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Featured researches published by J. Mason.


International Journal of Radiation Oncology Biology Physics | 2014

Prostate Stereotactic Ablative Radiation Therapy Using Volumetric Modulated Arc Therapy to Dominant Intraprostatic Lesions

L. Murray; J. Lilley; C.M. Thompson; V. Cosgrove; J. Mason; Jonathan R Sykes; K. Franks; David Sebag-Montefiore; Ann M. Henry

Purpose To investigate boosting dominant intraprostatic lesions (DILs) in the context of stereotactic ablative radiation therapy (SABR) and to examine the impact on tumor control probability (TCP) and normal tissue complication probability (NTCP). Methods and Materials Ten prostate datasets were selected. DILs were defined using T2-weighted, dynamic contrast-enhanced and diffusion-weighted magnetic resonance imaging. Four plans were produced for each dataset: (1) no boost to DILs; (2) boost to DILs, no seminal vesicles in prescription; (3) boost to DILs, proximal seminal vesicles (proxSV) prescribed intermediate dose; and (4) boost to DILs, proxSV prescribed higher dose. The prostate planning target volume (PTV) prescription was 42.7 Gy in 7 fractions. DILs were initially prescribed 115% of the PTVProstate prescription, and PTVDIL prescriptions were increased in 5% increments until organ-at-risk constraints were reached. TCP and NTCP calculations used the LQ-Poisson Marsden, and Lyman-Kutcher-Burman models respectively. Results When treating the prostate alone, the median PTVDIL prescription was 125% (range: 110%-140%) of the PTVProstate prescription. Median PTVDIL D50% was 55.1 Gy (range: 49.6-62.6 Gy). The same PTVDIL prescriptions and similar PTVDIL median doses were possible when including the proxSV within the prescription. TCP depended on prostate α/β ratio and was highest with an α/β ratio = 1.5 Gy, where the additional TCP benefit of DIL boosting was least. Rectal NTCP increased with DIL boosting and was considered unacceptably high in 5 cases, which, when replanned with an emphasis on reducing maximum dose to 0.5 cm3 of rectum (Dmax0.5cc), as well as meeting existing constraints, resulted in considerable rectal NTCP reductions. Conclusions Boosting DILs in the context of SABR is technically feasible but should be approached with caution. If this therapy is adopted, strict rectal constraints are required including Dmax0.5cc. If the α/β ratio of prostate cancer is 1.5 Gy or less, then high TCP and low NTCP can be achieved by prescribing SABR to the whole prostate, without the need for DIL boosting.


Radiotherapy and Oncology | 2016

Real-time in vivo dosimetry in high dose rate prostate brachytherapy

J. Mason; Arielle Mamo; Bashar Al-Qaisieh; A. Henry; P. Bownes

BACKGROUND AND PURPOSE Single fraction treatments of 15Gy or 19Gy are common in HDR prostate brachytherapy. In vivo dosimetry (IVD) is therefore important to ensure patient safety. This study assesses clinical IVD and investigates error detection thresholds for real-time treatment monitoring. MATERIALS AND METHODS IVD was performed for 40 treatments planned using intra-operative trans-rectal ultrasound (TRUS) with a MOSFET inserted into an additional needle. Post-treatment TRUS images were acquired for 20 patients to assess needle movement. Monte Carlo simulations of treatment plans were performed for 10 patients to assess impact of heterogeneities. Per-needle and total plan uncertainties were estimated and retrospectively applied to the measured data as error detection thresholds. RESULTS The mean measured dose was -6.4% compared to prediction (range +5.1% to -15.2%). Needle movement and heterogeneities accounted for -1.8% and -1.6% of this difference respectively (mean values for the patients analysed). Total plan uncertainty (k=2) ranged from 11% to 17% and per needle uncertainty (k=2) ranged from 18% to 110% (mean 31%). One out of 40 plans and 5% of needles were outside k=2 error detection threshold. CONCLUSIONS IVD showed good agreement with predicted dose within measurement uncertainties, providing reassurance in the accuracy of dose delivery. Thresholds for real-time error detection should be calculated on an individual plan/needle basis.


Radiotherapy and Oncology | 2015

Comparison of focal boost high dose rate prostate brachytherapy optimisation methods

J. Mason; P. Bownes; Brendan Carey; Ann M Henry

For HDR prostate brachytherapy treatments of 15 Gy to the whole gland plus focal boost, optimisation to either tumour plus margin (F-PTV) or involved sectors was compared. For 15 patients median F-PTV D90 and V150 were 21.0 Gy and 77.2% for F-PTV optimisation and 19.8 Gy and 75.6% for sector optimisation.


Brachytherapy | 2014

Multi-parametric MRI-guided focal tumor boost using HDR prostate brachytherapy: A feasibility study

J. Mason; Bashar Al-Qaisieh; P. Bownes; Dan Wilson; David L. Buckley; D.I. Thwaites; Brendan Carey; Ann M. Henry


Brachytherapy | 2014

Investigation of interseed attenuation and tissue composition effects in 125I seed implant prostate brachytherapy

J. Mason; Bashar Al-Qaisieh; P. Bownes; Ann M. Henry; D.I. Thwaites


Radiotherapy and Oncology | 2018

PV-0253: Importance of DCE- MRI for targeting biopsy and salvage treatments after prostate cancer recurrence

J. Mason; E. Adiotomre; B. Carey; P. Bownes; A. Henry


Radiotherapy and Oncology | 2016

OC-0063: Real-time in-vivo dosimetry in HDR prostate brachytherapy

J. Mason; Bashar Al-Qaisieh; A. Henry; P. Bownes


Radiotherapy and Oncology | 2015

OC-0174: Real-time in-vivo dosimetry for HDR prostate brachytherapy

A. Mamo; J. Mason; Bashar Al-Qaisieh; A. Henry; D. Okkalides; P. Bownes


Radiotherapy and Oncology | 2014

PO-1022: Dosimetry modelling for focal high dose rate prostate brachytherapy

J. Mason; Bashar Al-Qaisieh; D.I. Thwaites; P. Bownes; A. Henry


Radiotherapy and Oncology | 2013

PO-0965: Clinical investigation of inter seed attenuation effects in prostate I-125 seed implant brachytherapy

J. Mason; Bashar Al-Qaisieh; P. Bownes; A. Henry; D.I. Thwaites

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P. Bownes

St James's University Hospital

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Bashar Al-Qaisieh

St James's University Hospital

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Ann M. Henry

St James's University Hospital

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Brendan Carey

Leeds Teaching Hospitals NHS Trust

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Ann M Henry

University of Manchester

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B. Carey

St James's University Hospital

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C.M. Thompson

St James's University Hospital

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