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Re: None

Tuesday, 05/17/2022 6:57:37 AM

Tuesday, May 17, 2022 6:57:37 AM

Post# of 704055
hoffmann6383

Member Level
Monday, May 16, 2022 4:34:46 PM

Re: None

Post#
474311
of 474525
Some great lines from Dr. Musella in his 5-15-22 presentation. He is the President of the Musella Foundation for Brain Tumor Information and Research, Inc. If you don't have time to listen to the entire presentation check out these points:

(some paraphrasing)


Quote:
The recent dcvax-l trial made excellent use of a synthetic control group and was the first major brain tumor trial to do it the right way!



Quote:
Dcvax trial was actually 20 years long. This is for people who live about a year or two, so you are talking about at least 10 generations of patients died waiting to find out if it is good when we kind of knew it was in the beginning and had very little side effects. So if we could have given it back then we could have saved 20 or 30,000 lives.



Quote:
lol, PFS is actually a good finding, but they probably shouldn’t have included this in the slide because it created so much confusion
Quote:
important thing is when they get to OS

Quote:
it is a valid control group

Quote:
Need to get fda approval now so we can start to use it and start combination trials on it

Quote:
We already know using an immune enhancer will make the vaccine work better, using a checkpoint inhibitor will make it work better, probably using optune will make it work better, so many combinations we can try
Quote:
Side effects is like getting the flu shot

pgsd

Member Level
Monday, May 16, 2022 11:48:00 PM

Re: None

Post#
474470
of 474527
Gregory Zivic, MD
@metacollectiveG
$NWBO by the way, DCVax-L trial had only 7 out of 331 patients with IDH-1 mutation (a now known beneficial mutation for survival) In the Optune trial $NVCR had almost 50% IDH-1 mutation. Let’s think hard about these issues please and keep focused. We have approvable data here.






Gregory Zivic, MD
@metacollectiveG

$NWBO Marnix Bosch at 32:32 of the presentation confirms only 7 out of 331 patients in #DCVax P3 trial were IDH-1 mutations. Thus IDH-1 status, which is a large part of most cohorts, did not contribute to the success of the P3 trial. And it WAS successful


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