Tumor response and endogenous immune reactivity after administration of HER2 CAR T cells in a child with metastatic rhabdomyosarcoma

Author:

Hegde MeenakshiORCID,Joseph Sujith K.,Pashankar FarzanaORCID,DeRenzo Christopher,Sanber Khaled,Navai ShobaORCID,Byrd Tiara T.,Hicks John,Xu Mina L.,Gerken Claudia,Kalra Mamta,Robertson Catherine,Zhang Huimin,Shree Ankita,Mehta Birju,Dakhova Olga,Salsman Vita S.,Grilley Bambi,Gee Adrian,Dotti Gianpietro,Heslop Helen E.,Brenner Malcolm K.,Wels Winfried S.,Gottschalk StephenORCID,Ahmed NabilORCID

Abstract

AbstractRefractory metastatic rhabdomyosarcoma is largely incurable. Here we analyze the response of a child with refractory bone marrow metastatic rhabdomyosarcoma to autologous HER2 CAR T cells. Three cycles of HER2 CAR T cells given after lymphodepleting chemotherapy induces remission which is consolidated with four more CAR T-cell infusions without lymphodepletion. Longitudinal immune-monitoring reveals remodeling of the T-cell receptor repertoire with immunodominant clones and serum autoantibodies reactive to oncogenic signaling pathway proteins. The disease relapses in the bone marrow at six months off-therapy. A second remission is achieved after one cycle of lymphodepletion and HER2 CAR T cells. Response consolidation with additional CAR T-cell infusions includes pembrolizumab to improve their efficacy. The patient described here is a participant in an ongoing phase I trial (NCT00902044; active, not recruiting), and is 20 months off T-cell infusions with no detectable disease at the time of this report.

Funder

EIF | Stand Up To Cancer

American Association for Cancer Research

U.S. Department of Health & Human Services | NIH | National Cancer Institute

Alex's Lemonade Stand Foundation for Childhood Cancer

Cancer Prevention and Research Institute of Texas

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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