Tara Barwick
Imperial College London
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Featured researches published by Tara Barwick.
Clinical Cancer Research | 2011
Kaiyumars B. Contractor; Amarnath Challapalli; Tara Barwick; Mathias Winkler; Giles Hellawell; Steve Hazell; Giampaolo Tomasi; Adil Al-Nahhas; Paola Mapelli; Laura M. Kenny; Paul Tadrous; R. Charles Coombes; Eric O. Aboagye; Stephen Mangar
Purpose: To evaluate the accuracy and biological basis for [11C]choline-PET-CT in the nodal staging of high risk localized prostate cancer patients. Experimental Design: Twenty-eight patients underwent dynamic [11C]choline-PET-CT of the pelvis and lower abdomen prior to extended laparoscopic pelvic lymph node dissection (eLPL). The sensitivity and specificity of [11C]choline PET, [11C]choline PET-CT, and MRI for nodal detection were calculated. Average and maximal standardized uptake values (SUVave, SUVmax) were compared with choline kinase alpha (CHKα) and Ki67 immunohistochemistry scores. Results: Four hundred and six lymph nodes (LN), in 26 patients, were assessable. Twenty-seven (6.7%) involved pelvic nodes at eLPL were detected in 9 patients. Seventeen of the 27 involved nodes were subcentimeter. The sensitivity and specificity on a per nodal basis were 18.5% and 98.7%, 40.7% and 98.4%, and 51.9% and 98.4% for MRI, [11C]choline PET, and [11C]choline PET-CT, respectively. Sensitivity was higher for [11C]choline PET-CT compared with MRI (P = 0.007). A higher nodal detection rate, including subcentimeter nodes, was seen with [11C]choline PET-CT than MRI. Malignant lesions showed CHKα expression in both cytoplasm and nucleus. SUVave and SUVmax strongly correlated with CHKα staining intensity (r = 0.68, P < 0.0001 and r = 0.63, P = 0.0004, respectively). In contrast, Ki67 expression was generally low in all tumors. Conclusion: This study establishes the relationship between [11C]choline PET-CT uptake with choline kinase expression in prostate cancer and allows it to be used as a noninvasive means of staging pelvic LNs, being highly specific and more sensitive than MRI, including the detection of subcentimeter disease. Clin Cancer Res; 17(24); 7673–83. ©2011 AACR.
Journal of Neurosurgery | 2017
Matthew Grech-Sollars; Babar Vaqas; Gerard Thompson; Tara Barwick; Lesley Honeyfield; Kevin O'Neill; Adam D. Waldman
OBJECTIVE Glioma heterogeneity and the limitations of conventional structural MRI for identifying aggressive tumor components can limit the reliability of stereotactic biopsy and, hence, tumor characterization, which is a hurdle for developing and selecting effective treatment strategies. In vivo MR spectroscopy (MRS) and PET enable noninvasive imaging of cellular metabolism relevant to proliferation and can detect regions of more highly active tumor. Here, the authors integrated presurgical PET and MRS with intraoperative neuronavigation to guide surgical biopsy and tumor sampling of brain gliomas with the aim of improving intraoperative tumor-tissue characterization and imaging biomarker validation. METHODS A novel intraoperative neuronavigation tool was developed as part of a study that aimed to sample high-choline tumor components identified by multivoxel MRS and 18F-methylcholine PET-CT. Spatially coregistered PET and MRS data were integrated into structural data sets and loaded onto an intraoperative neuronavigation system. High and low choline uptake/metabolite regions were represented as color-coded hollow spheres for targeted stereotactic biopsy and tumor sampling. RESULTS The neurosurgeons found the 3D spherical targets readily identifiable on the interactive neuronavigation system. In one case, areas of high mitotic activity were identified on the basis of high 18F-methylcholine uptake and elevated choline ratios found with MRS in an otherwise low-grade tumor, which revealed the possible use of this technique for tumor characterization. CONCLUSIONS These PET and MRI data can be combined and represented usefully for the surgeon in neuronavigation systems. This method enables neurosurgeons to sample tumor regions based on physiological and molecular imaging markers. The technique was applied for characterizing choline metabolism using MRS and 18F PET; however, this approach provides proof of principle for using different radionuclide tracers and other MRI methods, such as MR perfusion and diffusion.
Radiographics | 2016
Ioanna Papadopoulou; Victoria Stewart; Tara Barwick; Won-Ho Edward Park; Neil Soneji; Andrea G. Rockall; Nishat Bharwani
Locally advanced and node-positive cervical cancers are usually treated with external beam radiation therapy and intracavitary brachytherapy with concomitant chemotherapy. In patients with locally advanced cervical cancer, imaging plays a vital role in pretreatment planning, assessment of primary tumor response to treatment, follow-up, and evaluation of treatment-related complications. Radiation therapy planning is crucial to successful local and regional control of disease. Patient selection criteria for radiation therapy with concomitant chemotherapy are described, as is assessment of treatment response of the primary cervical tumor at magnetic resonance (MR) imaging. Image interpretation can be challenging because of radiation therapy-related changes in the pelvic organs. Expected changes in the bladder, bowel, and bone marrow after radiation therapy are described, and multimodality imaging findings at computed tomography, MR imaging, and fluorine 18 fluorodeoxyglucose positron emission tomography are illustrated. Complications after radiation therapy have declined over recent years because of targeted radiation therapy. These complications can be divided into acute and chronic effects, where acute toxic effects occur within weeks of treatment. Chronic complications include cervical stenosis, small bowel stricture, fistula formation, and insufficiency fractures. Imaging is an essential tool in the care of patients with cervical cancer treated with chemotherapy and radiation therapy. The reporting radiologist should be familiar with the expected imaging appearances of the pelvic organs after radiation therapy, as well as potential complications, to avoid pitfalls in image interpretation.
Journal of Neurology, Neurosurgery, and Psychiatry | 2017
Christopher James Carswell; Zarni Win; Kirsty Muckle; Angus Kennedy; Adam D. Waldman; Gemma Dawe; Tara Barwick; Sameer Khan; Paresh Malhotra; Richard J. Perry
Background and objective Amyloid-positron emission tomography (PET) imaging (API) detects amyloid-beta pathology early in the course of Alzheimer’s disease (AD) with high sensitivity and specificity. (18)F-florbetapir (Amyvid) is an amyloid-binding PET ligand with a half-life suitable for clinical use outside of the research setting. How API affects patient investigation and management in the ‘real-world’ arena is unknown. To address this, we retrospectively documented the effect of API in patients in the memory clinic. Methods We reviewed the presenting clinical features, the pre-API and post-API investigations, diagnosis and outcomes for the first 100 patients who had API as part of their routine work-up at the Imperial Memory Centre, a tertiary referral clinic in the UK National Health Service. Results API was primarily used to investigate patients with atypical clinical features (56 cases) or those that were young at onset (42 cases). MRI features of AD did not always predict positive API (67%), and 6 of 23 patients with MRIs reported as normal were amyloid-PET positive. There were significantly more cases categorised as non-AD dementia post-API (from 11 to 23). Patients investigated when API was initially available had fewer overall investigations and all patients had significantly fewer investigations in total post-API. Conclusions API has a clear impact on the investigation of young-onset or complex dementia while reducing the overall burden of investigations. It was most useful in younger patients, atypical presentations or individuals with multiple possible causes of cognitive impairment.
Radiographics | 2016
Anish Raithatha; Ioanna Papadopoulou; Victoria Stewart; Tara Barwick; Andrea G. Rockall; Nishat Bharwani
This presentation provides a pictorial correlation between the MR imaging appearances of cervical cancer and the FIGO (2009) staging system and highlights various pitfalls that may lead to misinterpretation. Furthermore, use of contrast-enhanced CT and FDG PET/CT for detection of distal spread of disease is demonstrated. The value of imaging in follow-up of recurrent disease is discussed.
Current Oncology Reports | 2017
Sairah R. Khan; Mubarik Arshad; Kathryn Wallitt; Victoria Stewart; Nishat Bharwani; Tara Barwick
Magnetic resonance imaging (MRI) is the optimal modality for local staging of gynecological tumors. Advances in functional MRI with diffusion-weighted and dynamic contrast-enhanced sequences provide more detailed information regarding tumor cellularity, vascularity, and viability. Fluorodeoxyglucose positron emission tomography/computed tomography (FDG PET/CT) now has an established role in imaging for gynecological cancers, particularly staging of locally advanced cervical cancers and pre-salvage exenterative therapy in relapsed gynecologic tumors. Novel PET tracers, targeting other aspects of tumor biology, are being evaluated although none are currently in routine clinical use. New PET/MR scanners have the potential to combine the strengths of both modalities in one sitting. This review covers advances in gynecologic imaging concentrating on cervical, endometrial, and ovarian cancers.
Archive | 2016
Sairah R. Khan; Tara Barwick
This chapter includes some case examples highlighting the use of PET/CT in gynaecological malignancies, demonstrating a number of important teaching points.
Archive | 2016
Sairah R. Khan; Tara Barwick
This chapter covers the use of PET/CT in gynaecological cancers concentrating on cervical, endometrial and ovarian cancers. The technical aspects and limitations of PET/CT specific to gynaecological malignancies are highlighted.
Jacc-cardiovascular Imaging | 2017
Taryn Youngstein; Enrico Tombetti; Jaita Mukherjee; Tara Barwick; Adil Al-Nahhas; Emyr Humphreys; Julian Nash; Jacqueline Andrews; Elena Incerti; Elisabetta Tombolini; Annalaura Salerno; Silvia Sartorelli; Giuseppe A. Ramirez; Maurizio Papa; Maria Grazia Sabbadini; Luigi Gianolli; Francesco De Cobelli; Federico Fallanca; Elena Baldissera; Angelo A. Manfredi; Maria Picchio; Justin C. Mason
European Journal of Nuclear Medicine and Molecular Imaging | 2015
Amarnath Challapalli; Tara Barwick; R. Pearson; Shairoz Merchant; Francesco Mauri; Elizabeth C. Howell; Katherine Anne Sumpter; Ross J. Maxwell; Eric O. Aboagye; Rohini Sharma