1478 A phase I study of personalized adoptive TCR T cell therapy in patients with solid tumors: safety, efficacy, and T cell trafficking to tumors of non-virally gene edited T cells
- Creators
- Foy, Susan
- Jacoby, Kyle
- Bota, Daniela
- Hunter, Theresa
- Schoenfeld, Adam
- Pan, Zheng
- Stawiski, Eric
- Ma, Yan
- Lu, William
- Peng, Songming
- Wang, Clifford
- Yuen, Benjamin
- Dalmas, Olivier
- Heeringa, Katharine
- Sennino, Barbara
- Conroy, Andy
- Bethune, Michael
- Mende, Ines
- White, William
- Kukreja, Monica
- Gunturu, Swetha
- Humphrey, Emily
- Hussaini, Adeel
- An, Duo
- Quach, Boi
- Ng, Alphonsus
- Lu, Yue
- Smith, Chad
- Campbell, Katie
- Anaya, Daniel
- Skrdlant, Lindsey
- Huang, Eva
- Mendoza, Ventura
- Mathur, Jyoti
- Dengler, Luke
- Purandare, Bhamini
- Moot, Robert
- Yi, Michael
- Funke, Roel
- Sibley, Alison
- Stallings-Schmitt, Todd
- Oh, David
- Chmielowski, Bartosz
- Abedi, Mehrdad
- Yuan, Yuan
- Sosman, Jeff
- Lee, Sylvia
- Williams, Claire
- Kim, Sean
- Keefe, Matthwe
- Leon, Michael
- Kim, Youngmi
- Reeves, Jason
- Goldman, Wes
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Baltimore, David
- Heath, James
- Franzusoff, Alex
- Ribas, Antoni
- Rao, Arati
- Mandl, Stefanie
Abstract
Background: NeoTCR-P1 is a personalized autologous T cell therapy for treatment of patients with solid tumors. Neoantigen-specific T cell receptors (neoTCRs) were isolated from the patients' own circulating CD8 T cells using the imPACT Isolation Technology®, followed by non-viral precision genome engineering into an autologous apheresis product for infusion back into the patient. Methods: This phase 1 trial is a first-in-human, multi-center, dose-escalation study to evaluate the safety, tolerability, and manufacturing feasibility of NeoTCR-P1 alone or in combination with IL-2 in solid tumors. Patients with TCRs identified at screening and meeting eligibility criteria underwent apheresis to manufacture personalized NeoTCR-P1 cell product. Lymphodepleted patients received a single dose of up-to-three distinct NeoTCR cell products at dose levels of 0.4, 1.2, or 4×10⁹ NeoTCR-edited T cells. Pre- and post-treatment blood and biopsy samples were collected to evaluate NeoTCR-P1 pharmacokinetics, tumor trafficking, signs of T cell engagement or potential mechanisms of resistance. Results: Sixteen patients were infused with NeoTCR-P1 T cells including patients with MSS-colorectal cancer (11), breast cancer (2), ovarian cancer (1), melanoma (1), or non-small cell lung cancer (1). Four of the sixteen patients were treated with NeoTCR-P1 + IL-2. Two patients experienced toxicities associated with NeoTCR-P1 cell infusions: a grade 1 CRS and a grade 2 ICANS. Five patients had stable disease as their best response at their first tumor assessment (day 28). NeoTCR+ T cells detected in the peripheral blood had an average peak of 3.6% (range 0.9-7.3%) for DL1, 11.7% (7.7-20.8%) for DL2, and 19.8% (12.0-37.3%) for DL3. Increases in NeoTCR T cells were observed at higher dose levels, stronger lymphodepletion, or higher gene editing rates of the infused product. Eight post-infusion biopsies were available for sequencing and imaging analysis; 17 of 22 neoTCR-T cells were detected in post-infusion biopsies with 12 neoTCRs among the top 4% of CDR3 sequences detected. The targeted neoantigens were detected in 7 of 8 post-treatment biopsies (15 of 22 targets), and personalized ctDNA confirmed targeting of a predicted sub-clonal mutation. An APOBEC signature and HLA-LOH were identified as potential mechanisms of resistance. By single-cell, spatial molecular imaging, neoTCR-T cells were visualized in post-treatment biopsies and found to differentially express potential markers of engagement. Conclusions: This study demonstrates the feasibility of isolating and manufacturing NeoTCR-T cells using non-viral precision genome engineering, the safety of infusing up-to-three gene edited NeoTCR-T cell products, and T cell persistence and trafficking to a variety of solid tumors.
Additional Information
© Author(s) (or their employer(s)) 2022. No commercial re-use.Additional details
- Eprint ID
- 121170
- Resolver ID
- CaltechAUTHORS:20230425-250392700.4
- Created
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2023-06-15Created from EPrint's datestamp field
- Updated
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2023-06-15Created from EPrint's last_modified field
- Caltech groups
- Division of Biology and Biological Engineering