Newly diagnosed Anal cancer patient
Hello all,
I was diagnosed with anal cancer a week ago. I habe an MRI on July 4 and a lymph node biopsy on the 8th. im wondering about the side effects of chemo. Also did anyone get mouth sores, if so, how did you manage them? Those are one of my fears.
Comments
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Newly Diagnosed Anal Cancer Patient
Chemo and radiation both cause side effects, but not everyone gets the same side effects, or gets them to the same degree. I didn't get mouth sores; however my chemo was Capeceitabine
Xeloda) which is 5FU in pill form; therefore I didn't have a fanny pack. One day one, I did get an infusion of mitomycin and began the pills and radiation; I didn't get the one day of mitomycin the last week along with the Xeloda. (I'm not sure why)
For anal cance the chemo is a radiosensitizer that enhances the effect of the radiation. The radiation is what is critical .
NCCN(National Comprehensive Cancer Network...an organization representling a group of comprehensive cancer centers) and the Analcancerfoundation has just issued an excellent booklet for patients . ncccn.org is free, but you may have to create an account. I am unable to attach a pdf of this booklet to my comment section. I am 6 years out from treatment and wish this booklet had been available for patients when I was diagnosed. It is comprehensive and contains the latest recommendations that oncologists follow in treating this cancer. If you are unable to access this site, please let me know and I will find another way for you to access it.
https://www.nccn.org/patients/guidelines/content/PDF/anal-patient.pdf
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Newly Diagnosedtanda said:Newly Diagnosed Anal Cancer Patient
Chemo and radiation both cause side effects, but not everyone gets the same side effects, or gets them to the same degree. I didn't get mouth sores; however my chemo was Capeceitabine
Xeloda) which is 5FU in pill form; therefore I didn't have a fanny pack. One day one, I did get an infusion of mitomycin and began the pills and radiation; I didn't get the one day of mitomycin the last week along with the Xeloda. (I'm not sure why)
For anal cance the chemo is a radiosensitizer that enhances the effect of the radiation. The radiation is what is critical .
NCCN(National Comprehensive Cancer Network...an organization representling a group of comprehensive cancer centers) and the Analcancerfoundation has just issued an excellent booklet for patients . ncccn.org is free, but you may have to create an account. I am unable to attach a pdf of this booklet to my comment section. I am 6 years out from treatment and wish this booklet had been available for patients when I was diagnosed. It is comprehensive and contains the latest recommendations that oncologists follow in treating this cancer. If you are unable to access this site, please let me know and I will find another way for you to access it.
https://www.nccn.org/patients/guidelines/content/PDF/anal-patient.pdf
I had mouth sores. The mourthwash that everyone talks about was not covered by my insurance and would have cost > $100. I was stubborn and thought I could endure it. I recall trying to eat a hard taco and it felt like knives were cutting my mouth. Anyway.. I really had little of an appetite. It turnedout that the NP at my oncologist's office had samples of something that helped but meanwhile my daughter had picked up something at the drugstore that did help somewhat. Don't hesitate to reach out to your medical team and mention any problems.
I recall being more concerned about the side effects of the radiation and I don't recall any real problems related to that (except for some itching especially at night).
Just keep your eye on the end result of the treatment.
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