Consensus recommendations for CAR T-cell administration in adult acute lymphoblastic leukemia: a modified Delphi study.
СтатьяConsensus StatementНазвание и аннотация: Перевод в очереди
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Muffly Lori, Frey Noelle V, Roloff Gregory W, Park Jae A, Dholaria Bhagirathbhai, Advani Anjali, Bachanova Veronika, Cassaday Ryan D, Daunov Michael, Dykes Kaitlyn C, Gatell Vivian Irizarry, Grunwald Michael R, Hilal Talal, Hill LaQuisa C, Jamy Omer, Kota Vamsi K, Kumaran Muthu Veera, Lin Chenyu, Logan Aaron C, Luskin Marlise R, O'Dwyer Kristen M, Oliai Caspian, Oluwole Olalekan O, Sasine Joshua P, Schwartz Marc S, Solh Melhem M, Stock Wendy, Tsai Stephanie B, Ulrickson Matthew, Vasu Sumithira, Wang Eunice S, Yalniz Fevzi Firat, Strickland Stephen A, Leonard Jessica T, Shah Bijal D, Aldoss Ibrahim
Аннотация
The use of chimeric antigen receptor (CAR) T-cell therapy is increasing for adult B-cell acute lymphoblastic leukemia (B-ALL), with 3 CD19 CAR T-cell products commercially available. Several key clinical questions related to best practices for CAR T-cell administration in this population exist, and limited prospective randomized trials have been conducted to fill these knowledge gaps. Thus, to help guide clinical practice, we conducted a modified Delphi study to develop and validate consensus recommendations on the administration of commercially available CAR T-cell therapy for adults with B-ALL. Consensus panelists (n = 9) included principal investigators (PIs) from Real World Outcomes Collaborative of CAR T-Cell Therapy in Adult ALL (ROCCA) consortium sites and were selected based on expertise and CAR T-cell center volume. Final panel consensus recommendations were distributed for rating by the remaining PIs from ROCCA consortium sites, which served as the validation group (n = 27). Consensus topics included patient selection, bridging and pre-CAR T-cell leukemia staging, lymphodepletion, and CAR T-cell treatment setting, specific toxicity prevention and management, post-CAR T-cell response assessment and disease monitoring, and the role of consolidation and/or maintenance therapies after CAR T-cell therapy. Initially, 58 recommendation statements were evaluated for consensus. After 2 panel meetings, a total of 34 statements achieved consensus rating among the expert panel. After rating by the validation group, all but 1 recommendation statement continued to meet consensus, for a total of 33 consensus recommendation statements on the administration of CAR T-cell therapy in adult B-ALL.