Purpose
The objective of this study is to assess visual outcome, tumour control and treatment-related toxicities in patients with primary ONSM in an Australian institution.
Methods and materials
Patients with a diagnosis of primary ONSM were extracted from a prospective institutional database between January 2004 and December 2013. Patients with meningiomas of the sphenoid wing or planum sphenoidale with secondary involvement of the optic nerve were excluded.
Patients were treated with radiotherapy with multiple non-coplanar dynamic conformal technique using a Novalis TX linear accelerator with ExacTrac image guidance. Treatment doses varied from a mildly hypofractionated approach of 37.5 Gy in 15 fractions to conventionally fractionated 50.4-54 Gy in 28-30 fractions, prescribed to the...
Results
Patient and Treatment Characteristics
26 patients with ONSM treated with SRT met the criteria for inclusion in the study. All patients had unilateral diseases and were diagnosed based on characteristic radiological appearance of ONSM on MRI. The median duration of clinical follow-up was 68 months post-SRT (range 20 to 134 months).
Visual Outcomes
In the 10 patients with proptosis on presentation, 4 had a reduction in proptosis measured on exophthalmometry, 2 remained stable and 6 had no post-treatment data to assess response. In the three...
Conclusion
Patients with primary ONSM treated with SRT had excellent and durable local tumour control on MRI follow-up.
Our series found that a greater proportion of patients with good vision pre-SRT had stable or improved vision indicating that early treatment should be considered in patients prior to visual deterioration.
References
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