Tisagenlecleucel in Children and Young Adults with B-Cell Lymphoblastic Leukemia

Shannon L. Maude(Children's Hospital of Philadelphia), Theodore W. Laetsch(Center for Cancer and Blood Disorders), Jochen Buechner(Université de Montréal), Susana Rives(Hospital Sant Joan de Déu Barcelona), Michael Boyer(University of Utah), Henrique Bittencourt(Centre Hospitalier Universitaire Sainte-Justine), Peter Bader(Goethe University Frankfurt), Michael R. Verneris(University of Minnesota), Heather E. Stefanski(University of Minnesota), Gary D. Myers(Children's Mercy Hospital), Muna Qayed(Center for Cancer and Blood Disorders), Barbara De Moerloose, Hidefumi Hiramatsu(Kyoto University), Krysta Schlis(Stanford University), Kara L. Davis(Stanford University), Paul L. Martin(Duke Medical Center), Eneida R. Nemecek(Oregon Health & Science University), Gregory A. Yanik(C. S. Mott Children's Hospital), Christina Peters(St Anna Children's Hospital), André Baruchel(Université Paris Cité), Nicolas Boissel(Délégation Paris 7), Françoise Méchinaud(Royal Children's Hospital), Adriana Balduzzi(University of Milano-Bicocca), Joerg Krueger(Hospital for Sick Children), Carl H. June(University of Pennsylvania), Bruce L. Levine(University of Pennsylvania), Patricia A. Wood(Novartis (Switzerland)), Tetiana Taran(Novartis (Switzerland)), Mimi Leung(Novartis (Switzerland)), Karen T. Mueller(Novartis Institutes for BioMedical Research), Yiyun Zhang(Novartis (Switzerland)), Kapildeb Sen(Novartis (Switzerland)), David Lebwohl(Novartis (Switzerland)), Michael A. Pulsipher(Children's Hospital of Los Angeles), Stephan A. Grupp(University of Pennsylvania)
New England Journal of Medicine
January 31, 2018
Cited by 5,580Open Access
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Abstract

BACKGROUND: In a single-center phase 1-2a study, the anti-CD19 chimeric antigen receptor (CAR) T-cell therapy tisagenlecleucel produced high rates of complete remission and was associated with serious but mainly reversible toxic effects in children and young adults with relapsed or refractory B-cell acute lymphoblastic leukemia (ALL). METHODS: We conducted a phase 2, single-cohort, 25-center, global study of tisagenlecleucel in pediatric and young adult patients with CD19+ relapsed or refractory B-cell ALL. The primary end point was the overall remission rate (the rate of complete remission or complete remission with incomplete hematologic recovery) within 3 months. RESULTS: For this planned analysis, 75 patients received an infusion of tisagenlecleucel and could be evaluated for efficacy. The overall remission rate within 3 months was 81%, with all patients who had a response to treatment found to be negative for minimal residual disease, as assessed by means of flow cytometry. The rates of event-free survival and overall survival were 73% (95% confidence interval [CI], 60 to 82) and 90% (95% CI, 81 to 95), respectively, at 6 months and 50% (95% CI, 35 to 64) and 76% (95% CI, 63 to 86) at 12 months. The median duration of remission was not reached. Persistence of tisagenlecleucel in the blood was observed for as long as 20 months. Grade 3 or 4 adverse events that were suspected to be related to tisagenlecleucel occurred in 73% of patients. The cytokine release syndrome occurred in 77% of patients, 48% of whom received tocilizumab. Neurologic events occurred in 40% of patients and were managed with supportive care, and no cerebral edema was reported. CONCLUSIONS: In this global study of CAR T-cell therapy, a single infusion of tisagenlecleucel provided durable remission with long-term persistence in pediatric and young adult patients with relapsed or refractory B-cell ALL, with transient high-grade toxic effects. (Funded by Novartis Pharmaceuticals; ClinicalTrials.gov number, NCT02435849 .).


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