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NTCP modeling and dose–volume correlations for acute xerostomia and dry eye after whole brain radiation

BACKGROUND: Whole brain radiation (WBRT) may lead to acute xerostomia and dry eye from incidental parotid and lacrimal exposure, respectively. We performed a prospective observational study to assess the incidence/severity of this toxicity. We herein perform a secondary analysis relating parotid and...

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Autores principales: Mavroidis, Panayiotis, Pearlstein, Kevin A., Moon, Dominic H., Xu, Victoria, Royce, Trevor J., Weiner, Ashley A., Shen, Colette J., Marks, Lawrence B., Chera, Bhishamjit S., Das, Shiva K., Wang, Kyle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7981795/
https://www.ncbi.nlm.nih.gov/pubmed/33743773
http://dx.doi.org/10.1186/s13014-021-01786-6
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author Mavroidis, Panayiotis
Pearlstein, Kevin A.
Moon, Dominic H.
Xu, Victoria
Royce, Trevor J.
Weiner, Ashley A.
Shen, Colette J.
Marks, Lawrence B.
Chera, Bhishamjit S.
Das, Shiva K.
Wang, Kyle
author_facet Mavroidis, Panayiotis
Pearlstein, Kevin A.
Moon, Dominic H.
Xu, Victoria
Royce, Trevor J.
Weiner, Ashley A.
Shen, Colette J.
Marks, Lawrence B.
Chera, Bhishamjit S.
Das, Shiva K.
Wang, Kyle
author_sort Mavroidis, Panayiotis
collection PubMed
description BACKGROUND: Whole brain radiation (WBRT) may lead to acute xerostomia and dry eye from incidental parotid and lacrimal exposure, respectively. We performed a prospective observational study to assess the incidence/severity of this toxicity. We herein perform a secondary analysis relating parotid and lacrimal dosimetric parameters to normal tissue complication probability (NTCP) rates and associated models. METHODS: Patients received WBRT to 25–40 Gy in 10–20 fractions using 3D-conformal radiation therapy without prospective delineation of the parotids or lacrimals. Patients completed questionnaires at baseline and 1 month post-WBRT. Xerostomia was assessed using the University of Michigan xerostomia score (scored 0–100, toxicity defined as ≥ 20 pt increase) and xerostomia bother score (scored from 0 to 3, toxicity defined as ≥ 2 pt increase). Dry eye was assessed using the Subjective Evaluation of Symptom of Dryness (SESoD, scored from 0 to 4, toxicity defined as ≥ 2 pt increase). The clinical data were fitted by the Lyman–Kutcher–Burman (LKB) and Relative Seriality (RS) NTCP models. RESULTS: Of 55 evaluable patients, 19 (35%) had ≥ 20 point increase in xerostomia score, 11 (20%) had ≥ 2 point increase in xerostomia bother score, and 13 (24%) had ≥ 2 point increase in SESoD score. For xerostomia, parotid V(10Gy)–V(20Gy) correlated best with toxicity, with AUC 0.68 for xerostomia score and 0.69–0.71 for bother score. The values for the D(50), m and n parameters of the LKB model were 22.3 Gy, 0.84 and 1.0 for xerostomia score and 28.4 Gy, 0.55 and 1.0 for bother score, respectively. The corresponding values for the D(50), γ and s parameters of the RS model were 23.5 Gy, 0.28 and 0.0001 for xerostomia score and 32.0 Gy, 0.45 and 0.0001 for bother score, respectively. For dry eye, lacrimal V(10Gy)–V(15Gy) were found to correlate best with toxicity, with AUC values from 0.67 to 0.68. The parameter values of the LKB model were 53.5 Gy, 0.74 and 1.0, whereas of the RS model were 54.0 Gy, 0.37 and 0.0001, respectively. CONCLUSIONS: Xerostomia was most associated with parotid V(10Gy)–V(20Gy), and dry eye with lacrimal V(10Gy)–V(15Gy). NTCP models were successfully created for both toxicities and may help clinicians refine dosimetric goals and assess levels of risk in patients receiving palliative WBRT.
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spelling pubmed-79817952021-03-22 NTCP modeling and dose–volume correlations for acute xerostomia and dry eye after whole brain radiation Mavroidis, Panayiotis Pearlstein, Kevin A. Moon, Dominic H. Xu, Victoria Royce, Trevor J. Weiner, Ashley A. Shen, Colette J. Marks, Lawrence B. Chera, Bhishamjit S. Das, Shiva K. Wang, Kyle Radiat Oncol Research BACKGROUND: Whole brain radiation (WBRT) may lead to acute xerostomia and dry eye from incidental parotid and lacrimal exposure, respectively. We performed a prospective observational study to assess the incidence/severity of this toxicity. We herein perform a secondary analysis relating parotid and lacrimal dosimetric parameters to normal tissue complication probability (NTCP) rates and associated models. METHODS: Patients received WBRT to 25–40 Gy in 10–20 fractions using 3D-conformal radiation therapy without prospective delineation of the parotids or lacrimals. Patients completed questionnaires at baseline and 1 month post-WBRT. Xerostomia was assessed using the University of Michigan xerostomia score (scored 0–100, toxicity defined as ≥ 20 pt increase) and xerostomia bother score (scored from 0 to 3, toxicity defined as ≥ 2 pt increase). Dry eye was assessed using the Subjective Evaluation of Symptom of Dryness (SESoD, scored from 0 to 4, toxicity defined as ≥ 2 pt increase). The clinical data were fitted by the Lyman–Kutcher–Burman (LKB) and Relative Seriality (RS) NTCP models. RESULTS: Of 55 evaluable patients, 19 (35%) had ≥ 20 point increase in xerostomia score, 11 (20%) had ≥ 2 point increase in xerostomia bother score, and 13 (24%) had ≥ 2 point increase in SESoD score. For xerostomia, parotid V(10Gy)–V(20Gy) correlated best with toxicity, with AUC 0.68 for xerostomia score and 0.69–0.71 for bother score. The values for the D(50), m and n parameters of the LKB model were 22.3 Gy, 0.84 and 1.0 for xerostomia score and 28.4 Gy, 0.55 and 1.0 for bother score, respectively. The corresponding values for the D(50), γ and s parameters of the RS model were 23.5 Gy, 0.28 and 0.0001 for xerostomia score and 32.0 Gy, 0.45 and 0.0001 for bother score, respectively. For dry eye, lacrimal V(10Gy)–V(15Gy) were found to correlate best with toxicity, with AUC values from 0.67 to 0.68. The parameter values of the LKB model were 53.5 Gy, 0.74 and 1.0, whereas of the RS model were 54.0 Gy, 0.37 and 0.0001, respectively. CONCLUSIONS: Xerostomia was most associated with parotid V(10Gy)–V(20Gy), and dry eye with lacrimal V(10Gy)–V(15Gy). NTCP models were successfully created for both toxicities and may help clinicians refine dosimetric goals and assess levels of risk in patients receiving palliative WBRT. BioMed Central 2021-03-21 /pmc/articles/PMC7981795/ /pubmed/33743773 http://dx.doi.org/10.1186/s13014-021-01786-6 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Mavroidis, Panayiotis
Pearlstein, Kevin A.
Moon, Dominic H.
Xu, Victoria
Royce, Trevor J.
Weiner, Ashley A.
Shen, Colette J.
Marks, Lawrence B.
Chera, Bhishamjit S.
Das, Shiva K.
Wang, Kyle
NTCP modeling and dose–volume correlations for acute xerostomia and dry eye after whole brain radiation
title NTCP modeling and dose–volume correlations for acute xerostomia and dry eye after whole brain radiation
title_full NTCP modeling and dose–volume correlations for acute xerostomia and dry eye after whole brain radiation
title_fullStr NTCP modeling and dose–volume correlations for acute xerostomia and dry eye after whole brain radiation
title_full_unstemmed NTCP modeling and dose–volume correlations for acute xerostomia and dry eye after whole brain radiation
title_short NTCP modeling and dose–volume correlations for acute xerostomia and dry eye after whole brain radiation
title_sort ntcp modeling and dose–volume correlations for acute xerostomia and dry eye after whole brain radiation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7981795/
https://www.ncbi.nlm.nih.gov/pubmed/33743773
http://dx.doi.org/10.1186/s13014-021-01786-6
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