The promise of hu3F8 is that it can be applied at significantly higher dosages than ch14:18 and 3f8 (2.5x) and is given to children as out-patients with significantly less side effects.
If anyone has any more information please post here.
My understanding is that the drug may be made available in Hong Kong and the UK soon as well.
We were at MSK for a vaccine injection today and our RN said there were a couple of nurses from London here this week to train in 3F8 administration. So looks like Madrid isn’t the only European city to be getting access to it…
london nurses probably came from harley street clinic where doctor Stergios Zacharoulis sent them to train . he brought 3f8 to this clinic as i was told by himself. but its 3f8 and not 3huf8 i think. MArk since you do the vaccine in MSK do you have any information about the stats? we hear that 3 years it has like 80% of remaining in remission. is this accurate?
Presentations by Brian Kushner and Shakeel Modak at various patient/parent nb conferences.
I did push Brian Kushner for more information but unsurprisingly he wasn’t very forthcoming!
I think the bottom line is no one really knows if it makes a difference and if so, how much of a difference. There are so many other variables at play in the small number of patients that we are talking about, so you have to be very careful how this limited data is interpreted.
For me, the vaccine:
makes sense biologically
seems to have limited significant side effects
the very limited data presented at conferences suggests there might be an improvement in survival (in patients who have previously relapsed) - but as I say there are so many confounding factors and the trials so far haven’t been set up to answer this question - the only published data I’m aware of is linked above and was a phase 1 trial that primarily investigated the maximum tolerated dose
and is something we could personally afford (after a lot of fundraising!)
… so for us it made sense to give it a shot!
Thanks for the response Mark. Of course for a relapse case seems logic to follow the vaccine. As fas as i know in memorial they started doing it also in all first remission patients . that is to be honest the thing that keeps going into my mind. If its a logic step to put a child in remission in this therapy.
Yes Sam – the goal is EMA and FDA approval. Trial should be open next month! I had the great pleasure of finally meeting Dr Mora from Barcelona (after years of email) at the AACR pediatric meeting in Dec – he is fantastic! Someone should make a movie out of this whole story some day.
The trial is open for relapse/refractory (bone and or marrow) but no trial for 1st remission. Best thing is to contact Dr Mora about 1st remission (frontline).
I met Dr Mora at a pediatric oncology meeting in the US last Dec, and haven’t been to Barcelona. I can put you in touch with families who have been there if you would like. What is the status of your child?
hi donna
thanks for your answer.
our little finished induction therapy incl. TVD and the coming wednesday she’ll have surgery, HDT is planned for early november.
would be great if you could connect me.
br jindrich
hi donna,
I hope you are fine, can you get back to me please.
we are back from HDT now and we would like to contact parents who went to spain.
thank you
jindrich