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.

Update – CT Scan results

Forums General Melanoma Community Update – CT Scan results

  • Post
    emilypen
    Participant

      Hi All,

      Just wanted to let you all know the good news! After 7 weeks on the trial drugs ( Mek & P13k) my husbands  scan results show "stable" disease. The measurements show that the tumours and bone lesions have experienced absolutely no growth!

      We were hoping for a reduction in size but as he feels so great and and its only been 7 weeks we're happy. Hopefully in the next scans in 2 months will show a reduction.

      Would love to hear how others on the Mek inhibitor have faired with their scans? was reduction immeadiate or did it take time?

      Hi All,

      Just wanted to let you all know the good news! After 7 weeks on the trial drugs ( Mek & P13k) my husbands  scan results show "stable" disease. The measurements show that the tumours and bone lesions have experienced absolutely no growth!

      We were hoping for a reduction in size but as he feels so great and and its only been 7 weeks we're happy. Hopefully in the next scans in 2 months will show a reduction.

      Would love to hear how others on the Mek inhibitor have faired with their scans? was reduction immeadiate or did it take time?

       

      thanks,

       

      Emily

    Viewing 3 reply threads
    • Replies
        lhaley
        Participant

          Great news!  Stable is good when someone has been having progression!  Take a deep breathe and enjoy the time between now and next scans.  Scan anxiety is hell!

          Linda

          lhaley
          Participant

            Great news!  Stable is good when someone has been having progression!  Take a deep breathe and enjoy the time between now and next scans.  Scan anxiety is hell!

            Linda

            killmel
            Participant

              Hi Emily,

               

              Happy to hear that the tumors are stable. How have the side effects been on GSKMEK for your husband??? What is P13K??? Do you know the clinical trial number …NCT

              Hope you get shrinkage next scans

                emilypen
                Participant

                  The side effects have been minimal so far. Some rash on his face and back, slightly more sensitive stomach and a little fatigue. The clinical trial # is http://clinicaltrials.gov/ct2/show/NCT01155453.

                  Given the disease was progressing incredibly quickly in the 2 months previous to him starting the trial, we're thrilled.

                  Emily

                  emilypen
                  Participant

                    The side effects have been minimal so far. Some rash on his face and back, slightly more sensitive stomach and a little fatigue. The clinical trial # is http://clinicaltrials.gov/ct2/show/NCT01155453.

                    Given the disease was progressing incredibly quickly in the 2 months previous to him starting the trial, we're thrilled.

                    Emily

                  killmel
                  Participant

                    Hi Emily,

                     

                    Happy to hear that the tumors are stable. How have the side effects been on GSKMEK for your husband??? What is P13K??? Do you know the clinical trial number …NCT

                    Hope you get shrinkage next scans

                Viewing 3 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