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Poster Display

51P - Immunological analysis of blood from patients with solid tumors treated with TILT-123, an oncolytic adenovirus encoding for tumor necrosis factor alpha (TNFa) and interleukin 2 (IL-2)

Date

08 Dec 2022

Session

Poster Display

Presenters

Santeri Pakola

Citation

Annals of Oncology (2022) 16 (suppl_1): 100101-100101. 10.1016/iotech/iotech100101

Authors

S. Pakola1, J.M. Santos2, V. Cervera-Carrascon2, C. Kistler2, S. Sorsa2, R. Havunen2, A. Hemminki2

Author affiliations

  • 1 University of Helsinki, Helsinki/FI
  • 2 TILT Biotherapeutics Ltd, Helsinki/FI

Resources

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Abstract 51P

Background

In recent years, cancer therapy has witnessed the successful development and clinical implementation of a wide array of tools to fight cancer, including, for example, monoclonal antibodies and adoptive cell therapies (ACT). Immunotherapies employing such tools to reinvigorate T-cells continue to change patient care by providing durable benefit in patients with advanced solid tumors. The latter is offset, however, by a large share of patients that present little response to immunotherapy, in part due to T-cell dysfunction. To overcome this issue, we constructed a chimeric oncolytic adenovirus (TILT-123; Ad5/3-E2F-D24-TNFa-IRES-IL2) capable of expressing tumor necrosis factor alpha (TNFa) and interleukin-2 (IL-2). The use of this agent in preclinical cancer models led to complete responses and favorable immunological effects, both as monotherapy or, in combination with immune checkpoint inhibitors and ACT using tumor-infiltrating lymphocytes (TIL) or chimeric antigen receptor T-cells.

Methods

Blood from patients enrolled in TILT-T115, a clinical study using TILT-123 as monotherapy in patients with injectable advanced solid tumors (NCT04695327), was collected at screening and during treatment, and peripheral blood mononuclear cells (PBMCs) and serum were extracted. Immunological effects were evaluated by detecting immune cell populations in PBMCs by flow cytometry, and by detecting cytokines in blood serum by a targeted multiplexed immuno-assay.

Results

Preliminary immunological data points at immune effects both in PBMCs and blood serum of patients undergoing treatment. Immunological data (e.g. flow cytometry and/or cytokine data) will be presented.

Conclusions

TILT-123 can induce systemic immunological effects supporting the continued development of the agent as cancer immunotherapy.

Clinical trial identification

NCT04695327 (first posted January 5, 2021).

Legal entity responsible for the study

TILT Biotherapeutics Ltd.

Funding

TILT Biotherapeutics Ltd.

Disclosure

J.M. Santos, V. Cervera-Carrascon, C. Kistler: Financial Interests, Institutional, Full or part-time Employment: TILT Biotherapeutics Ltd; Financial Interests, Personal, Stocks/Shares: TILT Biotherapeutics Ltd. S. Sorsa: Financial Interests, Personal, Stocks/Shares: TILT Biotherapeutics Ltd; Financial Interests, Institutional, Full or part-time Employment: TILT Biotherapeutics Ltd. R. Havunen: Financial Interests, Institutional, Full or part-time Employment: TILT Biotherapeutics Ltd. A. Hemminki: Financial Interests, Personal, Stocks/Shares: Targovax, TILT Biotherapeutics Ltd; Financial Interests, Institutional, Full or part-time Employment, CEO: TILT Biotherapeutics Ltd; Financial Interests, Institutional, Member of the Board of Directors: TILT Biotherapeutics Ltd. All other authors have declared no conflicts of interest.

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