Matthew Grech-Sollars1,2, Babar Vaqas3, Gerard Thompson4, Tara Barwick2,5, Lesley Honeyfield2, Kevin S O'Neill3, and Adam D Waldman1,2
1Division of Brain Sciences, Imperial College London, London, United Kingdom, 2Department of Imaging, Imperial College NHS Healthcare Trust, London, United Kingdom, 3Department of Neurosurgery, Imperial College NHS Healthcare Trust, London, United Kingdom, 4Department of Neuroradiology, Salford Royal NHS Foundation Trust, Salford, United Kingdom, 5Department of Surgery and Cancer, Imperial College London, London, United Kingdom
Synopsis
Glioma heterogeneity and the
limitations of conventional structural MRI to identify agrressive tumour
components limits targeting of stereotactic biopsy, and hence tumour
characterisation. In vivo MR spectroscopy
and PET allow for physiological characterisation of tumour and we here present
a method for representing MRS and PET defined regions to biopsy using an ultrasound
based neuronavigational system. Our method involves using colour-coded hollow
spheres to represent the target biopsy regions, which can be easily identified
during the surgery. This approach can be applied to target the most aggressive
regions of a tumour and as a tool for imaging biomarker validation.Background:
Heterogeneity in
glioma limits tumour characterisation using stereotactic biopsy; it is
frequently not possible to accurately target the most aggressive tumour
components reliably from conventional structural imaging. In vivo MR spectroscopy (MRS) and PET allow
cellular metabolism relevant to proliferation to be imaged non-invasively.
Intra-operative ultrasound provides near real-time structural imaging for
surgical guidance. Here we combine PET and MRS with ultrasound neuro-navigation
to guide surgical biopsy for gliomas.
Methods:
An
intra-operative neuro-navigation tool was developed as part of a study to sample
high choline tumour components identified by MRS and 18F-methylcholine PET. 12
patients (7 male, 5 female; aged 23-73 years, mean 41 years) were recruited to
the study. Spatially co-registered PET and MRS data were integrated into
structural datasets and loaded onto a Neuronavigational 3D Ultrasound image
guidance system. High and low choline uptake/metabolite regions were
represented as colour coded hollow spheres for targeted biopsy (Figure 1).
Results:
The
operating surgeons found the 3D spherical targets readily identifiable on the
interactive navigation system and were able to register the images to the
pre-surgery images and overlay the ultrasound imaging to take into account
brain shift during surgery (Figures 2 and 3). In one case, areas of high
mitotic activity were identified on the basis of high 18F-methylcholine uptake
and elevated MRS choline ratios in an otherwise low-grade tumour.
Conclusions:
We
have developed a PET and MRS targeted stereotactic biopsy tool using
intraoperative ultrasound neuronavigation; this involves a combination of
proprietary and bespoke software to analyse and integrate physiological imaging
data, and novel presentation of biopsy targets as hollow spheres, which can readily
be identified in the operating environment. Our preliminary experiences indicate that
this method can be used to improve diagnostic accuracy of stereotactic biopsy. It also provides proof of principle for
spatially-correlated validation of a variety of imaging biomarkers against
tissue features.
Acknowledgements
This
work was part funded by the NIHR Imperial Comprehensive Biomedical Research
Centre. MGS is partly funded by The Brain Tumour Charity and Brain Tumour
Research Campaign. We would also like to thank Ms Sophie Camp, Dr Katherine Ordidge and Mr Daniel Darian for their help in this study. MRI and
PET imaging was carried out at the Imperial College Clinical Imaging Facility.References
No reference found.