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Dive into the research topics where Patrick Murray is active.

Publication


Featured researches published by Patrick Murray.


British Journal of Radiology | 2017

A systematic review of outcomes following Stereotactic Ablative Radiotherapy in the treatment of early stage primary lung cancer.

Patrick Murray; K. Franks; G.G. Hanna

Stereotactic ablative body radiotherapy (SABR) describes a radiotherapy (RT) technique where high doses of radiation are precisely delivered to an extracranial target within the body, using either a single fraction of RT or using multiple small numbers of fractions. SABR has now become the standard of care treatment for patients with early-stage non-small-cell lung cancer (NSCLC) for whom surgery is not appropriate. This systematic review considers the evidence supporting the use of SABR in early-stage NSCLC, reported toxicity rates, the use of SABR in centrally located NSCLC, the use of SABR as salvage therapy following surgery or RT, and future potential drug combinations with SABR.


Clinical Oncology | 2016

Superiority of deformable image co-registration in the integration of diagnostic positron emission tomography-computed tomography to the radiotherapy treatment planning pathway for oesophageal carcinoma

G. Ward; S. Ramasamy; J.R. Sykes; Robin Prestwich; F. Chowdhury; A. Scarsbrook; Patrick Murray; K. Harris; A. Crellin; P. Hatfield; D. Sebag-Montefiore; Emiliano Spezi; Tom Crosby; G. Radhakrishna

AIMS To investigate the use of image co-registration in incorporating diagnostic positron emission tomography-computed tomography (PET-CT) directly into the radiotherapy treatment planning pathway, and to describe the pattern of local recurrence relative to the PET-avid volume. MATERIALS AND METHODS Fourteen patients were retrospectively identified, six of whom had local recurrence. The accuracy of deformable image registration (DIR) and rigid registration of the diagnostic PET-CT and recurrence CT, to the planning CT, were quantitatively assessed by comparing co-registration of oesophagus, trachea and aorta contours. DIR was used to examine the correlation between PET-avid volumes, dosimetry and site of recurrence. RESULTS Positional metrics including the dice similarity coefficient (DSC) and conformity index (CI), showed DIR to be superior to rigid registration in the co-registration of diagnostic and recurrence imaging to the planning CT. For diagnostic PET-CT, DIR was superior to rigid registration in the transfer of oesophagus (DSC=0.75 versus 0.65, P<0.009 and CI=0.59 versus 0.48, P<0.003), trachea (DSC=0.88 versus 0.65, P<0.004 and CI=0.78 versus 0.51, P<0.0001) and aorta structures (DSC=0.93 versus 0.86, P<0.006 and CI=0.86 versus 0.76, P<0.006). For recurrence imaging, DIR was superior to rigid registration in the transfer of trachea (DSC=0.91 versus 0.66, P<0.03 and CI=0.83 versus 0.51, P<0.02) and oesophagus structures (DSC=0.74 versus 0.51, P<0.004 and CI=0.61 versus 0.37, P<0.006) with a non-significant trend for the aorta (DSC=0.91 versus 0.75, P<0.08 and CI=0.83 versus 0.63, P<0.06) structure. A mean inclusivity index of 0.93 (range 0.79-1) showed that the relapse volume was within the planning target volume (PTVPET-CT); all relapses occurred within the high dose region. CONCLUSION DIR is superior to rigid registration in the co-registration of PET-CT and recurrence CT to the planning CT, and can be considered in the direct integration of PET-CT to the treatment planning process. Local recurrences occur within the PTVPET-CT, suggesting that this is a suitable target for dose-escalation strategies.


Clinical Oncology | 2018

Effectiveness of Respiratory-gated Positron Emission Tomography/Computed Tomography for Radiotherapy Planning in Patients with Lung Carcinoma – A Systematic Review

R. Frood; Robin Prestwich; C. Tsoumpas; Patrick Murray; K. Franks; Andrew Scarsbrook

AIMS A systematic review of the literature evaluating the clinical use of respiratory-gated (four-dimensional; 4D) fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT) compared with non-gated (three-dimensional; 3D) PET/CT for radiotherapy planning in lung cancer. MATERIALS AND METHODS A search of MEDLINE, Cochrane, Web of Science, SCOPUS and clinicaltrials.gov databases was undertaken for articles comparing 3D and 4D PET/CT tumour volume or 4D PET/CT for radiotherapy planning. PRISMA guidelines were followed. RESULTS Thirteen studies compared tumour volumes at 3D and 4D PET/CT; eight reported significantly smaller volumes (6.9-44.5%), three reported significantly larger volumes at 4D PET/CT (16-50%), one reported no significant difference and one reported mixed findings. Six studies, including two that reported differences in tumour volumes, compared target volumes or studied geographic misses. 4D PET/CT target volumes were significantly larger (19-40%) when compared with 3D PET/CT in all but one study, where they were smaller (3.8%). One study reported no significance in 4D PET/CT target volumes when compared with 4D CT, whereas another study reported significantly larger volumes (38.7%). CONCLUSION The use of 4D PET/CT leads to differences in target volume delineation compared with 3D PET/CT. These differences vary depending upon technique and the clinical impact currently remains uncertain. Correlation of pretreatment target volumes generated at 3D and 4D PET/CT with postsurgical histology would be ideal but technically challenging. Evaluation of patient outcomes based on 3D versus 4D PET/CT derived treatment volumes warrants further investigation.


Clinical Oncology | 2016

Benefits of Stereotactic Radiotherapy Fellowships to Clinical Oncology Trainees

I. Phillips; K. Thippu Jayaprakash; Patrick Murray

Madam e As Clinical Research Fellows in stereotactic radiotherapy, we recognise the growing benefit of acquiring greater technical skills in advanced radiotherapy during our clinical oncology training. Our involvement in the development of new stereotactic radiotherapy services has helped us to understand the background process in delivering a new treatment technique. This includes the commissioning process, designing treatment protocols and departmental pathways for implementing a new radiotherapy technique and the importance of multidisciplinary working. In the radiotherapy planning pathway we have hadmore exposure to imaging in both the selection of suitable patients and tumour localisation. We have also had more time to devote to radiotherapy planning [1]. Benefits include gaining familiarity with new positron emission tomography tracers, potential extension of magnetic resonance imaging and the role of rigid and deformable registration in radiotherapy planning. We now have a greater understanding of volumetric and fiducial-based image guidance, motion management strategies and online/real-time verification. These specific skills are generally notwell developed in our training [2].Weneed to be able to act on changes seen at planning and treatment delivery to know when it is appropriate to treat and when there may be a need for an urgent re-plan. Our fellowships have helped to develop our clinical judgement, giving us more confidence to act independently as consultants. Frequent discussions and presentations on stereotactic radiotherapy to specialist and non-specialist audiences,


Radiotherapy and Oncology | 2018

Long term patient reported swallowing function following chemoradiotherapy for oropharyngeal carcinoma

Lynne Dixon; S. Ramasamy; Kate Cardale; Karen E. Dyker; Kate Garcez; Lip W Lee; Andrew McPartlin; Patrick Murray; Mehmet Sen; N. Slevin; Andrew J Sykes; Robin Prestwich; David J Thomson


Radiotherapy and Oncology | 2018

EP-1452: Safety & tolerability of radiotherapy dose escalation in cervical-upper thoracic oesophageal cancer

C. Jones; Patrick Murray; R. Goody; G. Ward; N. Casanova; Paul Hatfield; G. Radhakrishna


Journal of Thoracic Oncology | 2018

P2.16-17 Hypo-Fractionated Accelerated Radiotherapy in Central Early Non-Small Cell Lung Cancer: Leeds Cancer Centre Experience

T. Janjua; M. Arunsingh; K. Clarke; P. Dickinson; K. Franks; Patrick Murray; Michael Snee; M. Teo; P. Jain


Journal of Thoracic Oncology | 2017

P1.05-030 Lung SABR for Early Stage Lung Cancer: Outcomes and Toxicity of 803 Patients Treated at the Leeds Cancer Centre: Topic: SBRT

Patrick Murray; K. Clarke; K. Franks; P. Dickinson; J. Lilley; Michael Snee; Pooja Jain


Clinical Oncology | 2017

Small cell cancer of the oesophagus – a network series

Amy Martin; L. Murray; Patrick Murray; Rebecca Goody; Paul Hatfield; Adrian Crellin; Nigel Scott; Christopher Fosker; S. Ramasamy; G. Radhakrishna


BMC Cancer | 2017

Respiratory-gated (4D) contrast-enhanced FDG PET-CT for radiotherapy planning of lower oesophageal carcinoma: feasibility and impact on planning target volume

Andrew Scarsbrook; Gillian Ward; Patrick Murray; Rebecca Goody; Karen Marshall; Garry McDermott; Robin Prestwich; G. Radhakrishna

Collaboration


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K. Franks

St James's University Hospital

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G. Radhakrishna

St James's University Hospital

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Robin Prestwich

St James's University Hospital

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S. Ramasamy

Leeds Teaching Hospitals NHS Trust

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K. Clarke

University of Toronto

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G.G. Hanna

Queen's University Belfast

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Michael Snee

St James's University Hospital

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Paul Hatfield

St James's University Hospital

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Rebecca Goody

Leeds Teaching Hospitals NHS Trust

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