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Wednesday, November 05, 2025 10:22:55 AM
Why do you think that patients in the placebo-arm who relapsed in the trial and then received DCVax-L much later than those in the active-arm group, did better?
Doc, I think we should also consider that these rGBM patients may have also “lived longer” because their returning tumors may have come back with a mesenchymal signature… which TMZ is known to induce in returning gliomas. And while mesenchymal GBM is pretty much the worst of the GBM subtypes (which may be why so many rGBM patients are so short-lived), DCVax-L works best on this subtype. A mesenchymal tumor is more of a “hot” tumor, so they can thereby better attract an immune response, should the TCells actually show up (which DCVax has proven it can effect).
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