J. Mason
University of Leeds
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Publication
Featured researches published by J. Mason.
International Journal of Radiation Oncology Biology Physics | 2014
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
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
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
J. Mason; Bashar Al-Qaisieh; P. Bownes; Dan Wilson; David L. Buckley; D.I. Thwaites; Brendan Carey; Ann M. Henry
Brachytherapy | 2014
J. Mason; Bashar Al-Qaisieh; P. Bownes; Ann M. Henry; D.I. Thwaites
Radiotherapy and Oncology | 2018
J. Mason; E. Adiotomre; B. Carey; P. Bownes; A. Henry
Radiotherapy and Oncology | 2016
J. Mason; Bashar Al-Qaisieh; A. Henry; P. Bownes
Radiotherapy and Oncology | 2015
A. Mamo; J. Mason; Bashar Al-Qaisieh; A. Henry; D. Okkalides; P. Bownes
Radiotherapy and Oncology | 2014
J. Mason; Bashar Al-Qaisieh; D.I. Thwaites; P. Bownes; A. Henry
Radiotherapy and Oncology | 2013
J. Mason; Bashar Al-Qaisieh; P. Bownes; A. Henry; D.I. Thwaites