I think the NGS technique is highly sensitive, and so if we can expand that and validate it in T-ALL, that would be highly useful because that makes up in the young adult population up to 30% of our patients. And so I think that that will be important. I don’t know of additional new techniques. There are these digital droplet PCR assays that can be implemented potentially for very high-risk subsets like the KMT2A rearranged ALL...
I think the NGS technique is highly sensitive, and so if we can expand that and validate it in T-ALL, that would be highly useful because that makes up in the young adult population up to 30% of our patients. And so I think that that will be important. I don’t know of additional new techniques. There are these digital droplet PCR assays that can be implemented potentially for very high-risk subsets like the KMT2A rearranged ALL. I know there are a number of groups working on that sort of approach that have not yet been completely validated, although validation studies are ongoing for that. So I think some of the digital droplet PCR for specific fusions will be useful, and then NGS as a broad stroke for most patients with ALL. At this moment, high sensitivity flow cytometry for MRD, I would say, is still the standard of care although many patients with T-ALL probably have robust markers that can be tracked but it’s just not quite as it’s not a hundred percent validated yet and it’s not yet FDA approved in the United States for monitoring MRD.
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