Calibrated CAR Signaling Enables Low-Dose Therapy in Large B-Cell Lymphoma

Author:

Park Jae1ORCID,Palomba M.Lia1ORCID,Perica Karlo1,Devlin Sean2ORCID,Shah Gunjan1,Dahi Parastoo1,Lin Richard1ORCID,Salles Gilles3ORCID,Scordo Michael1,Nath Karthik1,Valtis Yannis1,Lynch Alec1,Cathcart Elizabeth4,Zhang Honglei1,Schöder Heiko5,Leithner Doris1,Liotta Kelly1,Yu Alina1,Stocker Kelsey1,Li Jia6,Dey Agnish6,Sellner Leopold7,Singh Reshma6,Sundaresan Varsha7,Zhao Faye6,Mansilla-Soto Jorge8,He Changhao9,Meyerson Joel9,Hosszu Kinga1ORCID,McAvoy Devin1,Wang Xiuyan,Riviere Isabelle1,Sadelain Michel1ORCID

Affiliation:

1. Memorial Sloan Kettering Cancer Center

2. MSKCC

3. Memorial Sloan Kettering Cancer Center, New York, USA

4. Memorial Sloan Ketterning Cancer Center

5. Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY

6. Takeda Development Center Americas, Inc

7. Takeda Development Center America Inc.

8. Moffitt

9. Weill Cornell Medical College

Abstract

Abstract

We designed a CD19-targeted CAR comprising a calibrated signaling module, termed 1XX, that differs from that of conventional CD28/CD3z and 4-1BB/CD3z CARs. Here we report the first-in-human, phase 1 clinical trial of 19(T2)28z-1XX CAR T cells in relapsed/refractory large B-cell lymphoma. We hypothesized that 1XX CAR T cells may be effective at low doses and investigated 4 doubling dose levels starting from 25x106 CAR T cells. The overall response rate (ORR) was 82% and complete response (CR) rate 71% in the entire cohort (n=28) and 88% ORR and 75% CR in 16 patients treated at 25x106. With the median follow‐up of 24 months, the 1-year EFS was 61% (95% CI: 45-82%). Overall, grade ≥3 CRS and ICANS rates were low at 4% and 7%. The calibrated potency of the 1XX CAR affords excellent efficacy at low cell doses and may benefit the treatment of other hematological malignancies, solid tumors and autoimmunity.

Publisher

Springer Science and Business Media LLC

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