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. 2017 Jul;133(3):609-614.
doi: 10.1007/s11060-017-2475-z. Epub 2017 Jun 7.

Clinical presentation and prognostic indicators in 100 adults and children with neurofibromatosis 1 associated non-optic pathway brain gliomas

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Clinical presentation and prognostic indicators in 100 adults and children with neurofibromatosis 1 associated non-optic pathway brain gliomas

Susan Byrne et al. J Neurooncol. 2017 Jul.

Abstract

Type 1 Neurofibromatosis (NF1) is a common autosomal dominant condition, with a major impact on the nervous system, eye, bone, and skin, and a predisposition to malignancy. At present it is not possible to predict clinically or on imaging, whether a brain tumour will remain indolent or undergo high-grade change. There are no consensus guidelines on the follow-up of non-optic pathway glioma (non-OPG) tumours in NF1. One hundred patients from the National NF1 Service with generalised NF1 and a diagnosis of non-OPG glioma were followed up for a median time of 63 months after glioma detection. Forty-two patients underwent surgical intervention. Ninety-one percent (38) of those requiring surgery did so within 5 years of diagnosis of glioma. Serial neuroimaging was undertaken in 88 patients. In 66 (75%), the lesion on the scan was stable or had improved at follow-up. High-grade lesions were present in five patients and were strongly associated with tumours in the thalamus (p = 0.001). Five patients died during follow-up. The diagnosis of high-grade glioma had a HR of 99.7 (95% CI 11.1-898.9, p < 000.1) on multivariate Cox regression to evaluate predictive factors related to death. In our cohort of 100 patients with NF1, we have shown that tumours in the thalamus are more likely to be associated with radiological progression, high-grade tumours, and surgical intervention. As a result of this finding, heightened surveillance with more frequent imaging should be considered in thalamic involvement. We have also demonstrated that over 40% of patients underwent surgery, and did so within 5 years of tumour diagnosis. Serial imaging should be undertaken for at the very least, 5 years from tumour detection.

Keywords: Brain tumour; Epidemiology; Neurofibromatosis type 1 (NF1); Neurooncology; Pilocytic astrocytoma; Thalamic tumour.

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Conflict of interest statement

Conflict of interest

None of the authors have any conflicts of interest to declare in relation to this project.

Ethical approval

This study was approved as a clinical evaluation with study number 5099 by the Clinical Audit Group Committee at Guy’s and St. Thomas’ NHS Foundation Trust, London.

Figures

Fig. 1
Fig. 1
Venn diagram of location of non-OPG (n = 100)
Fig. 2
Fig. 2
Flow diagram of the requirement for surgery in 100 patients with NF1 related glioma (immediate surgery refers to surgery within 2 months of initial presentation, HGG high grade glioma)

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