Abstract
We retrospectively reviewed records of 33 consecutive trigeminal schwannoma patients who underwent Gamma Knife® SRS. Two patients had neurofibromatosis type 2. The median patient age was 49 years (range, 15–82 years). Eleven patients had prior surgical resection of their tumors. The tumors were classified into root type (N = 6), ganglion type (N = 17) and dumbbell type (N = 10) based on their location. The median tumor volume was 4.2 cc (range, 0.5–18.0 cc) and the median marginal dose was 15.0 Gy (range, 12–20 Gy). At an average of 6 years (range, 7.2–147.9 months), the progression free survival after SRS at 1-, 5- and 10 years, respectively was 97%, 82% and 82%. Factors associated with an improved progression free survival included female gender, smaller tumor volume, and root or ganglion type tumors. Neurological symptoms or signs improved in 11 of 33 patients (33%) and unchanged in 19 patients (58%). Three patients (9%) had symptomatic progression. Patients without prior resection were significantly more likely to have improvement in neurological symptoms or signs. Predictors of better response included female gender, smaller volume, root and ganglion type tumors, and use of SRS as the primary management.
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Kano, H., Kondziolka, D., Niranjan, A., Flickinger, J.C., Lunsford, L.D. (2012). Stereotactic Radiosurgery for Trigeminal Schwannoma: Tumor Control and Functional Preservation. In: Hayat, M. (eds) Tumors of the Central Nervous System, Volume 7. Tumors of the Central Nervous System, vol 7. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-2894-3_30
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