Weaning Myself off Nivo
After having been on combination immunotherapy (Ipi/Nivo) for three years, and having been NED at the last six of my regular three-monthly scans, I have decided to stop the treatment. The medical team thinks it has done all it can for me, and my immune system should be able to do the job by itself from now on (if needed). Furthermore, people going onto this therapy at present are only being given two years of it.
So in one way I feel as though I am throwing away my security blanket, but on the other hand that I am taking another step forward in my fight with cancer. I will continue to be monitored every three months as part of the trial protocol, but will no longer have to present at the chemo lounge every two weeks.
I still find it a bit surreal to think I have actually gotten away with having mRCC, which in the past was usually a very sombre prognosis. I am absolutely grateful to all the scientists who made this possible, together with all the various politicians, bureaucrats, drug companies, funding organisations and private donors who had the courage and vision to support scientific and medical research. And the nurses, doctors and clinical staff who daily continue to be at the forefront of the still daunting battle for people’s lives.
There is still a long way to go before we totally defeat cancer, and my own story may still have some further stages to it that I can only guess at, with no certainty of being permanently cured. However I feel that I represent a real achievement by the medical community, and sincerely hope that more and more others will come to benefit from this progress as I have.
And it is somewhat ironic and very sad to be posting this after just learning of Abunai’s passing. A bitter sweet moment.
Comments
-
Congrats & Thank you!
Congrats on reaching this milestone - WOW!! What a great success story. I wish you continued success. I also wanted to thank you - your participation and contributions during the clinical trial phase helped to make this powerful and live saving combination a first line treatment for those newly diagnosed with mRCC. My battle is still in the beginning stages but I am hopeful that one day I too can be NED because of IPI/NIVO. Good luck to you!
0 -
Quite a journey
You've been on quite a journey now it's on to the next step. My oncologist told me a couple of weeks ago he was taking a responder off nivolumab after 3 years. All the best to you and let's hope your cohort are trailblazers for lots of others coming after you.
0 -
if I had a drum
what a dude...
I love it when people do this... you are truly amazing
thank you for all you do
0 -
Fred
Fred
I am so thankful for you, you are definitely a trail Blazer I'm currently undergoing this treatment and so far it is working for me. You have offered your experience and advice concerning side effects. It's made life easier for me knowing you've been there. I'm so happy your results have been amazing.
0 -
Congratulations, your words
Congratulations, your words lift my spirit time. Thank you
0 -
Congratulations Fred!!! Keep
Congratulations Fred!!! Keep on keeping on!
0 -
Congratulations
Great to hear. Sending back some positive thoughts for you and your loved ones.
0 -
And again.
Hi, me back again. Another 3-monthly CT scan this week, and again no signs of disease. Bloods all good too.
I still can't believe my luck to have had this degree of success so far, and part of me is half expecting all of this to turn negative, but meanwhile I will continue to reap the benfit of the hard work by all the scientist, clinicians and volunteers who have gotten the immuno-therapy story to where it is today.
Best Wishes to all of you.
Fred
0 -
I read your profile and I
I read your profile and I think you have done very well. You have such a great attitude, and I admire your bravery. Sweet of you to mention all the people whom you appreciate along your treatment journey. For my husband, who was diagnosed stage 4 in 2012, it came as a surprise to us that we were the ones that had to decide on what treatment path to take. We had expected to be told what to do next. It's hard to make these decisions as lay people. My husband has been on Inlyta since 2013. All of his scans are negative since. He has chosen to continue taking the pills. It's certainly easier than an infusion. I think we are kindof afraid to stop. Because of it being a fairly new medication in 2012 there is no data for long term use. Docs dont really know what to tell us, as always. It's our choice.
I wish you the very best, and congratulations!
0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.9K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 398 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 671 Leukemia
- 794 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 237 Multiple Myeloma
- 7.1K Ovarian Cancer
- 63 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 540 Sarcoma
- 734 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.8K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards