Refining the Intraoperative Identification of Suspected High-Grade Glioma Using a Surgical Fluorescence Biomarker: GALA BIDD Study Report

Author:

Watts Colin1,Dayimu Alimu2ORCID,Matys Tomasz3ORCID,Ashkan Keyoumars4,Price Stephen5ORCID,Jenkinson Michael D.6ORCID,Doughton Gail7,Mather Claire7,Young Gemma7,Qian Wendi7,Kurian Kathreena M.8ORCID

Affiliation:

1. Academic Department of Neurosurgery Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham B15 2TT, UK

2. Clinical Trials Unit, Department of Oncology, University of Cambridge, Cambridge CB2 0QQ, UK

3. Department of Radiology, University of Cambridge, and Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge CB2 0QQ, UK

4. Department of Neurosurgery, King’s College Hospital, London SE5 9RS, UK

5. Academic Neurosurgery Unit, Department of Clinical Neurosciences, University of Cambridge, Cambridge CB2 0QQ, UK

6. Department of Neurosurgery, Walton Centre, University of Liverpool, Liverpool L9 7LJ, UK

7. Cambridge Clinical Trials Unit—Cancer Theme (CCTU-CT), Cambridge CB2 0QQ, UK

8. Brain Tumour Research Centre, University of Bristol Medical School & North Bristol Trust, Bristol BS10 5NB, UK

Abstract

Background. Improving intraoperative accuracy with a validated surgical biomarker is important because identifying high-grade areas within a glioma will aid neurosurgical decision-making and sampling. Methods. We designed a multicentre, prospective surgical cohort study (GALA-BIDD) to validate the presence of visible fluorescence as a pragmatic intraoperative surgical biomarker of suspected high-grade disease within a tumour mass in patients undergoing 5-aminolevulinic acid (5-ALA) fluorescence-guided cytoreductive surgery. Results. A total of 106 patients with a suspected high-grade glioma or malignant transformation of a low-grade glioma were enrolled. Among the 99 patients who received 5-ALA, 89 patients were eligible to assess the correlation of fluorescence with diagnosis as per protocol. Of these 89, 81 patients had visible fluorescence at surgery, and 8 patients had no fluorescence. A total of 80 out of 81 fluorescent patients were diagnosed as high-grade gliomas on postoperative central review with 1 low-grade glioma case. Among the eight patients given 5-ALA who did not show any visible fluorescence, none were high-grade gliomas, and all were low-grade gliomas. Of the seven patients suspected radiologically of malignant transformation of low-grade gliomas and with visible fluorescence at surgery, six were diagnosed with high-grade gliomas, and one had no tissue collected. Conclusion. In patients where there is clinical suspicion, visible 5-ALA fluorescence has clinical utility as an intraoperative surgical biomarker of high-grade gliomas and can aid surgical decision-making and sampling. Further studies assessing the use of 5-ALA to assess malignant transformation in all diffuse gliomas may be valuable.

Funder

Cancer Research UK

NIHR Cambridge Biomedical Research Centre

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

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