Cetuximab and Radiation
This is my first post, primarily because I have not found a kindred spirit on this discussion board. On February 26, I had a cancerous (SCC) removed from my cheek. It was not in the parotid gland, but near the duct. There was no evidence of a primary source The tumor was sitting on the facial muscle, and was discreet. Three different doctors thought it was a cyst. The fourth did a FNB,and then ordered a CAT scan Feb.23, diagnosed Feb. 25, removed Feb. 26. my surgeon was phenomenal. No injury to facial nerve or muscle. Six weeks later I began cetuximab weekly for 6 weeks, while concurrently receiving 30 radiation treatments. Side effects for Cetuximab: horrendous rash which eventually had to be treated by a dermatologist. Two weeks after Cetuximab treatment has ended, the rash is resolving. I am having more difficulty with the side effects of the radiation. Sore tongue, dry mouth, mucous. I cannot tolerate the lack of taste, so my diet is protein shakes. Nevertheless, I would definitely do the Cetuximab, and the radiation. Aggressive action is necessary to defeat the beast.
Comments
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it just takes time
Nonni1947,
Welcome to the H&N forum, where many of us have used Erbitux.
I was stage IVa, scc, bot, 1 lymph node, hpv+ (surgery, rads & Erbitux). Yes, the side effects of Erbitux clear up quickly, but that darn radiation is a persistent pain in the a _ _. It took me many months for my “new normal” to include semi-normal eating.
If you follow a similar path you will have a happy food future, which might include roasting hot dogs, like I am going to do RIGHT NOW!
Good luck,
Matt
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