Article
Author: Pichavant, Mina ; Bendall, Sean ; Duong, Vandon ; Derdak, Joanne ; Highfill, Steven L ; Reynolds, Warren ; Dombi, Eva ; Anbunathan, Hima ; Kaplan, Rosandra N ; Ong, Claire ; Maecker, Holden ; Van Nostrand, Stephen ; Hedrick, Catherine C ; Wu, Catherine J ; Bernstein, Donna ; Sotillo, Elena ; Mackall, Crystal L ; Jhaveri, Aashna ; Liu, Yang ; Ramakrishna, Sneha ; Baskar, Reema ; Klicka-Skeels, Jacquelyn ; Moravec, Radim ; Biswas, Roshni ; Lindsay, James ; Murty, Tara ; Michor, Franziska ; Carbonell, Amanda ; Sahaf, Bita ; Alimadadi, Ahmad ; Turkbey, Baris ; Yu, Joyce ; Zhang, Hua ; Merchant, Melinda ; Gutierrez, Norma A ; Stroncek, David ; Segal, Julia E ; Kaczanowska, Sabina ; Harmon, Stephanie A ; Contreras, Cristina F ; Altreuter, Jennifer ; Glod, John ; Duault, Caroline ; Subrahmanyam, Priyanka B
Chimeric antigen receptor T cells (CAR-Ts) have remarkable efficacy in liquid tumors, but limited responses in solid tumors. We conducted a Phase I trial (NCT02107963) of GD2 CAR-Ts (GD2-CAR.OX40.28.z.iC9), demonstrating feasibility and safety of administration in children and young adults with osteosarcoma and neuroblastoma. Since CAR-T efficacy requires adequate CAR-T expansion, patients were grouped into good or poor expanders across dose levels. Patient samples were evaluated by multi-dimensional proteomic, transcriptomic, and epigenetic analyses. T cell assessments identified naive T cells in pre-treatment apheresis associated with good expansion, and exhausted T cells in CAR-T products with poor expansion. Myeloid cell assessment identified CXCR3+ monocytes in pre-treatment apheresis associated with good expansion. Longitudinal analysis of post-treatment samples identified increased CXCR3- classical monocytes in all groups as CAR-T numbers waned. Together, our data uncover mediators of CAR-T biology and correlates of expansion that could be utilized to advance immunotherapies for solid tumor patients.