Immune modulation after Toca 511 and Toca FC treatment of colorectal cancer patients.

Authors

null

Gerald Steven Falchook

Sarah Cannon Research Institute, Denver, CO

Gerald Steven Falchook , Jordi Rodon Ahnert , Shree Venkat , Arthur Donahue , Peder Horner , Amber Thomassen , William Accomando , Maria Rodriguez-Aguirre , Cornelia Bentley , Daniel Hogan , Derek Ostertag , Sharon Yavrom , Thian Kheoh , Douglas J. Jolly , Harry E. Gruber , Jolene Shorr , Jaime R. Merchan

Organizations

Sarah Cannon Research Institute, Denver, CO, The University of Texas MD Anderson Cancer Center, Houston, TX, University of Miami Miller School of Medicine, Sylvester Comprehensive Cancer Center, Miami, FL, Sarah Cannon Research Institute at HealthONE, Denver, CO, University of Miami-Sylvester Comprehensive Cancer Center, Miami, FL, Tocagen Inc., San Diego, CA, Tocagen, Inc., San Diego, CA, Tocagen, San Diego, CA, Janssen Research and Development, LLC, San Diego, CA, University of Miami, Miami, FL

Research Funding

Pharmaceutical/Biotech Company
Tocagen

Background: Toca 511 (vocimagene amiretrorepvec) is a cancer-selective, retroviral replicating vector encoding yeast cytosine deaminase that converts 5-fluorocytosine (5-FC) into 5-fluorouracil in the tumor microenvironment (TME). In animal models, Toca 511 and 5-FC kill dividing cancer and nearby immunosuppressive cells, leading to antitumor immune activity. A Phase 1 study of Toca 511 & Toca FC (extended-release 5-FC) in patients with recurrent high grade glioma revealed results consistent with this proposed mechanism. A Phase 3 trial is ongoing. Methods: Toca 6 (NCT02576665) is a Phase 1b, single-arm, multicenter study designed to investigate immunological changes after Toca 511 & Toca FC treatment in patients with advanced solid tumors, including colorectal cancer (CRC). Patients received intravenous (IV) Toca 511 for 3 days, and underwent biopsy of metastatic tumor before and ~ 4 weeks after starting oral Toca FC. Toca FC was repeated every 4-6 weeks. Peripheral blood mononuclear cells and tumor biopsies were evaluated for treatment related immune responses. Results: 17 CRC patients with a median 5 lines of prior chemotherapy were enrolled. At last data cut-off, 9 patients were alive and the median overall survival was 9.4 months. A patient receiving concomitant panitumumab had a partial response. IV Toca 511 led to viral expression in tumor, which decreased post-Toca FC while maintaining a reservoir of virus in the remaining tumor. T cells shifted from naïve to effector phenotypes, CD4 memory T cells expanded, and/or B cells increased after Toca FC treatment in 36% of patients. Marked changes in tumor infiltrating cells (CD11b myeloid cells, Tregs, exhausted T cells and CD8 T cells) occurred after Toca FC treatment. Treatment has been generally well tolerated. We also plan to report insights gained from RNA analysis of TME and update on clinical finding. Conclusions: Clinical data suggest a signal of activity in these heavily pretreated CRC patients warranting further exploration. IV Toca 511 administration showed viral infection of CRC metastatic tumor. Toca 511 & Toca FC may be associated with T cell mediated immune activity in peripheral blood and metastatic tumor, consistent with pre-clinical data in multiple tumor types. Clinical trial information: NCT02576665

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Abstract Details

Meeting

2020 Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Anal and Colorectal Cancer

Track

Colorectal Cancer,Anal Cancer

Sub Track

Translational Research

Clinical Trial Registration Number

NCT02576665

Citation

J Clin Oncol 38, 2020 (suppl 4; abstr 186)

Abstract #

186

Poster Bd #

J6

Abstract Disclosures