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hope4patients

09/16/21 7:15 PM

#402525 RE: Lykiri #402522

Great post. Thanks

ATLnsider

09/16/21 7:26 PM

#402526 RE: Lykiri #402522

Lykiri, thank you for posting those transcribed remarks from Dr. Liau. It adds a lot of additional context.

Dr Bala

09/17/21 12:27 AM

#402559 RE: Lykiri #402522

Thanks, Lykiri, for the transcription of LL's reasonings regarding comparison with the ECAs in the case of GBM.

CherryTree1

09/17/21 7:42 AM

#402580 RE: Lykiri #402522

Great post Lykiri, thanks for sharing.

eagle8

09/17/21 8:02 AM

#402583 RE: Lykiri #402522

Thank you Lykiri and sentiment.

Best to you.

sentiment_stocks

09/17/21 10:01 AM

#402610 RE: Lykiri #402522

Just a quick thought… the DCVax-L trial was truly randomized. No one knew which patient was treatment or control. And since there were very likely treatment patients who appeared to event early (due to the pseudoprogression caused by DCVax-L), it was likely even harder to tell who was who as those patients you likely have thought (initially) were control patients! Anyhow, my bigger point is that this trial was a randomized controlled trial. And so, too, were the trials from which the ECA (external control arms) that will be used to compare the DCVax treatment arm to. So the trial purists out there could/should consider that both the treatment arm and the ECAs will have both actually been drawn from fully randomized control trials… just not for the same trial. I’d think, then, that there would be little to no discoverable bias, then, as the intent had always been (at least for the full term of the trial) to not treat the treatment arm of the DCVax trial as a single arm trial.