The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

Any success taking Ippi and Nivo the 2nd time?

Forums General Melanoma Community Any success taking Ippi and Nivo the 2nd time?

  • Post
    Alydar77
    Participant
      I had a recurrence in my right lung in February and had my right lower lobe removed on 3-29-23. I had a pet scan on 6-6-23. It showed up a couple enlarged lymph nodes around my lung and a tumor on my adrenal glands.
      My last dose of Nivo was 3-14-17. I took it for 17 months and started out with 4 doses of ippi with nivo. I had a great response.
      My Dr at Vanderbilt wants to start me back on ippi and nivo.
      Has anybody had success taking the ippi and nivo the 2nd time? I’m very concerned that it will not work the 2nd time.
      Thanks,
      Alydar
    Viewing 2 reply threads
    • Replies
        Bubbles
        Participant
          Sorry you are dealing with this, Alydar. I have been lucky and not needed re-treatment. However, I have covered a lot of reports and data about using immunotherapy upon progression after having been treated with immunotherapy. Here is a link that covers that issue with many additional links within: immunotherapy after progression

          Bottom line from the research – yes, responses are highest in folks who have not had prior immunotherapy. HOWEVER, many who progress after being treated with immunotherapy – like the Yervoy/Opdivo combo – can attain good responses on a repeated regimen!!!

          Hope this helps. There are many other articles on the topic on my blog. Just use the search bubble if you are interested. I wish you my best. Celeste

          JudiAU
          Participant
            Thanks for the link Bubbles. I’ve always worried about this.
              Lucas
              Participant
                Bubbles data does not actually reflect a 2nd course of ipi/nivo. It reflects the data of using ipi/ nivo after failing pd1 as a mono therapy. The response rate of a 2nd course of ipi/nivo is about 25%. I’m in the same situation after recurring 4 years later after a complete response to ipi/nivo. I’m hoping to only be surgically respected, but am waiting on a pet scan after having a Ct. recurrence is rare after having a CR or PR. only about 10% of immunotherapy responders end up in this category. 11 0f 44 people responded again to ipi/nivo , but many more had responses when combined with radiation and/or surgery. I hope we both can find responses from treatment again.
              Bubbles
              Participant
                Hi Lucas,

                Perhaps you will find this more particular – was hoping the links within the post would be easy to follow – but here you go:
                Ipilimumab or ipi/nivo combo after recurrence in patients previously treated with immunotherapy ~

                Specifically, the second article reviewed in the post. There are many reports that indicate using the ipi/nivo combo rather than a single agent after progression on immunotherapy has better response rates. I think choosing what to do upon progression post immunotherapy has everything to do with how the patient experienced side effects to previous immunotherapy, their ability to tolerate or risk more side effects, BRAF status, disease status, personality, MD tolerance for all of the above, etc.

                Perhaps you will find this (and links within) pertinent to your hopes regarding a surgical treatment: Surgery After Systemic Treatment for Melanoma

                I wish you my best. Celeste

            Viewing 2 reply threads
            • You must be logged in to reply to this topic.
            About the MRF Patient Forum

            The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

            The information on the forum is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.

            Popular Topics