5 results on '"Sijtsema, Nienke D."'
Search Results
2. Accounting for fractionation and heterogeneous dose distributions in the modelling of osteoradionecrosis in oropharyngeal carcinoma treatment.
- Author
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Verduijn GM, Sijtsema ND, van Norden Y, Heemsbergen WD, Mast H, Sewnaik A, Chin D, Baker S, Capala ME, van der Lugt A, van Meerten E, Hoogeman MS, and Petit SF
- Subjects
- Humans, Retrospective Studies, Male, Female, Middle Aged, Aged, Radiosurgery adverse effects, Radiosurgery methods, Aged, 80 and over, Adult, Risk Factors, Radiotherapy Dosage, Carcinoma, Squamous Cell radiotherapy, Radiation Dose Hypofractionation, Osteoradionecrosis etiology, Oropharyngeal Neoplasms radiotherapy, Dose Fractionation, Radiation, Radiotherapy, Intensity-Modulated adverse effects, Radiotherapy, Intensity-Modulated methods
- Abstract
Background and Purpose: Osteoradionecrosis (ORN) of the mandible is a severe complication following radiotherapy (RT). With a renewed interest in hypofractionation for head and neck radiotherapy, more information concerning ORN development after high fraction doses is important. The aim of this explorative study was to develop a model for ORN risk prediction applicable across different fractionation schemes using Equivalent Uniform Doses (EUD)., Material and Methods: We performed a retrospective cohort study in 334 oropharyngeal squamous cell carcinoma (OPSCC) patients treated with either a hypofractionated Stereotactic Body Radiation Therapy (HF-SBRT) boost or conventional Intensity Modulated Radiation Therapy (IMRT). ORN was scored with the CTCAE v5.0. HF-SBRT and IMRT dose distributions were converted into equivalent dose in 2 Gy fractions (α/β = 0.85 Gy) and analyzed using EUD. The parameter a that led to an EUD that best discriminated patients with and without grade ≥ 2 ORN was selected. Patient and treatment-related risk factors of ORN were analyzed with uni- and multivariable regression analysis., Results: A total of 32 patients (9.6%) developed ORN grade ≥ 2. An EUD(a = 8) best discriminated between ORN and non-ORN (AUC = 0.71). In multivariable regression, pre-RT extractions (SHR = 2.34; p = 0.012), mandibular volume (SHR = 1.04; p = 0.003), and the EUD(a = 8) (SHR = 1.14; p < 0.001) were significantly associated with ORN., Conclusion: Risk models for ORN based on conventional DVH parameters cannot be directly applied to HF-SBRT fractionation schemes and dose distributions. However, after correcting for fractionation and non-uniform dose distributions using EUD, a single model can distinguish between ORN and non-ORN after conventionally fractionated radiotherapy and hypofractionated boost treatments., Competing Interests: Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: [The department of radiotherapy has research collaborations with Elekta AB, Stockholm, Sweden, Accuray Inc., Sunnyvale, CA, USA, and Varian, Palo Alto, CA, USA and has received a research grant from the Dutch Cancer Society.]., (Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.)
- Published
- 2023
- Full Text
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3. Development of a local dose-response relationship for osteoradionecrosis within the mandible.
- Author
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Sijtsema ND, Verduijn GM, Nasserinejad K, van Norden Y, Mast H, van der Lugt A, Hoogeman MS, and Petit SF
- Subjects
- Humans, Radiotherapy Dosage, Smoking, Mandible, Retrospective Studies, Osteoradionecrosis etiology, Oropharyngeal Neoplasms radiotherapy, Head and Neck Neoplasms radiotherapy
- Abstract
Purpose: Osteoradionecrosis (ORN) of the mandible is a severe complication following radiotherapy of the head and neck, but not all regions of the mandible may be equally at risk. Therefore our goal was to explore a local dose response relationship for subregions of the mandible., Materials and Methods: All oropharyngeal cancer patients treated at our hospital between 2009 and 2016 were reviewed. Follow-up was cut-off at 3 years. For patients that developed ORN, the ORN volume was delineated on the planning CT. Each mandible was divided into 16 volumes of interest (VOIs) based on the location of the dental elements and the presence of ORN in each was scored. Generalized estimating equations were used to build a model for the probability of developing ORN in an element VOI., Results: Of the 219 included patients, 22 developed ORN in 89 element VOIs. Mean dose to the element VOI (odds ratio (OR) = 1.05 per Gy, 95% confidence interval (CI): (1.04,1.07)), pre-radiotherapy extractions of an element ipsilateral to element of interest (OR = 2.81, 95% CI: (1.12,7.05)), and smoking at start of radiotherapy (OR = 3.37, 95% CI: (1.29,8.78)) were significantly associated with an increased probability of ORN in the VOI., Conclusion: The developed dose-response model indicates that the probability of ORN varies within the mandible and strongly depends on the local dose, the location of extractions, and smoking., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2023
- Full Text
- View/download PDF
4. Osteoradionecrosis after postoperative radiotherapy for oral cavity cancer: A retrospective cohort study.
- Author
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Möring MM, Mast H, Wolvius EB, Verduijn GM, Petit SF, Sijtsema ND, Jonker BP, Nout RA, and Heemsbergen WD
- Subjects
- Cohort Studies, Humans, Radiotherapy Dosage, Retrospective Studies, Head and Neck Neoplasms complications, Mandibular Diseases complications, Mandibular Diseases epidemiology, Mouth Neoplasms complications, Mouth Neoplasms radiotherapy, Mouth Neoplasms surgery, Osteoradionecrosis epidemiology, Osteoradionecrosis etiology
- Abstract
Objective: Osteoradionecrosis (ORN) is a severe late complication after radiotherapy but current knowledge on ORN risks in the setting of postoperative radiotherapy (PORT) is limited. We studied the incidence and risk factors of ORN in patients with oral cavity cancers (OCC, treated with PORT., Patients and Methods: A retrospective cohort study was conducted including OCC patients (mainly squamous cell) treated with postoperative intensity modulated radiotherapy between 2010 and 2018 with > 1 year disease-free survival. Cumulative incidences of ORN were computed using the Kaplan Meier method. Clinical and dosimetric risk factors for mandibular ORN were evaluated using Cox regression models., Results: Within our cohort (N = 227, median follow-up 49 months) we observed 46 cases of ORN, mainly in the mandible (n = 41). The cumulative incidence of mandibular ORN was 15.9 % (SE 2.5 %) at three years and 19.8 % (SE 3.0 %) at five years. At univariable analysis, smoking, mandibular mandibulotomy or segment resection, mean dose to the mandible, and mandible volume (%) ≥ 60 Gy (V60) were significantly associated with increased ORN risks. At multivariable analysis, smoking (HR 2.13, 95 %CI 1.12-4.06) and V60 (HR 1.02 per 1 % increase, 95 %CI 1.01-1.04) remained predictive factors. For active smokers with a high V60 ≥ 40 % we observed rapid ORN development with a 1-year incidence of 29 % vs 6 % for others (p < 0.01)., Conclusion: OCC Patients treated with PORT are at high risk for mandibular ORN. We identified the mandibular volume receiving ≥ 60 Gy as the dominant risk factor, especially in active smokers. Limiting high-dose volumes at treatment planning may decrease ORN risks., (Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2022
- Full Text
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5. P-64 Incidence and risk factors of osteoradionecrosis of the mandible after modern radiotherapy for oropharyngeal carcinoma.
- Author
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Verduijn, Gerda M., Sijtsema, Nienke D., van Norden, Yvette, Heemsbergen, Wilma D., Mast, Hetty, Sewnaik, Aniel, Hove, Ivo ten, Chin, Denzel, Baker, Sarah, van der Lugt, Aad, Hoogeman, Mischa S., and Petit, Steven
- Subjects
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MANDIBLE , *CARCINOMA , *RADIOTHERAPY , *OSTEORADIONECROSIS - Published
- 2021
- Full Text
- View/download PDF
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