HPV P16 positive cancer

Posted by frankbc @frankbc, Oct 27, 2020

Hello, I am reaching out to see if anyone in this group is diagnosed with HPV P16 positive cancer We have unknown origin and are being treated for head and neck cancer. Anyone else with similiar presenation?.

Interested in more discussions like this? Go to the Head & Neck Cancer Support Group.

@sandralea58

My husband was diagnosed in August 2022, SCC HPV+ to right tonsil and base of tongue. He underwent 35 rounds of radiation over 6 weeks. He finished treatment Dec 19, 2022. His taste is beginning to return, the wounds on his neck have healed and after a scope yesterday, the doctors are pleased with the results. They believe the treatment has been successful. His PET scan will take place the first week of April to confirm NED. We are so grateful.

Jump to this post

Where did your husband do his treatment? My husband was just diagnosed.

REPLY
@ywallace

Where did your husband do his treatment? My husband was just diagnosed.

Jump to this post

We are in Canada. His treatment was at BC Cancer
Centre in Victoria BC. We have nothing but wonderful things to say about his team. All went like clockwork and we are in the recovery stage. He was offered 3 rounds of Cisplatin, but with only at 1-2% uptick to the 85% positive results they gave him. He is 70 and declined the chemo.

REPLY

I was diagnosed exactly the same in May 2022. Doctors completed exploratory robotic surgery to identify the small group of cells on the base of my tongue and a needle biopsy of the mass in the right side of my neck throat area also came back positive. I completed 7 weeks of radiation and chemo treatments this past summer. I was cancer free in November 2022 based on blood work / NAVDX testing.

REPLY

My HPV+ cancer was diagnosed Nov 2022 when I had a lump on the left side of my neck. Biopsy was inconclusive so had surgery to remove it and came back positive for cancer. Next step was a left modified neck dissection which removed 32 lymph nodes all negative. Had exploratory robotic surgery at the same time which identified the primary tumor in the left tonsil. A month later a full TORS ( trans oral robotic surgery) to perform a radical tonsillectomy and remove tissue from the base of my tongue. That was 5 weeks ago and I’m now exploring options for radiation to my neck and chemo due to the original spread to one lymph node. The surgery was a success and there were clear margins so all the tumor was removed. Also my NavDx blood test came back clear which indicates no tumor remains. I’m back to eating most foods with the help of a speech therapist and looking for the radiation treatment best for my situation that will have the least side effects. Please know that HPV cancer is very responsive to treatment and while the treatments are tough the outcomes are very positive.

REPLY
@smittyfromcuse

My HPV+ cancer was diagnosed Nov 2022 when I had a lump on the left side of my neck. Biopsy was inconclusive so had surgery to remove it and came back positive for cancer. Next step was a left modified neck dissection which removed 32 lymph nodes all negative. Had exploratory robotic surgery at the same time which identified the primary tumor in the left tonsil. A month later a full TORS ( trans oral robotic surgery) to perform a radical tonsillectomy and remove tissue from the base of my tongue. That was 5 weeks ago and I’m now exploring options for radiation to my neck and chemo due to the original spread to one lymph node. The surgery was a success and there were clear margins so all the tumor was removed. Also my NavDx blood test came back clear which indicates no tumor remains. I’m back to eating most foods with the help of a speech therapist and looking for the radiation treatment best for my situation that will have the least side effects. Please know that HPV cancer is very responsive to treatment and while the treatments are tough the outcomes are very positive.

Jump to this post

It is amazing how many people have very similar issues to mine. Throat cancer to radiation/chemo to neck dissection to throat damage from radiation to feeding tube to recovery to ongoing treatment. It is helpful to know that others have gone through it so there s a process and experience. My cancer is chronic, but your testimonies keep me positive.

REPLY

My tongue cancer was caused by HPV16. My recommended treatment is chemo therapy and 35 radiation treatments. I had my first chemo treatment yesterday. I had my radiation mask made covering my head down to shoulders. This was the worst thing that's happened to me since being diagnosed with tongue cancer. I have claustrophobia and I started freaking out. Near the end of the mask run through I started trying to get the mask and mouthpiece out and calling for help. Finally that was over only to be told I had to do this one more time. I explained about my fear to the nurse who basically said nothing can be done just do it. Since my treatments will probably start in two weeks I have made requests for a sedating drug such as valium. I was flatly turned down and said it's only 5 minutes deal with it. I can tell you after that 1st day (yesterday) I was physically shaking and could barely walk. Unfortunately this was the one day I did not come with my husband. I am dreading my next radiation treatment. Did anyone out there have similar experiences and if so what did you do?

REPLY
@anybody10

My tongue cancer was caused by HPV16. My recommended treatment is chemo therapy and 35 radiation treatments. I had my first chemo treatment yesterday. I had my radiation mask made covering my head down to shoulders. This was the worst thing that's happened to me since being diagnosed with tongue cancer. I have claustrophobia and I started freaking out. Near the end of the mask run through I started trying to get the mask and mouthpiece out and calling for help. Finally that was over only to be told I had to do this one more time. I explained about my fear to the nurse who basically said nothing can be done just do it. Since my treatments will probably start in two weeks I have made requests for a sedating drug such as valium. I was flatly turned down and said it's only 5 minutes deal with it. I can tell you after that 1st day (yesterday) I was physically shaking and could barely walk. Unfortunately this was the one day I did not come with my husband. I am dreading my next radiation treatment. Did anyone out there have similar experiences and if so what did you do?

Jump to this post

Hi. I went through the same treatment. Fortunately for me I’m not claustrophobic. I can tell you that the treatment did last only about 5-7 minutes and the table does shift slightly to give the radiation the exact location where to concentrate the waves. Amazed that they won’t prescribe something as I have heard other patients have been. I pray that you get something to aid you and wish you the best.

REPLY
@anybody10

My tongue cancer was caused by HPV16. My recommended treatment is chemo therapy and 35 radiation treatments. I had my first chemo treatment yesterday. I had my radiation mask made covering my head down to shoulders. This was the worst thing that's happened to me since being diagnosed with tongue cancer. I have claustrophobia and I started freaking out. Near the end of the mask run through I started trying to get the mask and mouthpiece out and calling for help. Finally that was over only to be told I had to do this one more time. I explained about my fear to the nurse who basically said nothing can be done just do it. Since my treatments will probably start in two weeks I have made requests for a sedating drug such as valium. I was flatly turned down and said it's only 5 minutes deal with it. I can tell you after that 1st day (yesterday) I was physically shaking and could barely walk. Unfortunately this was the one day I did not come with my husband. I am dreading my next radiation treatment. Did anyone out there have similar experiences and if so what did you do?

Jump to this post

Many of us have gone through this.
Though I’m not claustrophobic I don’t like being held down but here’s the thing; relax, keep positive thoughts, be convinced that there is no other option and confident that this procedure will kill that crap!
Don’t know what your beliefs are but I prayed for comfort to be upon you!

MOJO

REPLY

Thar's great advice. I asked them to pipe in music that I liked so i could think about something else. I just focused on my breathing. Keep it steady and relaxed.

REPLY
@chamst

I just got diagnosed with this type of cancer. Am yet to start treatment but am told it will be Cisplastin (Chemo) and targeted radiation for 7 weeks. My mum had a very similar cancer treated the same way a couple of years ago. She has had significant damage done by the radiation and now cannot keep her weight up, even two years later. I would like to suggest a lower dose of radiation since this P16+ responds so well to radiation anyway. I'm hoping the radiology oncologist will agree...

Jump to this post

I was diagnosed with HPV16 tongue cancer in November 2021. I've just started treatments and feel better already. I'm told that it does get worse before it's better but that will remain to be seen. I've had 2 chemo treatments and 5 radiation treatments. I dislike the radiation treatments enormously because of my claustrophobia. The mask was made and it bolts my head and shoulders down on the rad. table. Then of course you get prompts about swallowing or not swallowing. Of course my body reacts in the opposite so swallow when I'm not supposed to. I've sort of tamed the fear of being bolted down but not completely. I usually have 2 days out of the week that I feel bad from the chemo treatment. It's a little frightening reading here about others experiences with radiation and the lingering effects. Are there ever any good outcomes?

REPLY
Please sign in or register to post a reply.