Jump to content

Trial, Progression, and next steps


Recommended Posts

Hi everyone,

My doctor stopped the trial since my CT scan showed at least 20% progression in all ten of the nodules which means the treatment was not working at all.

So, after 7 weeks, I now have a few options. Since my mutation is KRAS G12D which is currently being researched a lot, there is hope for a more targeted treatment in the future. 

But, for now, looks like a new trial will be activated in about 3 ish months and it will target all forms of RAS (including KRAS, and of course that means healthy RAS that is in our bodies). At this point, I don't know what the side effects could be, when it starts, the intensity of the schedule, etc.. 

I will check in with my doc in about a month and also try to schedule an appointment with the doc who is in charge of this new trial to see what information he could give me about it.

So, for now, I wait, and wait...while the "gradual growing nodules" continue what they are doing...

 

Best,


Ro

Link to post
Share on other sites

Ro,

Read Free and Invaluable on the Stay The Course blog. (I can’t link it because I’m using my phone). There is an email address in that blog for the National Institute of Health Lung Cancer research team. Write them and tell them of your DX and treatments thus far. They may have ideas. 

Stay the course. 

Tom

Link to post
Share on other sites

Oh Ro- that sucks! I wonder if the trial is working for anyone else.  Hopefully the investigators will learn why there wasn’t a response in the protocol, because of your willingness to participate this could be invaluable data. 

We’ll continue to pray that these are slow growing nodules with hope on the horizon for the next clinical trial. 

Back to the waiting game- Tom Petty got it right.   We’re all here for you! 

Michelle

Link to post
Share on other sites

Hi Everyone,

Thanks so much for all of your support. I'm used to the waiting part, but this is tougher given the fact that the cancer is actively progressing even if at a slower rate than some cancers.

I'll travel to NYC to hear more details about my next potential trial. In the meantime, it gives more and more research a chance to be happening directed to KRAS G12D.

Has anyone out there been on MEK inhibitors? I'm wondering about side effects because I know the new trial uses Mek inhibitors downstream going after RAS. However,  it would go after all RAS in the body, not just where the cancer is..so I'm interested to know what side effects there are in that situation.

 

Thanks again,

Best, 
Ro

Link to post
Share on other sites

Tom,

Thanks for the suggestion.

I'll check it out. FYI-The trial I was just on involved the use of the personal cancer vaccine + immunotherapy (Tecentriq)- but it didn't work.

Take care,

Ro

Link to post
Share on other sites

Tom,

I did email them. How does it work? Would I then need to go to Bethesda another medical opinion?

They asked me to send scans, etc..


Thanks,

Ro

Link to post
Share on other sites

Ro,

From what I understand, you'd be invited to Bethesda at the government's expense. They'd give you a complete diagnostic and determine if you would fit one of their ongoing studies. If not, they may tailor a unique study for you.  All examinations, diagnostics and treatments are at no expense to you, including travel and lodging and meals during treatment.  So that is a good thing and I do hope they can help you.

If you do decide to go to Bethesda, please consider reporting on your experience.  Many here would benefit from a first hand report.

Stay the course.

Tom

Link to post
Share on other sites

Hi Roz,

really sorry you have to change your care plan again, I admire your think forward attitude to the next thing, believing in a future helps us get to a future. When I got my swollen lymph node last Nov. you were there to help and I quote you "I'll keep sending you positive vibes!!   and now I will do the same and keep sending you positive vibes.  

I hope your able to get into the trial that Tom told you about.. please post as you find your new way.

Link to post
Share on other sites

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.

Guest
Reply to this topic...

×   Pasted as rich text.   Restore formatting

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

×
×
  • Create New...