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.

Hyper progression, how often does it happen?

Forums Cutaneous Melanoma Community Hyper progression, how often does it happen?

  • This topic is empty.
  • Post
    Daisy2018
    Participant
      Hello fellow melanoma fighters and families.
      What do we know about hyper progression on Keytruda, Optivo/Nivo?
      I had my first scan results last week after starting on Keytruda 3 months ago.
      I had no detectable tumors 3 months ago before starting Keytruda and now it looks like lots of areas of lymphadenopathy on the PET scan. Something on my sternum as well.  Nothing looks big but is does look suspicious. I read there is pseudo progression, progression, and hyper progression.
      I read that sometimes there is phenomen with check point blockage  agents in immunotherapy medications when immunotherapy makes it progress quickly  instead of shrinking. In this case it should stopped be fast.

      I m having biopsy in my lungs tomorrow to make sure if this green eyed monster sitting there or not.

      From what I read the prognosis is not good when people respond this way to treatment. . Little worried here. Any ideas, suggestions? I m actually terrified here.

      Should I plan a farewell party while I m still able to do anything fun? I m kind of serious here.
      I looked at Costa Rica rentals. Should I cash out my retirement account get my family there and party away for one last time?
      Thanks!

    • 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