Your browser doesn't support javascript.
loading
Stereotactic radiosurgery for non-vestibular cranial nerve schwanommas.
D'Astous, Myreille; Ho, Allen L; Pendharkar, Arjun; Choi, Clara Y H; Soltys, Scott G; Gibbs, Iris C; Tayag, Armine T; Thompson, Patricia A; Adler, John R; Chang, Steven D.
Afiliação
  • D'Astous M; Department of Neurosurgery, Stanford University Medical Center, Stanford Cancer Institute, Stanford, CA, USA. myreille.dastous.1@ulaval.ca.
  • Ho AL; Department of Surgery, CHU de Québec, Université Laval, Quebec City, QC, Canada. myreille.dastous.1@ulaval.ca.
  • Pendharkar A; Department of Neurosurgery, Stanford University Medical Center, Stanford Cancer Institute, Stanford, CA, USA.
  • Choi CY; Department of Neurosurgery, Stanford University Medical Center, Stanford Cancer Institute, Stanford, CA, USA.
  • Soltys SG; Department of Radiation Oncology, Stanford University Medical Center, Stanford Cancer Institute, Stanford, CA, USA.
  • Gibbs IC; Department of Radiation Oncology, Stanford University Medical Center, Stanford Cancer Institute, Stanford, CA, USA.
  • Tayag AT; Department of Radiation Oncology, Stanford University Medical Center, Stanford Cancer Institute, Stanford, CA, USA.
  • Thompson PA; Department of Neurosurgery, Stanford University Medical Center, Stanford Cancer Institute, Stanford, CA, USA.
  • Adler JR; Department of Neurosurgery, Stanford University Medical Center, Stanford Cancer Institute, Stanford, CA, USA.
  • Chang SD; Department of Neurosurgery, Stanford University Medical Center, Stanford Cancer Institute, Stanford, CA, USA.
J Neurooncol ; 131(1): 177-183, 2017 01.
Article em En | MEDLINE | ID: mdl-27752881
ABSTRACT
Non-vestibular cranial nerve schwannomas (NVCNS) are rare lesions, representing <10 % of cranial nerve schwannomas. The optimal treatment for NVCNS is often derived from vestibular schwannomas experience. Surgical resection has been referred to as the first line treatment for those benign tumors, but significant complication rates are reported. Stereotactic radiosurgery (SRS) has arisen as a mainstay of treatment for many benign tumors, including schwanommas. We retrospectively reviewed the outcomes of NVCNS treated by SRS to characterize tumor control, symptom relief, toxicity, and the role of hypo-fractionation of SRS dose. Eighty-eight (88) patients, with ninety-five (95) NVCNS were treated with either single or multi-session SRS from 2001 to 2014. Local control was achieved in 94 % of patients treated (median follow-up of 33 months, range 1-155). Complications were seen in 7.4 % of cases treated with SRS. At 1-year, 57 % of patients had improvement or resolution of their symptoms, while 35 % were stable and 8 % had worsening or increased symptoms. While 42 % received only one session, results on local control were similar for one or multiple sessions (p = 0.424). SRS for NVCNS is a treatment modality that provides excellent local control with minimal complication risk compared to traditional neurosurgical techniques. Tumor control obtained with a multi-session treatment was not significantly different from single session treatment. Safety profile was also comparable for uni or multi-session treatments. We concluded that, as seen in VS treated with CK SRS, radiosurgery treatment can be safely delivered in cases of NVCNS.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Resultado do Tratamento / Radiocirurgia / Neoplasias dos Nervos Cranianos / Neurilemoma Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurooncol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Resultado do Tratamento / Radiocirurgia / Neoplasias dos Nervos Cranianos / Neurilemoma Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurooncol Ano de publicação: 2017 Tipo de documento: Article