Key considerations for advancing chimeric antigen receptor (CAR) T-cell therapy for systemic lupus erythematosus (SLE): a multi-partner/disciplinary working group perspective.
СтатьяОбзорПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Hsieh Elena W Y, Chung James B, Amin Afsah, Askanase Anca D, Bartok Beatrix, Brunetta Paul, Carrasco-Alfonso Marlene J, Coney Cindy, Cooper Jennifer C, Dall'Era Maria, Delev Nikolay, Eldred Ann, Furie Richard A, Garces Sandra, Groover Katie, Harrington Monica, Hogan Jonathan J, Imperato Gavin H, Jackson Meredith, Jackson Shaun W, Jongco Artemio M, Karis Elaine, Koegel Ashley, König Maximilian F, Koretzky Gary, Kumar Vijay, Morand Eric, Payne Aimee S, Popat Vaishali, Rizvi Naiyer, Rohan Patricia, Sadelain Michel, Schett Georg, Singh Aman P, van Vollenhoven Ronald F, Zack Debra, Lupus ABC CAR T Working Group
Аннотация
Early data have shown the potential of chimeric antigen receptor (CAR) T-cell therapies to expand the therapeutic landscape in systemic lupus erythematosus (SLE). While many CAR T-cell therapy learnings can be drawn from the experience of this modality in oncology, key questions remain regarding clinical development considerations unique to lupus. To assess and discuss these issues, the Lupus Accelerating Breakthroughs Consortium, a public-private partnership, convened a multi-partner working group to collect the diverse perspectives of academics/clinicians (including rheumatologists and oncologists), industry representatives (including SLE as well as CAR T-cell clinical development experts), regulators and people living with lupus on this potentially ground-breaking therapy. The working group considered the risk/benefit considerations for eligibility criteria in lupus, early-phase dosing and dose-limiting toxicity challenges, incorporation of comparator arms in late-phase registrational trial design, SLE-specific issues in conditioning therapy and immune monitoring and the limitations of SLE pre-clinical models for studying cell therapies. The key future 'calls to action' for the field include the need for well-defined severity/refractoriness-based eligibility criteria, the need for long-term monitoring infrastructure and the need for educational and logistical support for rheumatologists and patients.