CA 27-29 numbers rising: Does anyone else have an issue like this?

Posted by sandyjr @sandyjr, Jul 1, 2019

My Ca 27.29 seems to be high....in the 40’s....and my oncologist says that that is probably normal for me. He checked the records from my first bc. Does anyone else have an issue like this?

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I don’t understand how breast massage is helpful-thx so much for sharing but could you elaborate? Xo

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@windyshores

My oncologist doesn't do these blood markers at all. I am 9 years out and stopped letrozole at 5 years. I have no idea how I will know I am stage 4. How many of you have docs who do this testing?

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Signatera liquid blood tests can help ease your mind and give you a heads up if BC is coming back. Medicare pays for this.

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@keepmoving2

Hi all - circling back on what is a thread that started in 2019 about rising tumor markers & morphed slightly about good diet, exercise & staying on top on things. It just popped back into my feed by a “like” & it reminded me that it is all still relevant. And stories change.

In July 2024 I will be 5 years in with Stage 4 breast cancer & yes now Stage 4 Mallarian (reproductive) cancer that we did not know I had until a growing brain tumor presented itself in early January 2024. Pathology identified it. Brain surgery in January, and radiation in February did their jobs.
The reproductive cancer was likely nipped when I did chemo back in mid 2021 for my breast cancer return. It just didn’t/couldn’t get this little offshoot that went to the brain & slowly grew. Physical problems presented themselves - not bloodwork - & scans confirmed. Breast cancer now turned down, malarian percolating in the special Natera/Signatera DNA disease test & in PET, not physically nor other bloodwork. And yes I have since gone skiing & did a 10 mile hike today.
My docs want me to be a person with cancer that is a small “c” - I am living with it. My “chronic” condition. We don’t react when monthly numbers change. Time of day, bad draws, diet, moon phase, really anything - can impact. We look for trends. We look at scans. We look at me. And how I am living my life. And then we react. I help myself & give them the best patient I can be through tracking my numbers, eating well, exercising, working & spending quality time with my family & friends. Who knows what will come but new treatments & sites like this give me hope! Good luck!

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Keep on truckin’! Inspirational and thank you for sharing.

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@windyshores

My oncologist doesn't do these blood markers at all. I am 9 years out and stopped letrozole at 5 years. I have no idea how I will know I am stage 4. How many of you have docs who do this testing?

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I am submitting blood every 6 mos. To Signatera. Due in August. I’ve had 3 negative results . Oncology will still say they don’t know what to do with a positive result.

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@sharon35981 and @anjalima I asked my oncologist some months ago about Signatera and they said no, they only prescribe if for those with metastasis, to keep track of treatment. Do either of you pay out of pocket and does the company let you order it yourselves?

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I have Medicare—Stage1–at lumpectomy. I get a Signatera test every three months. My oncologist orders this blood test to be taken every three months at my home. I pay $0.00.

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@keepmoving2

@tessspike. Good for you for being on top of your numbers. I am a big advocate on this site for tracking all your numbers on a chart for two reasons: 1) it helps a patient to know what is going on with their body & 2) to see trends. In your case, absolutely the knee replacement surgery can impact numbers. It might be helpful to track all your numbers a bit further back to day one. Maybe talk to your doctors to get a sense of when you can expect the surgery impact to lessen or request /look at your other numbers to see if the inflammation/surgery is reflected elsewhere. Docs like to see trends and like you pointed out, backup with scans, how you are feeling, etc. Fingers crossed for you. I am going on my 4th year as a MBC patient and have rebounded really well from when my initial meds stopped working 18 mos in. 2nd meds didn’t work but this third round seems to be doing the trick!

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Thank you for posting this. I have metastatic breast cancer and had a total left shoulder replacement eight weeks ago. I had noticed that my CA 27.29 has been rising. I just completed my bone scans chest and abdomen CT and they were all negative. I had to stop the
Ribociclib for 2 months . Three weeks prior to surgery and then another four weeks during my postop recovery. I restarted my ribociclib cycle three weeks ago and now my ANC has been .8 for the last two weeks.

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@sam2020

Hi, I'm new here. in Nov 2020, my wife was diagnosed with stage IV breast cancer-(hormone receptive) it has metastasized throughout her spine, and is in most of her bones. She takes Verzenio daily, gets scans every 3 months, sees oncologist and gets Zometa, and Faslodex every 4 weeks-(on this last visit we got him to change the Zometa to every 3 months, after we researched it and thought maybe it is causing some of her pain). Upon diagnosis she was in really bad shape, after months of treatment she improved, but recently her pain has been getting worse-(she wears a patch, and has some oral pain meds), her most recent CT showed no growth. That's the short of it, our concern is with her CA 27-29, her oncologist tells us not to pay too much attention to it. Upon diagnosis it was 676, it went down with treatment, and stayed between 90-105, 6 months ago it was 121, and has continued to go up, last week it was 213. Her Oncologist is an optimist, and won't give any prognosis, maybe we shouldn't worry, but with the severe pain, fatigue, high CA, we're wondering if the CT scans are missing something.. Does anyone else have or has had CA numbers this high?

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My CA 27-29 has been rising for 1 year now..went from 37 to 2880 now..have had many PET/CT, Bone scans, mannogram, ultra sounds, etc..PET/CT lit up under right arm this time..lymph node..went for a mammo and ultra sound with bioposy scheduled pending finding..and nothing could be found on mammo or ultra sound..we are all scratching out heads again..anybody have any clues???

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@oldandtired

My CA 27-29 has been rising for 1 year now..went from 37 to 2880 now..have had many PET/CT, Bone scans, mannogram, ultra sounds, etc..PET/CT lit up under right arm this time..lymph node..went for a mammo and ultra sound with bioposy scheduled pending finding..and nothing could be found on mammo or ultra sound..we are all scratching out heads again..anybody have any clues???

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@oldandtired, have you already had breast cancer and treatment, and CA 27-29 is monitored to check for recurrence or spread?

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@oldandtired

My CA 27-29 has been rising for 1 year now..went from 37 to 2880 now..have had many PET/CT, Bone scans, mannogram, ultra sounds, etc..PET/CT lit up under right arm this time..lymph node..went for a mammo and ultra sound with bioposy scheduled pending finding..and nothing could be found on mammo or ultra sound..we are all scratching out heads again..anybody have any clues???

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How'bout an MRI - still the gold standard? xoxo

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