48 research outputs found

    Monte-Carlo-computed dose, kerma and fluence distributions in heterogeneous slab geometries irradiated by small megavoltage photon fields

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    Small-field dosimetry is central to the planning and delivery of radiotherapy to patients with cancer. Small-field dosimetry is beset by complex issues, such as loss of charged-particle equilibrium (CPE), source occlusion and electron scattering effects in low-density tissues. The purpose of the present research was to elucidate the fundamental physics of small fields through the computation of absorbed dose, kerma and fluence distributions in heterogeneous media using the Monte-Carlo method. Absorbed dose and kerma were computed using the DOSRZnrc Monte-Carlo (MC) user-code for beams with square field sizes ranging from 0.25 × 0.25 to 7× 7 cm2 (for 6 MV \u27full linac\u27 geometry) and 0.25 × 0.25 to 16 × 16 cm2 (for 15 MV \u27full linac\u27 geometry). In the bone inhomogeneity the dose increases (vs. homogeneous water) for field sizes \u3c 1 × 1 cm2 at 6 MV and ≤ 3 × 3 cm2 at 15 MV and decreases (vs. homogeneous water) for field sizes ≥ 3 × 3 cm2 at 6 MV and ≥ 5 × 5 cm2 at 15 MV. In the lung inhomogeneity there is negligible decrease in dose compared to in uniform water for field sizes \u3e 5 × 5 cm2 at 6 MV and ≥ 16 × 16 cm2 at 15 MV, consistent with the Fano theorem. The near-unity value of the absorbed-dose to collision-kerma ratio, D/Kcol, at the centre of the bone and lung slabs in the heterogeneous phantom demonstrated that CPE is achieved in bone for field sizes \u3e 1 × 1 cm2 at 6 MV and \u3e 5 × 5 cm2 at 15 MV; CPE is achieved in lung at field sizes \u3e 5 × 5 cm2 at 6 MV and ≥ 16 × 16 cm2 at 15 MV. Electron-fluence perturbation factors for the 0.25 × 0.25 cm2 field were 1.231 and 1.403 for bone-to-water and 0.454 and 0.333 for lung-to-water were at 6 and 15 MV respectively. For field sizes large enough for quasi-CPE, the MC-derived dose-perturbation factors, lung-to-water, were close to unity; electron-fluence perturbation factors, lung-to-water, were ~1.0, consistent with the \u27Fano\u27 theorem. At 15 MV in the lung inhomogeneity the magnitude and also the \u27shape\u27 of the primary electron-fluence spectrum differed significantly from that in water. Beam penumbrae relative to water were narrower in the bone inhomogeneity and broader in the lung inhomogeneity for all field sizes

    Doxycycline for Malaria Chemoprophylaxis and Treatment: Report from the CDC Expert Meeting on Malaria Chemoprophylaxis

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    Doxycycline, a synthetically derived tetracycline, is a partially efficacious causal prophylactic (liver stage of Plasmodium) drug and a slow acting blood schizontocidal agent highly effective for the prevention of malaria. When used in conjunction with a fast acting schizontocidal agent, it is also highly effective for malaria treatment. Doxycycline is especially useful as a prophylaxis in areas with chloroquine and multidrug-resistant Plasmodium falciparum malaria. Although not recommended for pregnant women and children < 8 years of age, severe adverse events are rarely reported for doxycycline. This report examines the evidence behind current recommendations for the use of doxycycline for malaria and summarizes the available literature on its safety and tolerability

    (Radio)Biological Optimization of External-Beam Radiotherapy

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    “Biological optimization” (BIOP) means planning treatments using (radio)biological criteria and models, that is, tumour control probability and normal-tissue complication probability. Four different levels of BIOP are identified: Level I is “isotoxic” individualization of prescription dose at fixed fraction number. is varied to keep the NTCP of the organ at risk constant. Significant improvements in local control are expected for non-small-cell lung tumours. Level II involves the determination of an individualized isotoxic combination of and fractionation scheme. This approach is appropriate for “parallel” OARs (lung, parotids). Examples are given using our BioSuite software. Hypofractionated SABR for early-stage NSCLC is effectively Level-II BIOP. Level-III BIOP uses radiobiological functions as part of the inverse planning of IMRT, for example, maximizing TCP whilst not exceeding a given NTCP. This results in non-uniform target doses. The NTCP model parameters (reflecting tissue “architecture”) drive the optimizer to emphasize different regions of the DVH, for example, penalising high doses for quasi-serial OARs such as rectum. Level-IV BIOP adds functional imaging information, for example, hypoxia or clonogen location, to Level III; examples are given of our prostate “dose painting” protocol, BioProp. The limitations of and uncertainties inherent in the radiobiological models are emphasized

    Comment on “Simulating Radiotherapy Effect in High-Grade Glioma by Using Diffusive Modeling and Brain Atlases”

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    This paper focuses on the dialectic between the search for truth, adversarial procedure, and lay participation in the preparation, presentation, and evaluation of evidence in criminal trials. Its primary focus is on the reintroduction of trial by jury in two classic inquisitorial criminal justice systems, Russia (1993) and Spain (1995), as a catalyst in those countries’ move to adversary procedure. It focuses on the effect of the jury system on preparing evidence for trial, the presentation of evidence at trial, and the evaluation of evidence

    Fundamentals of ionizing radiation dosimetry

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    The textbook "Fundamentals of Ionizing Radition Dosimetry" bundled with the workbook containing solutions to the exercises is the perfect pair for anyone seriously interested in radiation dosimetry
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