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.

Phase II Study of Glembatumumab Vedotin… any insights or experiences?

Forums General Melanoma Community Phase II Study of Glembatumumab Vedotin… any insights or experiences?

  • Post
    BeckSTAR
    Participant

    Hello, I am new to this site.  My father was diagnosed with stage IV melanoma, summer of 2015.  (inital spots removed from skin on and off years ago, big one was from neck that they think must have spread even with removal of lymph with clear biopsy… despite routine check ups the metastasis was caught very late).  Summer 2015 showed a large tumor in liver and small spots in lung and gluteal areas.  He did well on Pembro, lasted almost 1.5years (until a couple weeks ago) without any resistance.  All spots disappeared except a "shell" of the liver tumor, which is now growing again.

    Now he is about to start Glembatumumab Vedotin next week after all the biopsy/scans/testings are completed for the study.  Anyone currently on this study or have experience with it?  Things to expect, look out for?  I am a nurse myself, but all this is pretty new to me.  I take care of the little humans (peds). 

    My father is 67, but in shape/active… walks/jogs every morning and head captain/manager of a small marina. 

    Thanks in advance,

    A concerned daughter heart

Viewing 11 reply threads
  • Replies
      Patina
      Participant

      Can they do stereotactic body radiation therapy with keytruda or another immunotherapy followed shortly after? – Hoping for an abscopal effect.

        BeckSTAR
        Participant

        I haven't heard any talk about radiation at this point.  They may include another medicine/immuno with the Glem Ved but I am unsure what that is or how that is decided.  Since it is all a clinical trial I think he has to follow the constants that they need to keep.  So right now it is Glem Ved on it's own or Glem Ved + another med.

        BeckSTAR
        Participant

        I haven't heard any talk about radiation at this point.  They may include another medicine/immuno with the Glem Ved but I am unsure what that is or how that is decided.  Since it is all a clinical trial I think he has to follow the constants that they need to keep.  So right now it is Glem Ved on it's own or Glem Ved + another med.

        BeckSTAR
        Participant

        other med it may be in combination with is varlilumab.

        He is BRAF negative from what I read up on his biopsy from last year.

        BeckSTAR
        Participant

        other med it may be in combination with is varlilumab.

        He is BRAF negative from what I read up on his biopsy from last year.

        BeckSTAR
        Participant

        other med it may be in combination with is varlilumab.

        He is BRAF negative from what I read up on his biopsy from last year.

        BeckSTAR
        Participant

        I haven't heard any talk about radiation at this point.  They may include another medicine/immuno with the Glem Ved but I am unsure what that is or how that is decided.  Since it is all a clinical trial I think he has to follow the constants that they need to keep.  So right now it is Glem Ved on it's own or Glem Ved + another med.

      Patina
      Participant

      Can they do stereotactic body radiation therapy with keytruda or another immunotherapy followed shortly after? – Hoping for an abscopal effect.

      Patina
      Participant

      Can they do stereotactic body radiation therapy with keytruda or another immunotherapy followed shortly after? – Hoping for an abscopal effect.

      Jeanne321
      Participant

      Hi – I have been on this trial for a year and a half. Each scan has shown shrinkage and side effects, after decreasing the initial strength, are very tolerable. I'm in the same age range as your Dad. Good luck to him. 

      Jeanne321
      Participant

      Hi – I have been on this trial for a year and a half. Each scan has shown shrinkage and side effects, after decreasing the initial strength, are very tolerable. I'm in the same age range as your Dad. Good luck to him. 

        BeckSTAR
        Participant

        Wow, that is amazing!  Thank you for this reassurance, I am hoping that this works awhile for him also.  After reading a bit on the trial it mentioned that having a rash initially may be indicative of it working better/longer? Did you experience any rash?  We did receive some good news today that looks like they will start it on Monday, a few days earlier…fingers crossed!  Good luck to you also.

        BeckSTAR
        Participant

        Wow, that is amazing!  Thank you for this reassurance, I am hoping that this works awhile for him also.  After reading a bit on the trial it mentioned that having a rash initially may be indicative of it working better/longer? Did you experience any rash?  We did receive some good news today that looks like they will start it on Monday, a few days earlier…fingers crossed!  Good luck to you also.

        Jeanne321
        Participant

        Yes, rash was severe initially which was one reason that the dose was lowered. Since then I get the rash on day 3 after infusion, it only lasts about 5 days and is managed with Sarna lotion or steroid cream. 

        Jeanne321
        Participant

        Yes, rash was severe initially which was one reason that the dose was lowered. Since then I get the rash on day 3 after infusion, it only lasts about 5 days and is managed with Sarna lotion or steroid cream. 

        Jeanne321
        Participant

        Yes, rash was severe initially which was one reason that the dose was lowered. Since then I get the rash on day 3 after infusion, it only lasts about 5 days and is managed with Sarna lotion or steroid cream. 

        BeckSTAR
        Participant

        Wow, that is amazing!  Thank you for this reassurance, I am hoping that this works awhile for him also.  After reading a bit on the trial it mentioned that having a rash initially may be indicative of it working better/longer? Did you experience any rash?  We did receive some good news today that looks like they will start it on Monday, a few days earlier…fingers crossed!  Good luck to you also.

      Jeanne321
      Participant

      Hi – I have been on this trial for a year and a half. Each scan has shown shrinkage and side effects, after decreasing the initial strength, are very tolerable. I'm in the same age range as your Dad. Good luck to him. 

      ed williams
      Participant

      Hi Beckstar, where is your dad being treated? Also what did the oncologist say in regards to early results with the drug conjugate (glembatumumab)? Best wishes!!!Ed

      ed williams
      Participant

      Hi Beckstar, where is your dad being treated? Also what did the oncologist say in regards to early results with the drug conjugate (glembatumumab)? Best wishes!!!Ed

        BeckSTAR
        Participant

        Under Forida Cancer Specialists and Research Institute in Naples, FL.  My parents just vagely said "it's like Pembro"…should shrink/stop progression and his symptoms/pain should relieve within a couple weeks of starting hopefully. I am not there and haven't been able to speak to the MD.  It's frustrating because I am so far away (in Cali) although I'm taking FMLA to go be there for a month so hopefully can be more involved. 

        BeckSTAR
        Participant

        Under Forida Cancer Specialists and Research Institute in Naples, FL.  My parents just vagely said "it's like Pembro"…should shrink/stop progression and his symptoms/pain should relieve within a couple weeks of starting hopefully. I am not there and haven't been able to speak to the MD.  It's frustrating because I am so far away (in Cali) although I'm taking FMLA to go be there for a month so hopefully can be more involved. 

        BeckSTAR
        Participant

        Under Forida Cancer Specialists and Research Institute in Naples, FL.  My parents just vagely said "it's like Pembro"…should shrink/stop progression and his symptoms/pain should relieve within a couple weeks of starting hopefully. I am not there and haven't been able to speak to the MD.  It's frustrating because I am so far away (in Cali) although I'm taking FMLA to go be there for a month so hopefully can be more involved. 

      ed williams
      Participant

      Hi Beckstar, where is your dad being treated? Also what did the oncologist say in regards to early results with the drug conjugate (glembatumumab)? Best wishes!!!Ed

      Bubbles
      Participant

      Here is an older link to a blog post I created re some of the initial work done with these meds:  http://chaoticallypreciselifeloveandmelanoma.blogspot.com/2014/10/another-antibody-drug-conjugate-for.html

      I think progress has been made in some of the antibody-drug-conjugates.  But thought is might interest you to see some of the background.  I wish you and your dad well.  Celeste

       

      Bubbles
      Participant

      Here is an older link to a blog post I created re some of the initial work done with these meds:  http://chaoticallypreciselifeloveandmelanoma.blogspot.com/2014/10/another-antibody-drug-conjugate-for.html

      I think progress has been made in some of the antibody-drug-conjugates.  But thought is might interest you to see some of the background.  I wish you and your dad well.  Celeste

       

        ed williams
        Participant

        I was looking at some of the information on Glembatumumab from the home page of the drug company that makes it called Celldex. If you clink on the link then look under "Pipeline" or "Investors and Media- then choose Press Releases." you should find some pretty good explainations of the various trials and they even give data of earlier trials etc. It wasn't that long ago that I was listening to Dr. Omid Hamid of the Angeles Clinic talking about what was coming in the future and Drug Conjugates were one to the paths along with CD27 a stimulating pathway for t-cell production. The future has arrived, so happy that more and more options keep opening up. Best wishes!!!Ed http://www.celldex.com/index.html

        ed williams
        Participant

        I was looking at some of the information on Glembatumumab from the home page of the drug company that makes it called Celldex. If you clink on the link then look under "Pipeline" or "Investors and Media- then choose Press Releases." you should find some pretty good explainations of the various trials and they even give data of earlier trials etc. It wasn't that long ago that I was listening to Dr. Omid Hamid of the Angeles Clinic talking about what was coming in the future and Drug Conjugates were one to the paths along with CD27 a stimulating pathway for t-cell production. The future has arrived, so happy that more and more options keep opening up. Best wishes!!!Ed http://www.celldex.com/index.html

        BeckSTAR
        Participant

        I read up a little on the website but will def look into the media stuff.  Thanks!  I'm a little anxious right now becuase now he's in the ER for some infectious concerns…. I hope this doesn't delay the study med too much.  At least they ruled out a clot, now thinking cellulitis.  The nurse in me is concerned it is more tumor though :/ 

        BeckSTAR
        Participant

        I read up a little on the website but will def look into the media stuff.  Thanks!  I'm a little anxious right now becuase now he's in the ER for some infectious concerns…. I hope this doesn't delay the study med too much.  At least they ruled out a clot, now thinking cellulitis.  The nurse in me is concerned it is more tumor though :/ 

        BeckSTAR
        Participant

        I read up a little on the website but will def look into the media stuff.  Thanks!  I'm a little anxious right now becuase now he's in the ER for some infectious concerns…. I hope this doesn't delay the study med too much.  At least they ruled out a clot, now thinking cellulitis.  The nurse in me is concerned it is more tumor though :/ 

        ed williams
        Participant

        I was looking at some of the information on Glembatumumab from the home page of the drug company that makes it called Celldex. If you clink on the link then look under "Pipeline" or "Investors and Media- then choose Press Releases." you should find some pretty good explainations of the various trials and they even give data of earlier trials etc. It wasn't that long ago that I was listening to Dr. Omid Hamid of the Angeles Clinic talking about what was coming in the future and Drug Conjugates were one to the paths along with CD27 a stimulating pathway for t-cell production. The future has arrived, so happy that more and more options keep opening up. Best wishes!!!Ed http://www.celldex.com/index.html

        BeckSTAR
        Participant

        Great! Haven't seen this info so thanks so much for sharing.

        BeckSTAR
        Participant

        Great! Haven't seen this info so thanks so much for sharing.

        BeckSTAR
        Participant

        Great! Haven't seen this info so thanks so much for sharing.

      Bubbles
      Participant

      Here is an older link to a blog post I created re some of the initial work done with these meds:  http://chaoticallypreciselifeloveandmelanoma.blogspot.com/2014/10/another-antibody-drug-conjugate-for.html

      I think progress has been made in some of the antibody-drug-conjugates.  But thought is might interest you to see some of the background.  I wish you and your dad well.  Celeste

       

Viewing 11 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