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.

mek/chemo reduction question

Forums General Melanoma Community mek/chemo reduction question

  • Post
    sharmon
    Participant

    Hi,  Brent has been stable on the Gsk mek/ chemo combination for 18 months.  14 of those months with mek alone. When he progressed then they added Alimta. So for the  last 4 months and with chemo added he has been stable again.  The problem is the chemo is very hard on him.  He almost always lands in the hospital after his infusion.

    Hi,  Brent has been stable on the Gsk mek/ chemo combination for 18 months.  14 of those months with mek alone. When he progressed then they added Alimta. So for the  last 4 months and with chemo added he has been stable again.  The problem is the chemo is very hard on him.  He almost always lands in the hospital after his infusion.   Two months ago they reduced the chemo and there was no difference.  This past week when he went in for the infusion his blood counts were too low.  So he has to go back in two weeks to see if he can receive the chemo at an additional 25% reduction.  What he has been on is working to keep him stable.

    Has anyone been through the reduction of chemo and does it get better at the lower doses?  We have another trial he can move to in October using two inhibitors. These two new inhibitors are not from GSK.  It is scary to move, but the chemo does reduce his quality of life.  And there is no way of knowing if the new combo will even work for him.

    If we choose to move to the new combo then we need to not do the upcoming infusion to begin the washout  period. 

    If anyone has any thoughts or has been through a similar experience I could use some input. 

    Thankyou for all your help and input.  This forum has kept me sane.

    Sharmon

Viewing 3 reply threads
  • Replies
      killmel
      Participant

      Hi Sharmon,

       

      I am so sorry to hear about the chem problems for Brent. If things werenot  bad enough.

      You mentione that you can move to another trial using two new inhibitors.

      Perhaps, you should post the new trial name,what are the 2  inhibitor, and/or NCT clinical trial number to see if anyone can give you feedback on that new trial. Maybe someone is on the new trial.

      Hope things get better for Brent.

      Dave

      killmel
      Participant

      Hi Sharmon,

       

      I am so sorry to hear about the chem problems for Brent. If things werenot  bad enough.

      You mentione that you can move to another trial using two new inhibitors.

      Perhaps, you should post the new trial name,what are the 2  inhibitor, and/or NCT clinical trial number to see if anyone can give you feedback on that new trial. Maybe someone is on the new trial.

      Hope things get better for Brent.

      Dave

      washoegal
      Participant

      It would also be helpful if you filled out a brief profile.  Is he BRAF positive?  What other things has he tried?  Is there any brain involvement?  We have some really smart people here and some folks who have been through it ALL.  So more info is good.

      Best of Luck

      Mary

      Stage 3

      washoegal
      Participant

      It would also be helpful if you filled out a brief profile.  Is he BRAF positive?  What other things has he tried?  Is there any brain involvement?  We have some really smart people here and some folks who have been through it ALL.  So more info is good.

      Best of Luck

      Mary

      Stage 3

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