Your browser doesn't support javascript.
loading
WHO grade II meningioma: a retrospective study for outcome and prognostic factor assessment.
Champeaux, Charles; Wilson, Elena; Shieff, Colin; Khan, Akbar Ali; Thorne, Lewis.
Afiliação
  • Champeaux C; Victor Horsley Department of Neurosurgical, National Hospital for Neurology and Neurosurgery, 33 Queen Square, London, WC1N 3BG, UK. Charles.Champeaux@gmail.com.
  • Wilson E; Department of Clinical Oncology, University College London Hospitals NHS Foundation Trust, London, NW1 2BU, UK.
  • Shieff C; Victor Horsley Department of Neurosurgical, National Hospital for Neurology and Neurosurgery, 33 Queen Square, London, WC1N 3BG, UK.
  • Khan AA; Victor Horsley Department of Neurosurgical, National Hospital for Neurology and Neurosurgery, 33 Queen Square, London, WC1N 3BG, UK.
  • Thorne L; Victor Horsley Department of Neurosurgical, National Hospital for Neurology and Neurosurgery, 33 Queen Square, London, WC1N 3BG, UK.
J Neurooncol ; 129(2): 337-45, 2016 09.
Article em En | MEDLINE | ID: mdl-27311726
ABSTRACT
To analyse the outcome of patients with WHO grade II meningioma and identify factors that may influence recurrence and survival. Between January 2007 and September 2015, a retrospective search identified 194 WHO grade II meningiomas at the National Hospital for Neurology and Neurosurgery, London. Survival methods were implemented. 31 patients (16 %) had a previous history of grade I meningioma. The patients underwent a total of 344 surgical resections and 43.3 % received radiotherapy. 55 patients (28.4 %) had been re-operated on for a WHO grade II meningioma relapse. Median follow-up was 4.4 years. At the end of the study, 75 patients (40.1 %) had no residual tumour on the last scan. Surgical recurrence free survival at 5 years was 71.6, 95 % CI [63.5, 80.8]. Secondary grade II meningioma (HR = 2.29, p = 0.010), and, Simpson resection grade 1, 2 and 3 vs. 4 and 5 (HR = 0.57, p = 0.050) were associated with the surgical recurrence-free survival. 32 died from meningioma (16.5 %). Overall survival probability at 5 years was 83.2, 95 % CI [76.6, 90.4]. Age at diagnosis (HR = 0.22, p < 0.001), WHO grade I meningioma progressing into grade II (HR = 3.2, p = 0.001), tumour location (HR = 0.19, p < 0.001), and mitosis count (HR = 0.36, p = 0.010) were independently associated with the overall survival. Patients who received radiotherapy demonstrated neither a reduced risk of recurrence nor a longer overall survival (p = 0.310). In our series shorter survival correlated with older age, increased mitoses, progression from grade I to II and location. We were not able to demonstrate a significant improvement in any of the clinical outcomes after radiotherapy.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Resultado do Tratamento / Procedimentos Neurocirúrgicos / Neoplasias Meníngeas / Meningioma Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurooncol Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 Base de dados: MEDLINE Assunto principal: Resultado do Tratamento / Procedimentos Neurocirúrgicos / Neoplasias Meníngeas / Meningioma Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurooncol Ano de publicação: 2016 Tipo de documento: Article