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Re: poorgradstudent post# 202498

Sunday, 07/10/2016 10:08:44 AM

Sunday, July 10, 2016 10:08:44 AM

Post# of 257440

At first blush this sound analogous to how we make mutant / resistant strains in the lab



and pulsing antibiotics is a great way to induce resistance. point taken. Whether or not such a strategy will result in resistant leukemic cells is a theoretical risk

If you are actually lowering disease burden, why not let the CAR-Ts persist?



If you have an AE that is correlated to dx burden like cytokine storm then it could abate as the disease is eradicated without the need for turning off the T cells, but there still could be cases where a reprieve could be the safest course of action

Not trying to be combative or obtuse, just trying to reason out the setting where an On/Off CAR-T would be necessary



no offense taken - you make valid points about how an on/off is by no means a panacea and may have limited usefulness, especially once there is more experience w prophylaxis and management of the AEs. However I also think it is premature to be totally dismissive of the value of such switches

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