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Hello everyone! I got a call from my ENT today. He had forwarded my cat scan to my surgeon at Virginia Mason in Seattle so he could review & bring before tumor board. They want pet scan done for a base line for future comparisons if needed & just to be sure everything is clear like they suspect. As I understand it, pet scans give a lot of false postives. Does that mean a negative would be really good? I'm concerned that if we get false negatives, then here we go with biopsies & all the garbage that goes with it; freak out, worry, despair, healing from the biopsy, etc., etc. I've just had about enough of this freakin disease!!! Can somebody just make it all go away?


dx 2/11/04 scca bot T3 IU 2B MO poorly differentiated, margins ok, 3/16 modest, jaw split, over half of tongue removed, free flap from left forearm - finished chemo & rad treatment 5/20/04
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I added this to a post in another section on this topic.

For those of you who are medical term impaired or confused:

A "positive" result in a biopsy (or any other medical test or scan result) means that you have tested positive (or have a highly suspicious area) for whatever they were testing or looking for, e.g. cancer, squamous cell carcinoma, etc.

Conversely a "negative" result means that you don't have what they were testing for.

So a false positive may result in additional and unwarranted testing and procedures. A false negative means the condition they are looking for is missed, when it is in fact, present.

These guys (the radiologists and ENT's) are usually smart enough to discern a false positive from an ROI (region of interest). For instance, they know that scar tissue can light up on a PET. They will typically order an in depth "visualization" of the area (which they are probably already doing.

Consider yourself fortunate that they are doing this - many of us can't get our HMO's to order a PET scan. I went to UCSFCCC and they only followup with annual MRI's and chect X-rays (which is great if I have a recurrence at the original site). A PET will show up distant metastesis before it's untreatable, such as liver or lung nodules. By the way PET/CT's are very accurate, if you can get one of those.

I hate to say it but "freak out, worry and despair" and part of the cancer game. That's why we call it the club that no one wants to join. It gets better though as time goes on.


Gary Allsebrook
***********************************
Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2
Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy)
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"You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
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Erik,

I am sorry to see you going through these difficult times. It seems like about the same time you stop thinking about it, something pops up that churns you through the cycle again. Hopefully it is nothing to worry about and the doctors are just being cautious because they know how mean the beast can be.

I had a PET/CT two months after treatment for a baseline. I have since had one at 6 months and one at a year. There were three ROI's (regions of interests) on the first scan and they were certain it was only scar tissue since they all three were in the most intensely radiated areas, one being the primary tumor site. The second and third scans were compared to the first to determine any differences in area to evaluate growth in the three regions. My ENT and the radiologist and the medical oncologist and the radiation oncologist all read the scans and concur there has been no growth although they will continue to monitor at 6 months for precautionary reasons. They all agree that the PET/CT is by far the most accurate test and even offer the entire scan on CD (for a mere $15) to send to anyone I wish for a second opinion.

I was fortunate because I am allergic to CT contrast so my insurance had no options other than PET and the only PET facility my doctors use only provides PET/CT scans. They cost over $6,000 each. Ironically, the insurance company pays this but won't pay for having some questionable teeth pulled.

False negatives are the least likely result of a PET/CT and false positives are the reason they will do multiples over a span of time to use the first as a baseline for comparative purposes. In the meantime, try to not worry and if you lose sleep, work on just the night before the scans. I wish I could make it all go away for all of us but unfortunately it is now an integral part of our lives. It sucks.

Ed


SCC Stage IV, BOT, T2N2bM0
Cisplatin/5FU x 3, 40 days radiation
Diagnosis 07/21/03 tx completed 10/08/03
Post Radiation Lower Motor Neuron Syndrome 3/08.
Cervical Spinal Stenosis 01/11
Cervical Myelitis 09/12
Thoracic Paraplegia 10/12
Dysautonomia 11/12
Hospice care 09/12-01/13.
COPD 01/14
Intermittent CHF 6/15
Feeding tube NPO 03/16
VFI 12/2016
ORN 12/2017
Cardiac Event 06/2018
Bilateral VFI 01/2021
Thoracotomy Bilobectomy 01/2022
Bilateral VFI 05/2022
Total Laryngectomy 01/2023
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Gary, I am in no way impaired or confused other than my ability to swallow & speak & maybe proof read! I meant false positive in regards to my concerns.


dx 2/11/04 scca bot T3 IU 2B MO poorly differentiated, margins ok, 3/16 modest, jaw split, over half of tongue removed, free flap from left forearm - finished chemo & rad treatment 5/20/04
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That wasn't meant to be anything personal - it was my feeble attempt to be funny. But I have to admit sometimes it's difficult for many to figure out what "positive" and "negative" means from a medical perspective since they have opposite meanings from what normal people are used to and are are confused here when discussing it. Then add the word "false" to it and it compounds the confusion issue.

I have to admit that I WAS in fact impaired for a fair amount of time post Tx. My wife told me I had a difficult time comprehending complex issues and also focusing on things so that's ok too. The Tx beats the hell out you! I'm glad you're doing well - you're the exception!


Gary Allsebrook
***********************************
Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2
Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy)
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Talk about impaired. During treatment I swore I was doing just fine mentally when a store clerk I know sent me to the store restroom to put my blouse on right side out (grin). My husband wouldn't play Scrabble with me either. And a friend still laughs at how I couldn't open the window I mistook for the door in a restaurant. I do NOT miss those days.

Erik, it will get better. I promise!

Edited to say I do not mean you are confused, Erik, just that the father out you are, the better you will feel and the less you will worry. You are still pretty close, relatively speaking, from end of treatment. Six months and a year from now you will look at things diffently, I am sure.

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Doctor speak is perplexing. The way the use the negatives/positives, indicated, remarkable, etc. I wonder how many hours of classes they spend on changing the lexicon to set them apart in all discussions eek .

Ed


SCC Stage IV, BOT, T2N2bM0
Cisplatin/5FU x 3, 40 days radiation
Diagnosis 07/21/03 tx completed 10/08/03
Post Radiation Lower Motor Neuron Syndrome 3/08.
Cervical Spinal Stenosis 01/11
Cervical Myelitis 09/12
Thoracic Paraplegia 10/12
Dysautonomia 11/12
Hospice care 09/12-01/13.
COPD 01/14
Intermittent CHF 6/15
Feeding tube NPO 03/16
VFI 12/2016
ORN 12/2017
Cardiac Event 06/2018
Bilateral VFI 01/2021
Thoracotomy Bilobectomy 01/2022
Bilateral VFI 05/2022
Total Laryngectomy 01/2023
Joined: Nov 2002
Posts: 3,552
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Surprisingly similar to lawyer speak. Plus they make up words and terms. I remember reading an article many years ago in "Radiology Today" about a condition called "Gosepyboma" AKA the "problem of the retained surgical sponge" (OOPS eek ) Apparently quite often fatal. They are supposed to count them so that none are left behind (they are now required to put radiographic markers on them so they show up in x-rays). They also leave other surgical instruments behind as well. :p

Plus they have sublanguages. Many radiological terms are not found in the medical encyclopedias like Tabers.

It is a art - not a science :rolleyes:


Gary Allsebrook
***********************************
Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2
Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy)
________________________________________________________
"You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
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Hi Erik,

Thought I would add my 2 cents on this one. I just saw my surgeon about one week ago for a routine follow up. I had a CT about three weeks prior to that. My radiation oncologist (whom I had seen about two months earlier) wanted me to ask my surgeon about a pet scan, so I did. Here is my surgeon's opinion (for what it's worth). He feels it's the 'new toy' that a lot of people are now using. He said we can certainly do a pet scan (my local CA center has a pet scanner), but he said with all of the false positives, he wouldn't want to put me through that. He further said (and this really resonated with me) that at present there simply is no good long term clinical data to support its use (in his opinion). This is at odds with my radiation oncologist, who strongly implied that it would be a very good idea to consider adding it to my follow up regimen. Who knows?? Best of luck to you.

David


Stage 1 lateral border of tongue in 1986 requiring L neck dissection, three surgeries later in Feb 2004 invasive SCC (poorly differentiated) L radical neck dissection followed by 37 treatments XRT
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The medical professionals that use PET like them and the ones that don't, give you the false + line. Mine was right on and found cancer in both lungs. This was not picked up by the standard one year x-ray 4 months earlier. I would be much farther along on the road to death without the PET, and I know I am not alone here. If you can find a facility that knows how to read one, and your insurance will pay, get one. I had mine at MSKCC and they seem very confident in their results. The real disappointment for me came, not from finding the cancer but from learning that I did not have one of the often referred to false positives. I would be curious to see how many of us have had a confirmed false reading of a PET scan.

Glenn

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