Four-year survival rates for ipilimumab
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June 13, 2013 at 6:35 pm #21369
Steven
ParticipantAccording to this study ( http://www.ncbi.nlm.nih.gov/pubmed/23666915 ) 10mg has higher survival rates than 3mg. Does anyone know if studies are ongoing regarding best dosage?Does the FDA ever change a dosage once approved?
June 14, 2013 at 7:26 pm #61329Catherine Poole
KeymasterThere is more to come on this. It is only phase II results. Look to the combination trial, phase III just accruing. June 19, 2013 at 10:45 pm #61330Kpage
ParticipantHi there! My mother was just diagnosed with this cancer a couple months ago and I am looking for all the answers and best treatment possible. What can any of you tell me. She had her sinus surgery and they removed the cancer they could see and now starts radiation next week. She is in Pittsburgh PA…
Do you recommend taking her to another city?
She has some of the best docs around I here.
Just any advice, suggestions, opinions, anything to help my family understand and cope would be great!
June 20, 2013 at 1:18 am #61331Catherine Poole
KeymasterIs she at UPMC? They should have the latest treatments. Otherwise, a second opinion is always a good thing. Have you thought of Sloan Kettering in NY or possibly UPENN in Philly? Are they considering some type of systemic treatment? June 20, 2013 at 1:29 am #61332Kpage
ParticipantHi Catherine! Thanks for responding…
She is seeing docs from UPMC…
We found out the Tumor is grade 4 but the stage of cancer not sure yet. It has spread to fatty tissue but no organs.
We are doing immunotherapy after radiation…
This cancer is just mind boggling and so rare. We haven’t been given a prognosis… Is this normal?
Any therapy you suggest or heard that works better for sinus cancer …?
Thanks so much!
June 20, 2013 at 11:13 am #61333Catherine Poole
KeymasterAre they calling it Mucosal Melanoma? Then it would be Braf negative and immunotherapy such as Yervoy or PD1 would be best to try. Keep asking questions. What type of immunotherapy are they suggesting? June 21, 2013 at 2:57 am #61334flvermonter
ParticipantHi, I am new, and my husband is stageiiic melanoma and stage 1 non small cell lung cancer. We meet with the 2 different oncologists next week. Any thought or trials that I should be asking about that may treat both cancers? He is going to Moffitt Cancer Center in Tampa, FL. They removed all lymphnodes on the right side 10 days ago and he had alot of disease. He is BRAF negative. That is all i have to date. Thanks for any suggestions/experience/guidance. Regards, Mary
June 21, 2013 at 1:38 pm #61335Linny
ParticipantYou may want to see if he can qualify for a MAGE vaccine trial. Currently this vaccine is being tested for both melanoma and non-small cell lung cancer. The main catch is that the cancer cells have to test positive for MAGE. I know they’re doing a Phase III trial for it for melanoma because I’m in that trial. However, they no longer are accepting participants for it. Don’t know anything about the status of the lung cancer study, which is called MAGRIT. The melanoma study is called DERMA.
This is something you may want to ask your oncologist about. The folks at Moffitt should definitely know about these particular trials. This vaccine is being tested in other trials for melanoma and not just the one that I’m in.
June 21, 2013 at 9:36 pm #61336flvermonter
ParticipantThanks for the information for the MAGE trial. We meet with the lung Onc on Wed next week and the melanoma Onc the following week at Moffitt. Will bring my notes June 26, 2013 at 1:41 am #61337Linny
ParticipantDon’t click those links, that’s a spam message. June 27, 2013 at 4:55 pm #61338Catherine Poole
KeymasterThanks Linny, thought I had caught them all, please let me know when you see spam. I will delete and ban right away October 11, 2013 at 11:32 am #61339Ivelina
ParticipantKpage wrote:Hi there!
My mother was just diagnosed with this cancer a couple months ago and I am looking for all the answers and best treatment possible. What can any of you tell me. She had her sinus surgery and they removed the cancer they could see and now starts radiation next week. She is in Pittsburgh PA…
Do you recommend taking her to another city?
She has some of the best docs around I here.
Just any advice, suggestions, opinions, anything to help my family understand and cope would be great!
Hi, Kpage!I`ve been in the same situation, faced with the same diagnosis given to a member of my family.
The cases of mucosal melanoma are more rare and unfortunately more complicated as it concerns to taking decisions for the right therapy and the right way to go.
However, from experience with the case of my family member, I would say that you should rather try the immunotherapy such as Yervoy or PD1. As for the radiation, if well tolerated by the physique of your mother, could be a good therapy combination too.
However, each case is particular and you should also consult the docs.
Never give up and keep on fighting! I keep my fingers crossed for you and your mother!
Regards,
Ivelina
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