ICRU report 91 on prescribing, recording, and reporting of stereotactic treatments with small photon beams

Wilke, L.; Andratschke, Nicolaus; Blanck, Oliver; Brunner, Thomas; Combs, Stephanie E.; Grosu, Anca‐Ligia; Moustakis, Christos; Schmitt, Daniela; Baus, Wolfgang; Gückenberger, Matthias

doi:10.1007/s00066-018-1416-x

Cited by 156 publications

(135 citation statements)

References 23 publications

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“…Therefore, the D2% of the spinal cord shows significant value (P < 0.05). The dosimetric metrics of spinal cord PRV is more important in this study because the PRV is recommended for the structures of the nervous system including the spinal cord (11,19). Although the dose differences of the spinal cord, left lung, and bilateral lung are significant, their absolute difference is small and acceptable for clinical use.…”

Section: Discussionmentioning

confidence: 99%

Evaluation of Automatic Segmentation Model With Dosimetric Metrics for Radiotherapy of Esophageal Cancer

et al. 2020

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Results: Average DSC values were greater than 0.92 except for the spinal cord (0.82), and average MDA values were <0.90 mm except for the heart (1.74 mm). Eleven of the 20 dosimetric metrics of the OARs were not significant (P > 0.05). Although there were significant differences (P < 0.05) for the spinal cord (D2%), left lung (V10, V20, V30, and mean dose), and bilateral lung (V10, V20, V30, and mean dose), their absolute differences were small and acceptable for the clinic. The maximum dosimetric metrics differences of OARs between manual and automatic delineations were D2% = 0.35 Gy for the spinal cord and V30 = 0.4% for the bilateral lung, which were within the clinical criteria in this study. Conclusion: Dosimetric metrics were proposed to evaluate the automatic delineation in radiotherapy planning of esophageal cancer. Consequently, the automatic delineation could substitute the manual delineation for esophageal cancer radiotherapy planning based on the dosimetric evaluation in this study.

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Section: Discussionmentioning

confidence: 99%

Evaluation of Automatic Segmentation Model With Dosimetric Metrics for Radiotherapy of Esophageal Cancer

et al. 2020

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“…5. Prescribing, recording and reporting each SRS/FSRT/ SBRT treatment procedure according to international guidelines and standards is required (for further details see the International Commission on Radiation Units and Measurements report 91 on prescribing, recording, and reporting of stereotactic treatments with small photon beams and the statement of the DEGRO/DGMP working group stereotactic radiotherapy and radiosurgery [10])…”

Section: Process Quality Requirementsmentioning

confidence: 99%

Definition and quality requirements for stereotactic radiotherapy: consensus statement from the DEGRO/DGMP Working Group Stereotactic Radiotherapy and Radiosurgery

et al. 2020

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Stereotactic radiotherapy with its forms of intracranial stereotactic radiosurgery (SRS), intracranial fractionated stereotactic radiotherapy (FSRT) and stereotactic body radiotherapy (SBRT) is today a guideline-recommended treatment for malignant or benign tumors as well as neurological or vascular functional disorders. The working groups for radiosurgery and stereotactic radiotherapy of the German Society for Radiation Oncology (DEGRO) and for physics and technology in stereotactic radiotherapy of the German Society for Medical Physics (DGMP) have established a consensus statement about the definition and minimal quality requirements for stereotactic radiotherapy to achieve best clinical outcome and treatment quality in the implementation into routine clinical practice.

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“…For this first feasibility study, the treatment will be performed as an inpatient procedure or as outpatient produce with immediate inpatient submission after treatment. Cardiac radiosurgery will be prescribed, recorded, and reported on the basis of the International Commission on Radiation Units and Measurements (ICRU) report 91 for stereotactic treatments with small photon beams [69,70]. The essential data for CRT are the time-resolved non-contrast enhanced primary planning computed tomography (PCT), the contrast enhanced multi-phase ECG-gated cardiac CT (CCT), and electrophysiology mapping (EPM) data of the right or left ventricle.…”

Section: Study Treatmentmentioning

confidence: 99%

Radiosurgery for ventricular tachycardia: preclinical and clinical evidence and study design for a German multi-center multi-platform feasibility trial (RAVENTA)

et al. 2020

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Background Single-session high-dose stereotactic radiotherapy (radiosurgery) is a new treatment option for otherwise untreatable patients suffering from refractory ventricular tachycardia (VT). In the initial single-center case studies and feasibility trials, cardiac radiosurgery has led to significant reductions of VT burden with limited toxicities. However, the full safety profile remains largely unknown. Methods/design In this multi-center, multi-platform clinical feasibility trial which we plan is to assess the initial safety profile of radiosurgery for ventricular tachycardia (RAVENTA). High-precision image-guided single-session radiosurgery with 25 Gy will be delivered to the VT substrate determined by high-definition endocardial electrophysiological mapping. The primary endpoint is safety in terms of successful dose delivery without severe treatment-related side effects in the first Jürgen Dunst and Hendrik Bonnemeier have equally contributed to this work. This is the first publication for the RAVENTA study.

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ICRU report 91 on prescribing, recording, and reporting of stereotactic treatments with small photon beams

Cited by 156 publications

References 23 publications

Evaluation of Automatic Segmentation Model With Dosimetric Metrics for Radiotherapy of Esophageal Cancer

Evaluation of Automatic Segmentation Model With Dosimetric Metrics for Radiotherapy of Esophageal Cancer

Definition and quality requirements for stereotactic radiotherapy: consensus statement from the DEGRO/DGMP Working Group Stereotactic Radiotherapy and Radiosurgery

Radiosurgery for ventricular tachycardia: preclinical and clinical evidence and study design for a German multi-center multi-platform feasibility trial (RAVENTA)

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