Panelists discuss how CAR T monitoring requirements have evolved from initially conservative inpatient approaches to more flexible outpatient strategies, exploring ways to reduce the burden of mandatory 30-plus-day proximity requirements while maintaining patient safety and improving treatment accessibility.
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CAR T therapy monitoring requirements significantly impact patient quality of life and treatment accessibility. Current protocols typically require patients to remain within a specified radius of treatment centers for 30-plus-days post infusion, creating substantial socioeconomic barriers. This requirement forces patients and caregivers to pause their lives, potentially requiring extended time off work and temporary relocation, which differs dramatically from traditional chemotherapy schedules where patients receive treatment and return home the same day.
Treatment approaches vary among institutions, with some routinely admitting all CAR T patients while others have transitioned to outpatient management for products like liso-cel. The choice between inpatient and outpatient administration depends on institutional comfort levels, available resources, and specific product characteristics. Many institutions are now treating low-grade toxicities in outpatient settings, admitting patients only when adverse events occur.
The critical question emerging from clinical experience is whether all current monitoring requirements remain necessary throughout the entire 30-day period. While early post–CAR T monitoring is essential for detecting cytokine release syndrome and neurological toxicities, many patients by day 22 have passed the high-risk period and may only require routine supportive care (transfusions, infection monitoring) that community oncologists routinely provide. This evolution in understanding suggests opportunities to modify monitoring protocols while maintaining safety standards, potentially improving access by reducing the duration of required proximity to CAR T centers.
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