- Joined
- Apr 16, 2004
- Messages
- 4,661
- Reaction score
- 5,080
I've been following a middle-aged female for about 2 years with a large, diffuse, unresectable grade II oligodendroglioma (1p19q non co-deleted). Initial presenting symptoms were partial seizures. She was placed on anti-epileptics and temozolomide. After one year of chemo, no change in tumor on imaging so temozolomide was discontinued.
Now one year later she presented with breakthrough seizures and diplopia. These symptoms were mostly resolved with Decadron and a second anti-epileptic. Tumor board is now recommending salvage radiation. The treatment volumes are too damn big to seriously consider anything other than opposed tangents or a simple 3D plan.
The question is how high I should go in dose? Right now I'm thinking about 50.4 Gy in 28 fractions but am concerned about giving this much radiation to the entire supratentorial area. Unfortunately, there is no clear area to boost and none of the tumor is enhancing. I've prescribed her Namenda to preserve what I can of her future neuro-cognitive function.
Now one year later she presented with breakthrough seizures and diplopia. These symptoms were mostly resolved with Decadron and a second anti-epileptic. Tumor board is now recommending salvage radiation. The treatment volumes are too damn big to seriously consider anything other than opposed tangents or a simple 3D plan.
The question is how high I should go in dose? Right now I'm thinking about 50.4 Gy in 28 fractions but am concerned about giving this much radiation to the entire supratentorial area. Unfortunately, there is no clear area to boost and none of the tumor is enhancing. I've prescribed her Namenda to preserve what I can of her future neuro-cognitive function.