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Träfflista för sökning "WFRF:(Pettersson Niclas 1974) srt2:(2020-2024)"

Sökning: WFRF:(Pettersson Niclas 1974) > (2020-2024)

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1.
  • Braide, Karin, et al. (författare)
  • Salvage radiation therapy in prostate cancer: relationship between rectal dose and long-term, self-reported rectal bleeding
  • 2021
  • Ingår i: Clinical & Translational Oncology. - : Springer Science and Business Media LLC. - 1699-048X .- 1699-3055. ; 23:2, s. 397-404
  • Tidskriftsartikel (refereegranskat)abstract
    • Purpose To quantify the relationship between the rectal dose distribution and the prevalence of self-reported rectal bleeding among men treated with salvage radiotherapy (ST) delivered by three-dimensional conformal radiotherapy (3DCRT) for prostate cancer. To use this relationship to estimate the risk of rectal bleeding for a contemporary cohort of patients treated with volumetric modulated arc therapy (VMAT) ST. Methods and patients Rectal bleeding of any grade was reported by 56 (22%) of 255 men in a PROM-survey at a median follow-up of 6.7 years after 3DCRT ST. Treatment plan data were extracted and dose-response relationships for the rectal volumes receiving at least 35 Gy (V-35Gy) or 63 Gy (V-63Gy) were calculated with logistic regression. These relationships were used to estimate the risk of rectal bleeding for a cohort of 253 patients treated with VMAT ST. Results In the dose-response analysis of patients in the 3DCRT ST cohort, both rectal V(35Gy)and V(63Gy)were statistically significant parameters in univariable analysis (p = 0.005 and 0.003, respectively). For the dose-response models using either rectal V(35Gy)or V-63Gy, the average calculated risk of rectal bleeding was 14% among men treated with VMAT ST compared to a reported prevalence of 22% for men treated with 3DCRT ST. Conclusions We identified dose-response relationships between the rectal dose distribution and the risk of self-reported rectal bleeding of any grade in a long-term perspective for men treated with 3DCRT ST. Furthermore, VMAT ST may have the potential to decrease the prevalence of late rectal bleeding.
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2.
  • Moiseenko, Vitali, et al. (författare)
  • A Primer on Dose-Response Data Modeling in Radiation Therapy.
  • 2021
  • Ingår i: International journal of radiation oncology, biology, physics. - : Elsevier BV. - 1879-355X .- 0360-3016. ; 110:1, s. 11-20
  • Tidskriftsartikel (refereegranskat)abstract
    • An overview of common approaches used to assess a dose response for radiation therapy-associated endpoints is presented, using lung toxicity data sets analyzed as a part of the High Dose per Fraction, Hypofractionated Treatment Effects in the Clinic effort as an example. Each component presented (eg, data-driven analysis, dose-response analysis, and calculating uncertainties on model prediction) is addressed using established approaches. Specifically, the maximum likelihood method was used to calculate best parameter values of the commonly used logistic model, the profile-likelihood to calculate confidence intervals on model parameters, and the likelihood ratio to determine whether the observed data fit is statistically significant. The bootstrap method was used to calculate confidence intervals for model predictions. Correlated behavior of model parameters and implication for interpreting dose response are discussed.
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3.
  • Mövik, Louise, 1993, et al. (författare)
  • Impact of delineation errors on the estimated organ at risk dose and of dose errors on the normal tissue complication probability model
  • 2023
  • Ingår i: Medical Physics. - : Wiley. - 0094-2405 .- 2473-4209. ; 50:3, s. 1879-1892
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Normal tissue complication probability (NTCP) models are often based on doses retrieved from delineated volumes. For retrospective dose-response studies focusing on organs that have not been delineated historically, automatic segmentation might be considered. However, automatic segmentation risks generating considerable delineation errors and knowledge regarding how these errors impact the estimated organ dose is important. Furthermore, organ-at-risk (OAR) dose uncertainties cannot be eliminated and might affect the resulting NTCP model. Therefore, it is also of interest to study how OAR dose errors impact the NTCP modeling results. Purpose: To investigate how random delineation errors of the proximal bronchial tree, heart, and esophagus impact the estimated OAR dose, and to investigate how random errors in the doses used for dose-response modeling affect the estimated NTCPs. Methods: We investigated the impact of random delineation errors on the estimated OAR dose using the treatment plans of 39 patients treated with conventionally fractionated radiation therapy of non-small-cell lung cancer. Study-specific reference structures were defined by manually contouring the proximal bronchial tree, heart and esophagus. For each patient and organ, 120 reshaped structures were created by introducing random shifts and margins to the entire reference structure. The mean and near-maximum dose to the reference and reshaped structures were compared. In a separate investigation, the impact of random dose errors on the NTCP model was studied performing dose-response modeling with study sets containing treatment outcomes and OAR doses with and without introduced errors. Universal patient populations with defined population risks, dose-response relationships and distributions of OAR doses were used as ground truth. From such a universal population, we randomly sampled data sets consisting of OAR dose and treatment outcome into reference populations. Study sets of different sizes were created by repeatedly introducing errors to the OAR doses of each reference population. The NTCP models generated with dose errors were compared to the reference NTCP model of the corresponding reference population. Results: A total of 14 040 reshaped structures with random delineation errors were created. The delineation errors resulted in systematic mean dose errors of less than 1% of the prescribed dose (PD). Mean dose differences above 15% of PD and near-maximum doses differences above 25% of PD were observed for 211 and 457 reshaped structures, respectively. Introducing random errors to OAR doses used for dose-response modeling resulted in systematic underestimations of the median NTCP. For all investigated scenarios, the median differences in NTCP were within 0.1 percentage points (p.p.) when comparing different study sizes. Conclusions: Introducing random delineation errors to the proximal bronchial tree, heart and esophagus resulted in mean dose and near-maximum dose differences above 15% and 25% of PD, respectively. We did not observe an association between the dose level and the magnitude of the dose errors. For the scenarios investigated in this study, introducing random errors to OAR doses used for dose-response modeling resulted in systematic underestimations of the median NTCP for reference risks higher than the universal population risk. The median NTCP underestimation was similar for different study sizes, all within 0.1 p.p.
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4.
  • Olsson, C. E., et al. (författare)
  • Feasibility of Mastication-Structure-Sparing Radiotherapy for Head and Neck Cancer
  • 2021
  • Ingår i: International journal of radiation oncology, biology, physics. - : Elsevier BV. - 1879-355X .- 0360-3016. ; 111:3
  • Tidskriftsartikel (refereegranskat)abstract
    • PURPOSE/OBJECTIVE(S): Although radiation-induced side-effects affecting mastication functionality have been studied in head and neck cancer (HNC) radiotherapy (RT), dose constraints for the associated structures are rarely included during treatment plan optimization. Previous research has identified several radiation dose relationships with mean dose thresholds around 30-40 Gy for masseter muscles, 40-50 Gy for pterygoid muscles, and 15-60 Gy for temporomandibular joint (TMJ) relating to a 10% trismus risk post RT. The purpose of this work was to use a multi-criteria optimization (MCO) approach to investigate to what extent doses to these structures can be lowered without violating existing clinical treatment goals in inverse planning of HNC RT. MATERIALS/METHODS: This exploratory treatment planning study used data from 22 HNC patients treated to 68 Gy without mastication-structure-sparing intent in 2017-2019 at one institute in Sweden. Original volumetric-modulated arc therapy (VMAT) plans were re-activated in the treatment planning system and masseter muscles, pterygoid muscles (medial and lateral), and TMJ were consistently delineated according to a previously reported delineation manual4. Re-planning was done using the MCO function of the treatment planning system with the resulting dose distribution normalized to match the clinical target volume (CTV T) mean dose of the clinical treatment plan. Dose differences between MCO and clinical plans were not allowed to exceed 2 Gy for any original clinical treatment goal unless tolerance doses had been substantially exceeded in the clinical treatment plan. To what extent dose to mastication structures could be lowered without violating existing clinical treatment goals were quantified by group and by patient. RESULTS: Altogether, there were 334 clinical treatment goals in the clinical treatment plans (median=15, range: 7-24 per patient, depending on tumor location), which easily could be met in the corresponding MCO plans. Mean doses to the mastication structures were in most cases below proposed tolerance doses in the clinical plan but could on average be further reduced between 3-5 Gy in the MCO plans (Table). Of the 25/88 patient reductions below 5 Gy (28%), 18/25 (72%) were for the masseter (n=8) and medial pterygoid (n=10) muscles. CONCLUSION: With modern RT, it seems possible to reduce the dose to mastication structures below proposed trismus dose tolerance thresholds for most HNC patients without violating clinical treatment goals. Focusing on masseter and medial pterygoid muscle doses may prove to give the largest benefit in individual cases. Copyright © 2021. Published by Elsevier Inc.
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5.
  • Pettersson, Niclas, 1974, et al. (författare)
  • Intrafractional relationship changes between an external breathing signal and fiducial marker positions in pancreatic cancer patients
  • 2020
  • Ingår i: Journal of Applied Clinical Medical Physics. - : Wiley. - 1526-9914. ; 21:3, s. 153-161
  • Tidskriftsartikel (refereegranskat)abstract
    • Background and purpose The purpose of this study of pancreatic cancer patients treated with respiratory-guided stereotactic body radiotherapy (SBRT) on a standard linac was to investigate (a) the intrafractional relationship change (IRC) between a breathing signal and the tumor position, (b) the impact of IRC on the delivered dose, and (c) potential IRC predictors. Materials and methods We retrospectively investigated 10 pancreatic cancer patients with 2-4 implanted fiducial markers in the tumor treated with SBRT. Fluoroscopic images were acquired before and after treatment delivery simultaneously with the abdominal breathing motion. We quantified the IRC as the change in fiducial location for a given breathing amplitude in the left-right (LR), anterior-posterior (AP), and superior-inferior (SI) directions from before to after treatment delivery. The treatment plans were re-calculated after changing the isocenter coordinates according to the IRCs. Four treatment- or patient-related factors were investigated as potential predictors for IRC using linear models. Results The average (+/- 1 SD) absolute IRCs in the LR, AP, and SI directions were 1.2 +/- 1.2 mm, 0.7 +/- 0.7 mm, and 1.1 +/- 0.8 mm, respectively. The average 3D IRC was 2.0 +/- 1.3 mm (range: 0.4-5.3 mm) for a median treatment delivery time of 8.5 min (range: 5.7-19.9 min; n = 31 fractions). The dose coverage of the internal target volume (ITV) decreased by more than 3% points in three of 31 fractions. In those cases, the 3D IRC had been larger than 4.3 mm. The 3D IRC was found to correlate with changes in the minimum breathing amplitude during treatment delivery. Conclusion On average, 2 mm of treatment delivery accuracy was lost due to IRC. Periodical intrafractional imaging is needed to safely deliver respiratory-guided SBRT.
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6.
  • Polymeri, Erini, et al. (författare)
  • Artificial Intelligence-Based Organ Delineation for Radiation Treatment Planning of Prostate Cancer on Computed Tomography
  • 2024
  • Ingår i: Advances in Radiation Oncology. - 2452-1094. ; 9:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Purpose: Meticulous manual delineations of the prostate and the surrounding organs at risk are necessary for prostate cancer radiation therapy to avoid side effects to the latter. This process is time consuming and hampered by inter- and intraobserver variability, all of which could be alleviated by artificial intelligence (AI). This study aimed to evaluate the performance of AI compared with manual organ delineations on computed tomography (CT) scans for radiation treatment planning. Methods and Materials: Manual delineations of the prostate, urinary bladder, and rectum of 1530 patients with prostate cancer who received curative radiation therapy from 2006 to 2018 were included. Approximately 50% of those CT scans were used as a training set, 25% as a validation set, and 25% as a test set. Patients with hip prostheses were excluded because of metal artifacts. After training and fine-tuning with the validation set, automated delineations of the prostate and organs at risk were obtained for the test set. Sørensen-Dice similarity coefficient, mean surface distance, and Hausdorff distance were used to evaluate the agreement between the manual and automated delineations. Results: The median Sørensen-Dice similarity coefficient between the manual and AI delineations was 0.82, 0.95, and 0.88 for the prostate, urinary bladder, and rectum, respectively. The median mean surface distance and Hausdorff distance were 1.7 and 9.2 mm for the prostate, 0.7 and 6.7 mm for the urinary bladder, and 1.1 and 13.5 mm for the rectum, respectively. Conclusions: Automated CT-based organ delineation for prostate cancer radiation treatment planning is feasible and shows good agreement with manually performed contouring.
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