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.

cannot decide if i should do 30 day ifrn for stage 2 mel

Forums General Melanoma Community cannot decide if i should do 30 day ifrn for stage 2 mel

  • Post
    bball
    Participant

      I have ruled out 1yr interferon treatment. However,when i look at some of the trials like Rusciani it seems worthwhile to at least try it for 30 days to extend chances of DFS.(or has this study been shown not to be valid). Any experiances or opinions would be greatly appreciated.

      I have ruled out 1yr interferon treatment. However,when i look at some of the trials like Rusciani it seems worthwhile to at least try it for 30 days to extend chances of DFS.(or has this study been shown not to be valid). Any experiances or opinions would be greatly appreciated.

    Viewing 1 reply thread
    • Replies
        triciad
        Participant

          I completed the year of interferon in October.  My doctor initially said for me to just do the one month of high dose.  I tried the low dose and did pretty well with it, so I kept going.  When I was close to finishing the year, he told me it was a good thing because that study  (month of high dose is just as effective) was shown not to be reliable.

          Having said that, you have to do what is best for you.  Any decision you make is the right decision…never look back.  I didn't know that they offered interferon to stage 2.

          Best of luck with whatever decision you make.  I know it's not an easy place to be, but know that you have a strong support group here.

          Tricia – Stage 3B

          NED 18 months

            bball
            Participant

              Tricia, thanks for your response. One onc told me the 30 day high dose was in testing stage and no results but if i could handle it ,it may help but you never would know ,only if it did not help. Sre you doing any special diet, i.e. no sugar, lots of veggies etc.?  After treatment are you just doing follow ups?

              Glad you are doing well . It helps to hear that.

              bball

              bball
              Participant

                Tricia, thanks for your response. One onc told me the 30 day high dose was in testing stage and no results but if i could handle it ,it may help but you never would know ,only if it did not help. Sre you doing any special diet, i.e. no sugar, lots of veggies etc.?  After treatment are you just doing follow ups?

                Glad you are doing well . It helps to hear that.

                bball

              triciad
              Participant

                I completed the year of interferon in October.  My doctor initially said for me to just do the one month of high dose.  I tried the low dose and did pretty well with it, so I kept going.  When I was close to finishing the year, he told me it was a good thing because that study  (month of high dose is just as effective) was shown not to be reliable.

                Having said that, you have to do what is best for you.  Any decision you make is the right decision…never look back.  I didn't know that they offered interferon to stage 2.

                Best of luck with whatever decision you make.  I know it's not an easy place to be, but know that you have a strong support group here.

                Tricia – Stage 3B

                NED 18 months

            Viewing 1 reply thread
            • 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