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

Meenakshi Hegde(Houston Methodist), Sujith K. Joseph(Houston Methodist), Farzana Pashankar(Yale University), Christopher DeRenzo(Houston Methodist), Khaled Sanber(Houston Methodist), Shoba A. Navai(Houston Methodist), Tiara T. Byrd(Houston Methodist), John Hicks(Baylor College of Medicine), Mina L. Xu(Yale University), Claudia Gerken(Houston Methodist), Mamta Kalra(Houston Methodist), Catherine Robertson(Houston Methodist), Huimin Zhang(Houston Methodist), Ankita Shree(Houston Methodist), Birju Mehta(Houston Methodist), Olga Dakhova(Houston Methodist), Vita S. Salsman(Houston Methodist), Bambi Grilley(Houston Methodist), Adrian P. Gee(Houston Methodist), Gianpietro Dotti(University of North Carolina at Chapel Hill), Helen E. Heslop(Houston Methodist), Malcolm K. Brenner(Houston Methodist), Winfried S. Wels(Goethe University Frankfurt), Stephen Gottschalk(Houston Methodist), Nabil Ahmed(Houston Methodist)
Nature Communications
July 15, 2020
Cited by 164Open Access
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Abstract

Refractory 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.


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