Anyone on Opdivo (nivolumab) for metastic lung cancer?
I will be starting opdiva for treatment of lung cancer that has mestisised to lymphs. Does anyone have any feelings/opionins on it?
Interested in more discussions like this? Go to the Lung Cancer Support Group.
Yes, the Dr said that is possible if necessary. Might have to be on a lower dose, will have to see how my body reacts. I also asked if Keytruda would be a possibility in the future, but Dr said it is the same drug as Nivo so would make no difference. Dr's also mentioned a repeat of the isolated limb infusion, as well as IL2. Hopefully, will not have to go there...
I wish I could remember ! It was one of those times that you are searching for one thing (droplet metastisis) and then are lead on a path to many interesting things. I do believe it was a medical Journal but not sure which one. I know this is a drug that has great promise.
I have been diagnosed with both Thymic Carcinoma and Thymoma so I have spent hundreds of hours trying to find detailed information on these TWO cancers, as recently as 10 yrs ago some Dr.s considered them one and the same and/or Thymoma was not even listed as a cancer. Many times it happens that the more information I get the more confusing it becomes. So am hoping to find some people with Thymic Carcinoma , even my dr.s at Mayo-Rochester do not know why I am still alive my last onc. called me his miracle patient and I have truly been blessed.
Mayo clinic in Rochester Mn. has a Hope House for cancer patients and families I believe. Maybe someone here has info on how to contact them?
Yes, Hope Lodge provides housing for Mayo Clinic patients and families visiting Rochester for cancer treatment. Here is more information about the Sandra J. Schulze American Cancer Society Hope Lodge in Rochester, MN http://bit.ly/2jcqvR7
There is Gabriel House in Jacksonville: http://www.gabrielhouseofcare.org/ We stayed there when my husband had a kidney transplant in 2012. At that time it was $35/night.
My boyfriend begins a nivo-ipi trial tomorrow after first line chemo/radiation did not work. Originally diagnosed with Stage 3 NSCLC, shortly after ending first line treatment, bone pain led to a PET which showed metastatic NCSLC. It was likely Stage 4 all along, but was to micro to detect. He is really struggling with breathing, energy, appetite, etc. How long before we know if this treatment is showing positive results?