue complication probability for breast fibrosis after radiotherapy
Jaikuna, T.; Osorio, E.V.; Azria, D.; Chang-Claude, J.; De Santis, M.C.; Gutiérrez-Enríquez, S.; van Herk, M.; Hoskin, P.; Lambrecht, M.; Lingard, Z.; Seibold, P.; Seoane, A.; Sperk, E.; Symonds, R.P.; Talbot, C.J.; Rancati, T.; Rattay, T.; Reyes, V.; Rosenstein, B.S.; de Ruysscher, D.; Vega Gliemmo, Ana; Veldeman, L.; Webb, A.; West, C.M.L.; Aznar, M.C.

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Identificadores
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Fecha de publicación
2023Título de revista
Breast
Tipo de contenido
Artigo
MeSH
Female | Humans | Radiotherapy Dosage | Breast Neoplasms | Breast | Radiotherapy Planning, Computer-Assisted | Probability | Fibrocystic Breast Disease | FibrosisResumen
Background: 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.
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