Locoregional CAR T cells for children with CNS tumors: Clinical procedure and catheter safety

Nicholas A. Vitanza(Seattle Children's Hospital), Rebecca Ronsley(Seattle Children's Hospital), Michelle Choe(Seattle Children's Hospital), Casey Henson(Seattle Children's Hospital), Mandy Breedt(Seattle Children's Hospital), Adriel Barrios-Anderson(Seattle Children's Hospital), Amy Wein(Seattle Children's Hospital), Christopher Brown(Seattle Children's Hospital), Adam Beebe(Seattle Children's Hospital), Ada Kong(Seattle Children's Hospital), Danielle Kirkey(Seattle Children's Hospital), Brittany M. Lee(Seattle Children's Hospital), Sarah Leary(Seattle Children's Hospital), Erin Crotty(Seattle Children's Hospital), Corrine Hoeppner(Seattle Children's Hospital), Susan Holtzclaw(Seattle Children's Hospital), Ashley Wilson, Joshua A. Gustafson, Jessica Foster(Children's Hospital of Philadelphia), Jeffrey J. Iliff(University of Washington), Hannah E. Goldstein(Seattle Children's Hospital), Samuel R. Browd(Seattle Children's Hospital), Amy Lee(Seattle Children's Hospital), Jeffrey G. Ojemann(Seattle Children's Hospital), Navin Pinto(Seattle Children's Hospital), Juliane Gust(Seattle Children's Hospital), Rebecca Gardner(Seattle Children's Hospital), Michael C. Jensen, Jason S. Hauptman(Seattle Children's Hospital), Julie R. Park(Seattle Children's Hospital)
Neoplasia
January 2, 2023
Cited by 32Open Access
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Abstract

Central nervous system (CNS) tumors are the most common solid malignancy in the pediatric population. Based on adoptive cellular therapy's clinical success against childhood leukemia and the preclinical efficacy against pediatric CNS tumors, chimeric antigen receptor (CAR) T cells offer hope of improving outcomes for recurrent tumors and universally fatal diseases such as diffuse intrinsic pontine glioma (DIPG). However, a major obstacle for tumors of the brain and spine is ineffective T cell chemotaxis to disease sites. Locoregional CAR T cell delivery via infusion through an intracranial catheter is currently under study in multiple early phase clinical trials. Here, we describe the Seattle Children's single-institution experience including the multidisciplinary process for the preparation of successful, repetitive intracranial T cell infusion for children and the catheter-related safety of our 307 intracranial CAR T cell doses.


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