First Time Posting and CEA Markers
I look forward to sharing our "roller coaster ride" with everyone. Some of our experiences sound similar to the ones shared here, some seem a little different and we have had at least one experience that has not been mentioned here at all and is relatively new to the market.
Our family is about 16 months into this "roller coaster ride" and my anxiety level is growing. I read one of Mr. Marshall's posts awhile back and he said "maybe they are not telling you the whole story" and that has stuck with me. I think my mom and dad tell me what they want me to hear. Mr. Marshall, you have 8 years experience here on the site and you have seen many come and go and I think your wealth of personal knowledge is worth more than many of the statistics/stories I see out there. If I read you correct and please correct me if I am wrong (and I would like to be wrong) it seems here on this site 24 months survival for a Stage IVB is about average. Is that correct?
I think you know where I am going, so here is my question. Not a lot is said on this site about CEA Markers. Since my dad started chemo treatment every time he has a blood draw, which has been about three times a month, he gets his CEA Marker. He started around 45, it went down to 3 and now is up over 600. So, I would like to know what the CEA Markers are for other family members here are. I cannot find anywhere (anything believable anyway) how high this number can go. Could someone please shed some light for me or at least your own experiences?
My mom says don't pay too much attention to the number as it doesn't always correlate to what is going on, Pet/Ct scans are the best. And yes, one time this was true but ever since as the CEA number goes up, the pet/ct scans get worse.
I cannot post often right now but I will in time, and thank you in advance for all of your feedback!
Comments
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CEA Markers
I haven't heard of CEA markers per say but my wife had colon cancer a couple of years ago and one of the things they track with a blood test is CEA. I'm going from memory now, but CEA is a protein that is only normally found in fetuses. It's a growth thing. As we get older the levels of CEA in our blood diminishes to where average count for a 50 y/o male should be less than 5. When my wife had cancer her's were elevated up to over 100 but since her surgery has been on a staedy decline. She is at .125 now. Don't know if this sheds any light or not but you can Google CEA Protein and gather some more info. Again, not really sure what this means as far as Esophaegal cancer is concerned. This link might be helpful:
http://www.medterms.com/script/main/art.asp?articlekey=8722
Michael Daniels
Brandon, FL0 -
This comment has been removed by the ModeratorCallaloo said:Not relevant to EC
I don't know what your mom's numbers mean, but I've been told by my doctors that tumor markers are not relevant to esophageal cancer. I've been tested for CA markers for other cancers in the past, but never for EC.0 -
This comment has been removed by the ModeratorCallaloo said:Not relevant to EC
I don't know what your mom's numbers mean, but I've been told by my doctors that tumor markers are not relevant to esophageal cancer. I've been tested for CA markers for other cancers in the past, but never for EC.0
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