Tonsil Cancer from HPV: Anyone else?
I discovered I had a tumor on my right tonsil in April and it had moved to one lymph node - I had robotic surgery at mayo and had both tonsils removed - all pathology showed all cancer removed from tonsil after surgery -I had the affected Lymph node along w 40 other lymph nodes removed - thank goodness none of the other lymph nodes were positive for cancer.
I have had 2 blood tests since surgery for HPV both negative I will repeat in 2 months - have had another Ct all good— the 2nd PET scan showed something near surgery site— my surgeon said all ok - just inflammation- am worried about that -
I am not doing radiation or chemotherapy unless something changes-I keep reading that most people have radiation
Just wondering if others have had this w no radiation- one more question- my taste buds r really messed up my mouth is very dry - it’s only been a little over 4 months - just interested to hear other’s experiences- thank you
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Thank you Jones. I think I want to put my attention on how successful the treatment is instead of the side effects. I have small children and one is afraid to leave them behind. I need advices to stay positive for the treatment. Thank you so much for your support
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2 ReactionsHi. I had Stage IV tonsil cancer in 2008. Both tonsils were removed, then 33 radiation and 6 chemo. I never learned if it was HPV or other caused, but I still here! The path will be challenging, but you can make it.
If you have a feeding tube, be sure to use it if/when needed to keep your calorie count and hydration level up.
Best wishes
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6 ReactionsThank you very much for the words of encouragement.
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1 ReactionBut you didn’t experience any recurrence?
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1 ReactionNo recurrence. I do see my surgeon 1x per year, have annual chest CT and thyroid ultrasound.
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1 ReactionHi @linda90,
In 2008 I was officially Stage IVB T2N3M0 on left tonsil caused by HPV and one of my 3 infected lymph nodes was over 7cm and that is not a typo. I had 35 rounds (7 weeks) of Photon radiation which amounted to 70 Gy and 3 rounds of the platinum-based chemo Cisplatin and had no surgery whatsoever. In addition, cancer free in March of 2009.
Unfortunately, I was diagnosed with Tongue cancer on my left side of my mouth on March 1, 2024, and had a left partial glossectomy with a radical forearm free flap surgery on April 3, 2024. It also included a modified radical neck dissection. This one was not caused by HPV and was most likely from too much radiation from the first cancer as it is literally adjacent to my left tonsil.
One thing I am finding out is this big de-escalation Head & Neck cancer treatments coming about especially for people who got it as a result of HPV. I attached some articles on it here. Thus, I would push for the Proton radiation as @jonesja mentioned in the prior comments so you could have a better quality of life afterwards with less of the side effects.
Good luck on your journey.
Low-Dose Radiation To Treat HPV Throat Cancer a 'Game Change' 02-12-24 (Low-Dose-Radiation-To-Treat-HPV-Throat-Cancer-a-Game-Change-02-12-24.pdf)
Less Treatment for HPV-Related Oropharyngeal Cancer - NCI article 09_27_23 (Less-Treatment-for-HPV-Related-Oropharyngeal-Cancer-NCI-article-09_27_23.pdf)
De-Escalated Treatment for HPV Related Oropharyngeal Cancer_05-24 article (De-Escalated-Treatment-for-HPV-Related-Oropharyngeal-Cancer_05-24-article.pdf)
In the Office with Dr (In-the-Office-with-Dr.-Marshall-Posner-on-Head-an-Neck-HPV-Cancer-article.pdf)
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5 ReactionsI was diagnosed in May, started radiation & cisplatin in July, completed 30 radiations over 6 weeks and 6 cisplatin treatments( I opted out of last week). Make sure they did a blood HPV test before starting treatment( Naveris) and following completion of treatment blood DNA should be undetectable which strongly supports curative therapy.
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4 ReactionsYou didn’t have chemotherapy? Because they suggested 35 sessions of radiotherapy and one chemotherapy after the third week.
Hi Linda,
In June 2024 I completed 35 rounds of radiation and 6 chemo for stage 3 HPV related tonsil cancer. The treatment was somewhat challenging as I'm sure you've gathered by now from others in this forum but definitely tolerable and more important survivable. As I've mentioned a few times since joining this group, one area where I differ from some others is I am a big proponent of having a feeding tube inserted. My team insisted and I'm grateful they did. It helped maintain my nutritional needs and now I have nothing but a very small scar to show for it. I had the "button" type which is smaller and very easy to use and maintain. Bottom line, a little more than a year post treatment I'm about 95% my old self enjoying life everyday. Best of luck, there is quality of life after this.
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2 ReactionsThank you for these links. This is exactly the treatment I am hoping for.
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