J. Conway
Weston Park Hospital
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Featured researches published by J. Conway.
Radiotherapy and Oncology | 2001
Christopher M. Nutting; Carl G Rowbottom; Vivian P Cosgrove; J.Michael Henk; David P. Dearnaley; Martin Robinson; J. Conway; Steve Webb
BACKGROUND AND PURPOSE To compare external beam radiotherapy techniques for parotid gland tumours using conventional radiotherapy (RT), three-dimensional conformal radiotherapy (3DCRT), and intensity-modulated radiotherapy (IMRT). To optimise the IMRT techniques, and to produce an IMRT class solution. MATERIALS AND METHODS The planning target volume (PTV), contra-lateral parotid gland, oral cavity, brain-stem, brain and cochlea were outlined on CT planning scans of six patients with parotid gland tumours. Optimised conventional RT and 3DCRT plans were created and compared with inverse-planned IMRT dose distributions using dose-volume histograms. The aim was to reduce the radiation dose to organs at risk and improve the PTV dose distribution. A beam-direction optimisation algorithm was used to improve the dose distribution of the IMRT plans, and a class solution for parotid gland IMRT was investigated. RESULTS 3DCRT plans produced an equivalent PTV irradiation and reduced the dose to the cochlea, oral cavity, brain, and other normal tissues compared with conventional RT. IMRT further reduced the radiation dose to the cochlea and oral cavity compared with 3DCRT. For nine- and seven-field IMRT techniques, there was an increase in low-dose radiation to non-target tissue and the contra-lateral parotid gland. IMRT plans produced using three to five optimised intensity-modulated beam directions maintained the advantages of the more complex IMRT plans, and reduced the contra-lateral parotid gland dose to acceptable levels. Three- and four-field non-coplanar beam arrangements increased the volume of brain irradiated, and increased PTV dose inhomogeneity. A four-field class solution consisting of paired ipsilateral coplanar anterior and posterior oblique beams (15, 45, 145 and 170 degrees from the anterior plane) was developed which maintained the benefits without the complexity of individual patient optimisation. CONCLUSIONS For patients with parotid gland tumours, reduction in the radiation dose to critical normal tissues was demonstrated with 3DCRT compared with conventional RT. IMRT produced a further reduction in the dose to the cochlea and oral cavity. With nine and seven fields, the dose to the contra-lateral parotid gland was increased, but this was avoided by optimisation of the beam directions. The benefits of IMRT were maintained with three or four fields when the beam angles were optimised, but were also achieved using a four-field class solution. Clinical trials are required to confirm the clinical benefits of these improved dose distributions.
Radiotherapy and Oncology | 2008
Christopher Mark Bragg; Katrina Wingate; J. Conway
PURPOSE To determine the implications of the use of the Anisotropic Analytical Algorithm (AAA) for the production and dosimetric verification of IMRT plans for treatments of the prostate, parotid, nasopharynx and lung. METHODS 72 IMRT treatment plans produced using the Pencil Beam Convolution (PBC) algorithm were recalculated using the AAA and the dose distributions compared. Twenty-four of the plans were delivered to inhomogeneous phantoms and verification measurements made using a pinpoint ionisation chamber. The agreement between the AAA and measurement was determined. RESULTS Small differences were seen in the prostate plans, with the AAA predicting slightly lower minimum PTV doses. In the parotid plans, there were small increases in the lens and contralateral parotid doses while the nasopharyngeal plans revealed a reduction in the volume of the PTV covered by the 95% isodose (the V(95%)) when the AAA was used. Large changes were seen in the lung plans, the AAA predicting reductions in the minimum PTV dose and large reductions in the V(95%). The AAA also predicted small increases in the mean dose to the normal lung and the V(20). In the verification measurements, all AAA calculations were within 3% or 3.5mm distance to agreement of the measured doses. CONCLUSIONS The AAA should be used in preference to the PBC algorithm for treatments involving low density tissue but this may necessitate re-evaluation of plan acceptability criteria. Improvements to the Multi-Resolution Dose Calculation algorithm used in the inverse planning are required to reduce the convergence error in the presence of lung tissue. There was excellent agreement between the AAA and verification measurements for all sites.
International Journal of Radiation Oncology Biology Physics | 2002
Christopher Mark Bragg; J. Conway; Martin Robinson
PURPOSE To compare intensity-modulated radiotherapy (IMRT) treatment plans with three-dimensional conformal radiotherapy (3D-CRT) plans to investigate the suitability of IMRT for the treatment of tumors of the parotid gland. METHODS AND MATERIALS One 3D-CRT treatment plan and 10 IMRT treatment plans with differing beam arrangements were produced for each of nine patient data sets. The plans were compared using regret analysis, dose conformity, dose to organs at risk, and uncomplicated tumor control probability (UTCP). RESULTS The target dose was comparable in the 3D-CRT and IMRT plans, although improvements were seen when seven and nine IMRT fields were used. IMRT reduced the mean dose to the contralateral parotid gland and the maximum doses to the brain and the spinal cord, but increased the ipsilateral lens dose in some cases. Each IMRT arrangement produced a higher UTCP than the 3D-CRT plans; the largest absolute difference was 9.6%. CONCLUSIONS IMRT is a suitable means for treating cancer of the parotid, and a five-field class solution is proposed. It produced substantial sparing of organs at risk and higher UTCPs than 3D-CRT and should enable dose escalation.
Radiotherapy and Oncology | 2001
Mark McJury; Patricia Fisher; Simon Pledge; Gillian Brown; Catherine Anthony; M.Q. Hatton; J. Conway; Martin Robinson
BACKGROUND AND PURPOSE Radiotherapy is widely used to palliate local symptoms in non-small-cell lung cancer. Using conventional X-ray simulation, it is often difficult to accurately localize the extent of the tumour. We report a randomized, double blind trial comparing target localization with conventional and virtual simulation. METHODS Eighty-six patients underwent both conventional and virtual simulation. The conventional simulator films were compared with digitally reconstructed radiographs (DRRs) produced from the computed tomography (CT) data. The treatment fields defined by the clinicians using each modality were compared in terms of field area, position and the implications for target coverage. RESULTS Comparing fields defined by each study arm, there was a major mis-match in coverage between fields in 66.2% of cases, and a complete match in only 5.2% of cases. In 82.4% of cases, conventional simulator fields were larger (mean 24.5+/-5.1% (95% confidence interval)) than CT-localized fields, potentially contributing to a mean target under-coverage of 16.4+/-3.5% and normal tissue over-coverage of 25.4+/-4.2%. CONCLUSIONS CT localization and virtual simulation allow more accurate definition of the target volume. This could enable a reduction in geographical misses, while also reducing treatment-related toxicity.
International Journal of Radiation Oncology Biology Physics | 2000
Jaap Vaarkamp; D C Barber; J. Conway; Martin Robinson
PURPOSE Accurate image registration is an essential step to integrate information from diagnostic and radiotherapy treatment planning (RTP) CT images. In this paper a fully automatic algorithm is presented to quickly register such diagnostic and RTP CT head scans. METHODS AND MATERIALS The registration algorithm, which regards one image as the moved version of the other, was applied to seven clinically obtained diagnostic and RTP CT data set pairs. During the RTP scan patients were in treatment position and wearing mold masks. Hence, patient position differed strongly in both image sets. Registrations were inspected visually and compared with results obtained minimizing the sum-of-square difference. RESULTS Registrations were accurate upon visual inspection. Differences between the two algorithms were at subvoxel level. All cases were successfully registered, using several different starting points. Registration calculations took 1-2 minutes. Minimization of the sum-of-square difference took 1-1.5 hours. CONCLUSIONS The results show that a fast and accurate image registration is achieved without prior segmentation or feature extraction and that the algorithm is robust, which makes it clinically applicable.
Journal of Radiotherapy in Practice | 2007
M. McJury; B. Foran; J. Conway; Simon Dixon; K. Wilcock; G. Brown; Martin Robinson
Background and purpose : Currently, optimal use of virtual simulation for all treatment sites is not entirely clear. This study presents data to identify specific patient groups for whom conventional simulation may be completely eliminated and replaced by virtual simulation. Sampling and method : Two hundred and sixty patients were recruited from four treatment sites (head and neck, breast, pelvis, and thorax). Patients were randomly assigned to be treated using the usual treatment process involving conventional simulation, or a treatment process differing only in the replacement of conventional plan verification with virtual verification. Data were collected on set-up accuracy at verification, and the number of unsatisfactory verifications requiring a return to the conventional simulator. A micro-economic costing analysis was also undertaken, whereby data for each treatment process episode were also collected: number and grade of staff present, and the time for each treatment episode. Results : The study shows no statistically significant difference in the number of returns to the conventional simulator for each site and study arm. Image registration data show similar quality of verification for each study arm. The micro-costing data show no statistical difference between the virtual and conventional simulation processes. Conclusions : At our institution, virtual simulation including virtual verification for the sites investigated presents no disadvantage compared to conventional simulation.
Journal of Radiotherapy in Practice | 2000
M. McJury; R. Nakielny; D. Levy; J. Lilley; J. Conway; Martin Robinson
Aims: To investigate the impact on localisation of utilising contrast enhanced computed tomography (CT) scans and the formal input of a radiologist in the radiotherapy planning process. Method: Ten head and neck / brain patients had pre- and post-contrast CT scans in the treatment position. Over several months, their unenhanced and enhanced scans were re-contoured by the original oncologist, and a radiologist. These new contours were compared to the original unenhanced contours and differences in contour volume, geographical position and tolerance doses on the associated PTVs were evaluated. Results: The use of contrast lead to significant differences in the size of GTVs. Mean differences in GTVs of 32.8 % were significant at p=0.01. No significant impact on the position of the contour centre was noted. The impact of the radiologist lead to large differences in GTV (mean 20.5 %), but large SDs meant this result was not statistically significant. The contouring precision of the oncologist showed no significant difference for GTVs and PTVs. Conclusions: The use of contrast when planning the radiotherapy treatment for head and neck / brain patients was found to lead to significant differences in GTV size, a lesser effect on PTV definition and little impact on the position of the contour centre. It may have important implications for multi-phase treatments where the GTV (rather than the PTV) is targeted for boost doses. Differences due to the input of a radiologist appear to be considerable and require further investigation when additional patient numbers have been acquired to improve precision.
Radiotherapy and Oncology | 2006
Christopher Mark Bragg; J. Conway
International Journal of Radiation Oncology Biology Physics | 2007
Rob H. Ireland; Karen E. Dyker; D C Barber; Steven Wood; Michael B. Hanney; Wendy Tindale; Neil Woodhouse; Nigel Hoggard; J. Conway; M.H. Robinson
Clinical Oncology | 2005
S.J. Clenton; Patricia Fisher; J. Conway; P. Kirkbride; M.Q. Hatton