I'm not super familiar with computer graphics, so you'll have to let me know if my description fits what you guys do ;)
I found a youtube video (https://www.youtube.com/watch?v=msX1ypCjkK4) that should give you an idea of what I'm describing actually looks like. Specifically it introduces the concept of a multi-leaf collimator which serves as the main collimating device in modern radiotherapy. The other degree of freedom is the angle of the gantry you see rotating around the patient.
Typically for every gantry angle, the treatment planning software would split up an open field (no collimation) into a bunch of 1x1 cm^2 "beamlets" and would simulate what kind of dose distribution you would get inside the patient from each beamlet (you turn the patient CT into a big 3D grid of voxels to simulate dose in).
You then throw all those dose distributions into an optimiser, and you do what's called a fluence map optimisation which gives you the amount of radiation you want to deliver out of each beamlet. This is the optimisation step I described earlier where the cost function is basically a square difference between the dose in each organ from a given set of beamlet weights and what you want the dose to actually be. Healthy tissue is the limiting factor so you give as much as you can to the tumour while making sure that less than X% of the volume of a nearby organ gets more than Y units of radiation. There's a final step at the end that turns the fluence maps into actual deliverable apertures shaped by the multi leaf collimator.
There's a huge amount of work that goes into the simulation aspect. You can't just model the radiation beam as pure light sources that attenuate in the body via some exponential decay because the high energy photons scatter off electrons which themselves scatter around while depositing energy (radiation dose) away from the point of interaction. The gold standard is Monte Carlo simulations (which is my area of research) since you can model the actual physics of particle transport but in practice most clinics will use a faster engine to generate dose distributions. The faster engines typically superpose a primary component (a pure exponential decay) convolved with a kernel representing the energy that gets deposited away from the point of interaction.
That's probably way more information than you wanted ;)
Wow, that video is really cool! The sliding lock-tumbler mechanism offers a really interesting amount of control over the aperture shaping the beam! Sort of like a brush in photoshop!
I found a youtube video (https://www.youtube.com/watch?v=msX1ypCjkK4) that should give you an idea of what I'm describing actually looks like. Specifically it introduces the concept of a multi-leaf collimator which serves as the main collimating device in modern radiotherapy. The other degree of freedom is the angle of the gantry you see rotating around the patient.
Typically for every gantry angle, the treatment planning software would split up an open field (no collimation) into a bunch of 1x1 cm^2 "beamlets" and would simulate what kind of dose distribution you would get inside the patient from each beamlet (you turn the patient CT into a big 3D grid of voxels to simulate dose in).
You then throw all those dose distributions into an optimiser, and you do what's called a fluence map optimisation which gives you the amount of radiation you want to deliver out of each beamlet. This is the optimisation step I described earlier where the cost function is basically a square difference between the dose in each organ from a given set of beamlet weights and what you want the dose to actually be. Healthy tissue is the limiting factor so you give as much as you can to the tumour while making sure that less than X% of the volume of a nearby organ gets more than Y units of radiation. There's a final step at the end that turns the fluence maps into actual deliverable apertures shaped by the multi leaf collimator.
There's a huge amount of work that goes into the simulation aspect. You can't just model the radiation beam as pure light sources that attenuate in the body via some exponential decay because the high energy photons scatter off electrons which themselves scatter around while depositing energy (radiation dose) away from the point of interaction. The gold standard is Monte Carlo simulations (which is my area of research) since you can model the actual physics of particle transport but in practice most clinics will use a faster engine to generate dose distributions. The faster engines typically superpose a primary component (a pure exponential decay) convolved with a kernel representing the energy that gets deposited away from the point of interaction.
That's probably way more information than you wanted ;)