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Colon cancer stage IV recurrence
It has been discovered that I have colon cancer again, which was not detected during my routine physical examinations.
In February 2024, cancer began to emerge, and was detected in November 2024.
My cancer has metastasized especially to my ribs with a 5 cm mass. The doctor has advised me that this is not cancer bone, but that it is the same type of cancer as mine, colon cancer stage IV.
My treatment has already consisted of five rounds of radiation and I am currently receiving Capecitabine.
A second opinion was obtained, which suggested that I should first undergo a biopsy, and based on the results, they could determine what treatment is appropriate.
Are there any comments?
Thanks.
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stage 4 with metastatis should be treated aggressively for a cure. A biopsy should absolutely be performed followed by surgery since it sounds the tumor is isolated and assessable. If this was not advised than a second opinion is definitely in order. Otherwise Stage 4 may have a survival of only 6 to 11 months. I know, tough news , but being involved is so important
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1 ReactionI will provide updates as I progress through the process. Thank You.
What kind of cancer is it? Do you have neuroendocrine tumors?
According to the doctor, this is a colon cancer that has metastasized to the lung, peritoneum, and chest wall. During a PET CT scan conducted on January 7, it was determined that.
They are scheduling the time for the biopsy; I will have an intercostal nerve block on February 20 and receive Folfiri infusions every two weeks; I may be transitioned to a maintenance treatment program of Capecitabine versus observation.
It is being considered whether they should use Xeliri instead of Folfiri due to my dissatisfaction with the pump and the use of Vectibix remains an option.
Hi Clau1117!
Sounds like we are on similar timelines. I am sorry it has progressed so far so fast in you. Mine also was not caught on scans and I was having them every 6 weeks to monitor but they didn’t go low enough in the pelvic region. I ended Folfox in February of 24 and started folfiri in December. I found that this time around carrying the ball and chain is no big deal when comparing it to the time it will buy me with my son. The hair loss is hitting me the hardest. You have to do what’s best for you. But I would go aggressive. They will be adding avastin (bevacizumab) to the folfiri which kills the blood supply to the cancer while the folfiri tries to kill it. No timeline for ending treatment this go round. I am buckled in for a long haul 🙂 I pray you have a huge loving support system at home and I will pray for you! God bless and stay strong! Was it right side or left side for you original crc? Mine was on the right…
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5 ReactionsMy husband had colorectal surgery in 2016. Early in 2022 he started having problems having a BM. His cancer was back, stage 4 spread to his lungs. He had chemo for a year with the pump. He lost all his hair, eyelashes, nose hair, etc. in July he started on Lonsurf. It has kept the tumors in his lungs under control except for one bigger tumor that keeps growing. He had a biopsy and it is the colorectal cancer so ee are waiting on results to see how to treat it. He has days where he sleeps about 20 hours and days where we go for walks. Just grateful for everyday
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2 ReactionsHay que tener fé, Dios es el que decide hasta cuando estamos en este mundo, espero que todo se solucione.
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1 ReactionHello !
The pain is on my left side, and it has been getting worse over the past few months; after my regular check-ups, I used to tell my husband, "At least I know this pain is not cancerous."
In 15 days, I will receive Vectivix, which looks a bit rough, but I will keep you posted.
My best wishes are with you as you embark on your journey, and I pray that you and your son have a very long life together.
Warm regards,
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1 ReactionGosh I googled it and had a bodily reaction to the word disfigurement! I hope its not a quasimoto effect! I will pray for minor effects! I just shaved my head last night and my son said it feels like a hairless cat! Lol He’s a character! He’s 17, on the spectrum. I want so many years with him! Its my only fear. I need to see him get thru college. I want to see him get his dream accomplished. Sigh. I will trust that God will get me thru it. My fingers and feet peel and I lose my fingerprints. That might happen to you. Diarrhea is not fun but they make pills for that. Yeast infections from steroids not fun, but they make pills for that too! If your treatment doesn’t work I would ask about the folfiri. I know you don’t want the chemo bag…. But after a while it just becomes a thing. It doesn’t define you. It’s hard to know that and to feel that. You’re strong. You can do anything you have to do. ❤️
I have stage IV . My oncologist prescribed ipi-novi immunotherapy infusion. 1st stage treatment protocol. Based on all the scientific data-this is the best protocol according to my oncologist team. I visited the Mayo Clinic and after spending a week there my oncologist there all agreed that I was receiving the standard of care and that they were in agreement with my local doctor’s protocol treatment. My tumor tissue was biopsy and sent to a 3rd. Party specialist who performed a genomic test checking for lynch disease and to verify if additional genetic boutique treatments are necessary to aid in my treatment plan. Not sure if this is helpful but I hope so.