Most of the studies that have been done in this population are actually based on clinical trials. So the patients that have been enrolled are actually selected patients. What we have done here in this observational study, so this is real-world data, we wanted to better understand what is short-term patient-reported toxicity. When I’m saying short-term, I’m referring to basically 10 days after infusion, and we wanted to see the prevalence of toxicity reported by these patients...
Most of the studies that have been done in this population are actually based on clinical trials. So the patients that have been enrolled are actually selected patients. What we have done here in this observational study, so this is real-world data, we wanted to better understand what is short-term patient-reported toxicity. When I’m saying short-term, I’m referring to basically 10 days after infusion, and we wanted to see the prevalence of toxicity reported by these patients. So we have seen that the prevalence is very high, much more than is actually reported in the literature. And but there are no differences compared to among different types of CAR T-cell products, so I guess this is an encouraging message for the hematology community. And we have seen also that the type of CAR T-cell product doesn’t have an impact on short-term quality of life. We don’t know yet what is the impact, if there is an impact, of different products in terms of long-term quality of life outcomes. We’re going to see this in future research.
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