Stage 4 Malignant Melanoma internal
I Stage 4 malignant melanoma in my small bowel and my liver. Both were surgically removed. I was on Leukine shots for almost 2 years. Just want to see if there are other people out there that experienced any of this diagnosis? Pam
Interested in more discussions like this? Go to the Cancer Support Group.
Hi I was diagnosed stage 4 metastatic melanoma on my liver September 2015. No primary cancer point. The tumor was 15cm X 8 cm.... Inoperable. Fortunately the immunotherapy is working . I asked my oncologist is I would ever get to the NED status and she was I don't think so. I'm stable , no spreading , and the tumor has shrunk a great deal.
Is there anyone that is in a similar situation?
Hi Meg, welcome to Connect.
You'll notice that I moved your message to this existing discussion about metastatic melanoma. Reading back through the earlier posts, it appears that Pam (@0716) has a similar experience of being diagnosed with metastatic melanoma found on her liver and small bowel.
In this group you'll also meet @twinskl @lynnkay1956 and @texas7777.
Meg, great to hear that the immunotherapy is working and there's no spread visible. We look forward to getting to know more about you.
Thank you. I am treated at Smilow Cancer Hospital which is part of theYale-New Haven Hospital in New Haven CT.
I did the 4 doses of the combo ( Yervoy & Opivido) I developed some sarcoids in my lungs and on my elbow, wrist, and knuckles. I had to stop opvido for 10 weeks and was treated with steroids by the pulmonologist.
Lungs are clear!
I have been on opvido since April 22,2016 every 2 weeks until Beginning of February and the protocol is now every 3 weeks.
I have fatigue and achy joints . I can live with that.
They do not know the primary area but do know the melanoma traveled thru my blood.
I had my last scans in January and there was no shrinkage from my previous scan 3 months prior. I have the MRI on my brain and a CT scan on chest, abdominal and pelvic areas.
So , I'm living with this and hope and pray that it will shrink and not spread!
Good news Meg4434 is that you are stable. Sounds like the combo of Yervoy/Opdivo did its work and reduced the tumor. It is my understanding that sometimes those drugs take time to work, so patience is impt. I pray your tumor continues to reduce.
I had been treated with Yervoy first, followed by Opdivo for my leg melanomas. I was lucky, after 2 infusions with Opdivo, all the melanomas disappeared - a true miracle. I could only withstand 6 infusions as my body went into total inflammation and Dr decided to stop the treatment. I still have some side effects (arthritis, joint pain, eye irritation, low sodium/hemoglobin counts) but all manageable. Prednisone has been my friend of late! But I am cancer free almost 2 yrs now, and very grateful.
Wish I could be of more help, but my experience has been limited, as the melanomas have not travelled beyond my leg, as of yet. I stay positive, but I do understand the melanomas are never curable, we just have to stay one step ahead.
Please simeoneone with liver melananoma write me.
Am having a y90 on Tues. I am so scared. This is all new to me. Please respond.
Do not be afraid Y90 is ok I got it feels I felt just little burning by my liver stomach since my cancer is liver mild pain because of the procedure my was by my leg going to my liver after that didn’t feel nauseous or chills just tiredness but again every body is diferente just be positive strong we got this F$&@ Cancer praying for you 🙏🏻🙏🏻
Thank you so much
After having a third Melanoma 8 years ago the first was negative and most recently 2 were positive 1 removed 5 years ago and 1 more 6 months ago, this last time 2 Lymph Nodes that were negative we have decided that the best move forward would be to start Keytruda. I have just had my first Keytruda infusion and feel great. No obvious side effects at this point, no loss of energy or pain!
Just checking in @mikenjoy76. How are you doing on Keytruda? How often do you get infusions?