Long-term treatment outcomes of patients with primary optic nerve sheath meningioma treated with stereotactic radiotherapy

2019 ◽  
Vol 68 ◽  
pp. 162-167 ◽  
Author(s):  
Gishan Ratnayake ◽  
Tracy Oh ◽  
Rhuju Mehta ◽  
Thomas Hardy ◽  
Katrina Woodford ◽  
...  
2018 ◽  
Vol 103 (10) ◽  
pp. 1436-1440 ◽  
Author(s):  
Ravi Pandit ◽  
Liliana Paris ◽  
Danielle S Rudich ◽  
Robert L Lesser ◽  
Mark J Kupersmith ◽  
...  

Background/AimFractionated conformal radiotherapy (FCRT) is now used to treat vision-threatening optic nerve sheath meningioma (ONSM), but long-term efficacy and safety data are lacking; the purpose of this study was to assess these key data.MethodsThis is a retrospective chart review with prospective follow-up of adult patients treated with FCRT for primary ONSM at four academic medical centres between 1995 and 2007 with ≥10 years of follow-up after treatment.Results16 patients were identified with a mean post-treatment follow-up of 14.6 years (range: 10.5–20.7 years). The mean age at symptom onset was 47.6 years (range: 36–60 years). FCRT was performed at a mean of 2.3 years after symptom onset (range: 0.2–14.0 years). At last follow-up, visual acuity had improved or stabilised in 14 of the 16 (88%) patients, and 11 (69%) had retained or achieved ≥20/40. The mean deviation on automated perimetry remained stable (−14.5 dB pretreatment vs −12.2 dB at last follow-up; p=0.68, n=10). Two (11%) patients had persistent pain, proptosis or diplopia, compared with six (38%) pretreatment (p=0.11). Two (13%) patients developed radiation retinopathy more than 6 months after completion of therapy, one (50%) of whom had worse visual acuity compared with pretreatment. No patient developed tumour involvement or radiation damage in the fellow eye.ConclusionFCRT stabilises or improves visual function in patients with primary ONSM and is associated with a low risk of significant ocular sequelae. This treatment should be considered instead of surgery in patients with primary ONSM who require intervention due to loss of visual sensory and/or ocular motor function.


2004 ◽  
Vol 72 (2) ◽  
pp. 169-174 ◽  
Author(s):  
Brigitta G Baumert ◽  
Salvador Villà ◽  
Gabriela Studer ◽  
René-Olivier Mirimanoff ◽  
J.Bernard Davis ◽  
...  

2017 ◽  
Vol 102 (8) ◽  
pp. 1147-1153 ◽  
Author(s):  
Daniel S Narayan ◽  
Ghislaine L Traber ◽  
Edwin Figueira ◽  
Adnan Pirbhai ◽  
Klara Landau ◽  
...  

PurposeTo study the natural history, clinical and radiological characteristics of primary paediatric optic nerve sheath meningioma (PPONSM).MethodsRetrospective study of eight paediatric patients who were treated between 1994 and 2016 at the University Hospital Zurich, Switzerland and the Royal Adelaide Hospital, Australia. Clinical records and imaging studies were reviewed.ResultsThe mean age at presentation was 11 years (range: 6–17 years). There were six female patients and two male patients. 2/8 patients had associated neurofibromatosis type 2. Patients were followed up for 71–297 months (mean 156±70 months). 6/8 patients were observed through the course of their disease and 2/8 patients were treated with radiotherapy. 2/8 patients who were observed had minimal change in vision and did not experience tumour growth after long-term follow-up.ConclusionsThis is the largest PPONSM case series with long-term data on patients treated conservatively. We highlight that a small subset of these tumours are indolent and can be managed using observation alone.


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