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      Wait-and-scan management in sporadic Koos grade 4 vestibular schwannomas: A longitudinal volumetric study

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          Abstract

          Background

          Volumetric natural history studies specifically on large vestibular schwannomas (VSs), commonly classified as Koos grade 4, are lacking. The aim of the current study is to present the volumetric tumor evolution in sporadic Koos grade 4 VSs and possible predictors for tumor growth.

          Methods

          Volumetric tumor measurements and tumor evolution patterns from serial MRI studies were analyzed from selected consecutive patients with Koos grade 4 VS undergoing initial wait-and-scan management between January 2001 and July 2020. The significant volumetric threshold was defined as a change in volume of ≥10%.

          Results

          Among 215 tumors with a median size (IQR) of 2.7 cm 3 (1.8–4.2), 147 tumors (68%) demonstrated growth and 75 tumors (35%) demonstrated shrinkage during follow-up. Growth-free survival rates (95% CI) at 1, 2, 5, and 10 years were 55% (48–61), 36% (29–42), 29% (23–36), and 28% (21–34), respectively and did not significantly differ in tumors> 20 mm (Chi-square = .40; P-value = .53). Four tumor evolution patterns (% of total) were observed: continued growth (60); initial growth then shrinkage (7); continued shrinkage (27); and stability (5). Good hearing (adjusted HR 2.21, 95% CI 1.48–3.30; P < .001) and peritumoral edema (adjusted HR 2.22, 95% CI 1.18–4.13; P = .01) at diagnosis were significantly associated with an increased likelihood of growth.

          Conclusions

          Koos grade 4 VSs show a wide variety in size and growth. Due to variable growth patterns, an initial wait-and-scan strategy with short scan intervals may be an acceptable option in selected tumors, if no significant clinical symptoms of mass effect that warrant treatment are present.

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          Most cited references37

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          User-guided 3D active contour segmentation of anatomical structures: significantly improved efficiency and reliability.

          Active contour segmentation and its robust implementation using level set methods are well-established theoretical approaches that have been studied thoroughly in the image analysis literature. Despite the existence of these powerful segmentation methods, the needs of clinical research continue to be fulfilled, to a large extent, using slice-by-slice manual tracing. To bridge the gap between methodological advances and clinical routine, we developed an open source application called ITK-SNAP, which is intended to make level set segmentation easily accessible to a wide range of users, including those with little or no mathematical expertise. This paper describes the methods and software engineering philosophy behind this new tool and provides the results of validation experiments performed in the context of an ongoing child autism neuroimaging study. The validation establishes SNAP intrarater and interrater reliability and overlap error statistics for the caudate nucleus and finds that SNAP is a highly reliable and efficient alternative to manual tracing. Analogous results for lateral ventricle segmentation are provided.
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            EANO guideline on the diagnosis and treatment of vestibular schwannoma

            The level of evidence to provide treatment recommendations for vestibular schwannoma is low compared with other intracranial neoplasms. Therefore, the vestibular schwannoma task force of the European Association of Neuro-Oncology assessed the data available in the literature and composed a set of recommendations for health care professionals. The radiological diagnosis of vestibular schwannoma is made by magnetic resonance imaging. Histological verification of the diagnosis is not always required. Current treatment options include observation, surgical resection, fractionated radiotherapy, and radiosurgery. The choice of treatment depends on clinical presentation, tumor size, and expertise of the treating center. In small tumors, observation has to be weighed against radiosurgery, in large tumors surgical decompression is mandatory, potentially followed by fractionated radiotherapy or radiosurgery. Except for bevacizumab in neurofibromatosis type 2, there is no role for pharmacotherapy.
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              Hearing preservation in unilateral acoustic neuroma surgery.

              This paper reviews the principal English literature on hearing preservation in unilateral acoustic neuroma surgery. Seventeen case reports and 13 surgical series are included. In addition, we report ten cases of our own, two with successful hearing preservation. The purpose of this report is to study feasibility, success rate, and associated problems. Previous reports have been compared in terms of criteria that we have selected. A classification system similar to Silverstein's is used. The total number of cases under review is 621, with 221 reported successes. Cases limited to those having a unilateral acoustic neuroma, with valid supportive audiometry, were 394, with 131 successes. The approximate overall rate of success is 33%. There are five cases of hearing preservation with unilateral acoustic neuromas 3 cm or larger when supporting audiometric data are available, the largest being "4-5 centimeters." Problems included mixing of unilateral acoustic neuromas with other types of tumors and failure to include comprehensive data, particularly audiometry. We conclude 1) that hearing preservation is a reasonable goal in unilateral acoustic neuroma surgery, although the number of available candidates is relatively small and 2) that intelligent selection of patients and high quality surgical technique are the keys to success.
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                Author and article information

                Contributors
                Journal
                Neurooncol Adv
                Neurooncol Adv
                noa
                Neuro-Oncology Advances
                Oxford University Press (US )
                2632-2498
                Jan-Dec 2024
                03 November 2023
                03 November 2023
                : 6
                : 1
                : vdad144
                Affiliations
                Department of Otolaryngology, Radboud University Medical Center , Nijmegen, The Netherlands
                Department of Otolaryngology, Maastricht University Medical Center+ , Maastricht, The Netherlands
                Dutch Academic Alliance Skull Base Pathology Radboudumc/MUMC+ , Nijmegen and Maastricht, The Netherlands
                Gamma Knife Center, Department of Neurosurgery, Elisabeth-TweeSteden Hospital , Tilburg, The Netherlands
                Gamma Knife Center, Department of Neurosurgery, Elisabeth-TweeSteden Hospital , Tilburg, The Netherlands
                Eindhoven University of Technology , Eindhoven, The Netherlands
                Gamma Knife Center, Department of Neurosurgery, Elisabeth-TweeSteden Hospital , Tilburg, The Netherlands
                Eindhoven University of Technology , Eindhoven, The Netherlands
                Department of Otolaryngology, Radboud University Medical Center , Nijmegen, The Netherlands
                Dutch Academic Alliance Skull Base Pathology Radboudumc/MUMC+ , Nijmegen and Maastricht, The Netherlands
                Department of Otolaryngology, Radboud University Medical Center , Nijmegen, The Netherlands
                Dutch Academic Alliance Skull Base Pathology Radboudumc/MUMC+ , Nijmegen and Maastricht, The Netherlands
                Department of Otolaryngology, Radboud University Medical Center , Nijmegen, The Netherlands
                Dutch Academic Alliance Skull Base Pathology Radboudumc/MUMC+ , Nijmegen and Maastricht, The Netherlands
                Gamma Knife Center, Department of Neurosurgery, Elisabeth-TweeSteden Hospital , Tilburg, The Netherlands
                Department of Otolaryngology, Radboud University Medical Center , Nijmegen, The Netherlands
                Department of Otolaryngology, Maastricht University Medical Center+ , Maastricht, The Netherlands
                Dutch Academic Alliance Skull Base Pathology Radboudumc/MUMC+ , Nijmegen and Maastricht, The Netherlands
                Author notes
                Corresponding Author: Sammy M. Schouten, MD, Department of Otolaryngology, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525 GA Nijmegen, The Netherlands ( sammy.schouten@ 123456radboudumc.nl ).
                Author information
                https://orcid.org/0009-0008-8098-1692
                Article
                vdad144
                10.1093/noajnl/vdad144
                10771273
                38187870
                5cf2d560-ebed-4024-b1f6-a98f96deb1c4
                © The Author(s) 2023. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 06 January 2024
                Page count
                Pages: 10
                Funding
                Funded by: Highly Specialised Care & Research;
                Funded by: Netherlands Organisation for Health Research and Development, DOI 10.13039/501100001826;
                Award ID: 10070012010006
                Categories
                Basic and Translational Investigations
                AcademicSubjects/MED00300
                AcademicSubjects/MED00310

                koos grade 4,observation,vestibular schwannoma,volumetric growth,wait-and-scan

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