What may be the miracle drug we have all been waiting for might finally be here, in our lifetime. Denosumab, made by the drug company Amgen has been in clinical trail for awhile now and is showing a great response rate. You may have recently read Quintons latest blog where he is now in this clinical trial.
Back in April when I first discovered the trial in a media post, the trial was not open to pulmonary disease. After a rather simple effort to get the drug manufacture to open this trial to pe…
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Posted on December 15, 2008 at 10:04am —
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Did you have a biopsy in the last year before starting Denosumab? Right now that is my major hurdle with my insurance.
The research nurse in Pennsylvania also told me that Univ. of Fl. has been asked to participate. I have been in communication with them as well but they have not made their final decision. If they were a trial site though I would be only a 2.5 hour drive away. So right now I am trying to get into the trial but running into some obstacles with insurance so I would love to hear if they made you have a biopsy again and if so what type did you have.
Take care and good luck with the trial. I really have positive feelings that you are going to see a favorable response on your next scans.
I just wanted to check in and see how the Denosumab is going for you. Hope you start to feel better soon.
I am a little discouraged today because I am back on daily CBC's again. My platelets have been dropping lately and seem stuck in the 40's this week. Did you have this problem when you were on Interferon and how often did you have bloodwork done while on therapy? The manufacturer of PegIntron says technically the drug is supposed to be permanently discontinued if platelets fall below 50 but so far we just hold doses and do daily CBC's.
I hope your second injection was uneventful this week and everything is going well with you. Oh I also saw what you wrote about not having pictures on our profiles. I don't think anyone is worried about predators but in my case and maybe for others I know I hate to have my picture taken. I avoid a camera whenever possible but I'll try to get a picture up sometime if I can find a decent picture.
I have a question. Do you have to pay for the Denosumab? I am assuming since it is a clinical trial that the medication is free. I have really been thinking a lot about the trial. I looked at the requirements for it and you can not currently be undergoing any other treatment but I do not know how long you have to be off other treatment. I have 8 more months of PegIntron to go if I stay with it. I have an appt. with my local oncologist tomorrow and I am going to ask his opinion about switching. I kind of worry what if Denosumab is not effective for as many other conditions as they hoped but is for GCT. Then it may not be profitable for them to make it for such a small group. I've read mixed results about its effectiveness in other conditions.
Did your insurance cover your PegIntron and did you go somewhere for the shots or self administer? Sorry I keep asking you so much but our cases seem to be the most similar. It is also kind of unusual for us to have the metastases since neither of us ever had a recurrence. Some luck, huh? I am just grateful that mine has been as slow growing as it has been though MDACC just sent me my Chest CT report and according to the radiologist it grew more than what Dr. Ludwig thought. Usually they have the radiologist report when I am there but for some reason last time it had not yet been read so they were just looking and comparing themselves. Thanks for any info you can give me. I will really be paying attention to your case and I truly wish you the best of luck with this trial.
Mary
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