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The degrees of freedom is a little bit of a red herring and an unartful description by me.does not quite have infinite degrees of freedom
The point I was trying to make is that the dosimetry of photon treatment is sound enough that you can quickly run through a nearly infinite number of permutations to find optimal dosimetric solutions utilizing many gantry positions (quite a few if arc based plans) and dynamic and complicated modulation of the beam.
This is because the energy deposition and biologic impact of the beam is pretty well defined as is the impact of physical beam modulation. (Not to say there aren't little bits of magic that can happen with photon treatment, including out of beam effects).
While I understand that there is another degree of modulation along the beam axis for protons, the fact that the biologic effect of simple beam arrangements is not readily calculable in year 2020 is shocking. In the paper I referenced, the dose profile would seem close to identical to the physician reviewing a dose only representation of the plans made by flat vs downslope opposed fields, however the LET profile across those fields is very different and the LET-RBE relationship is not well modeled by contemporary methods.
There is no doubt that the physics of protons is cool. But when LET profiles varying as much as 150% in some places are giving you the same dose representation, somethings not right IMO. Then add to it that the LET to cell kill numbers in vitro are not well understood and I'm getting nervous.
Unless it can be better explained to me, I stick by the suspicion that the clinical benefit of the proton approach will be limited to those scenarios where one is far away from catastrophic dose ceilings for small hotspots (the hot spot in the serial organ scenario) and where the long term consequences of low dose scatter are clinically meaningful.
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