Safety, Efficacy, and Biological Data of T-Cell–Enabling Oncolytic Adenovirus TILT-123 in Advanced Solid Cancers from the TUNIMO Monotherapy Phase I Trial

Author:

Pakola Santeri A.1ORCID,Peltola Katriina J.2ORCID,Clubb James H.A.13ORCID,Jirovec Elise1ORCID,Haybout Lyna13ORCID,Kudling Tatiana V.1ORCID,Alanko Tuomo4ORCID,Korpisaari Riitta4ORCID,Juteau Susanna5ORCID,Jaakkola Marjut2ORCID,Sormunen Jorma4ORCID,Kemppainen Jukka4ORCID,Hemmes Annabrita6ORCID,Pellinen Teijo6ORCID,van der Heijden Mirte1ORCID,Quixabeira Dafne C.A.13ORCID,Kistler Claudia3ORCID,Sorsa Suvi13ORCID,Havunen Riikka13ORCID,Santos Joao M.13ORCID,Cervera-Carrascon Victor13ORCID,Hemminki Akseli123ORCID

Affiliation:

1. Cancer Gene Therapy Group, Translational Immunology Research Program, University of Helsinki, Helsinki, Finland. 1

2. Comprehensive Cancer Center, Helsinki University Hospital, Helsinki, Finland. 2

3. TILT Biotherapeutics Ltd., Helsinki, Finland. 3

4. Docrates Cancer Center, Helsinki, Finland. 4

5. Department of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. 5

6. Digital Microscopy and Molecular Pathology Unit, Institute for Molecular Medicine Finland, Helsinki, Finland. 6

Abstract

Abstract Purpose: TILT-123 (igrelimogene litadenorepvec) is an oncolytic adenovirus armed with TNFa and IL2, designed to induce T-cell infiltration and cytotoxicity in solid tumors. Patients and Methods: TUNIMO (NCT04695327) was a single-arm, multicenter phase I dose-escalation trial designed to assess the safety of TILT-123 in advanced solid cancers refractory to standard therapy. Patients received intravenous and intratumoral TILT-123. The primary endpoint was safety by adverse events (AE), laboratory values, vital signs, and electrocardiograms. Secondary endpoints included tumor response, pharmacokinetics, and predictive biomarkers. Results: Twenty patients were enrolled, with a median age of 58 years. Most prevalent cancer types included sarcomas (35%), melanomas (15%) and ovarian cancers (15%). No dose-limiting toxicities were observed. The most frequent treatment-related AEs included fever (16.7%), chills (13.0%), and fatigue (9.3%). Ten patients were evaluable for response on day 78 with RECIST 1.1, iRECIST or PET-based evaluation. The disease control rate by PET was 6/10 (60% of evaluable patients) and 2/10 by RECIST 1.1 and iRECIST(20%of evaluable patients). Tumor size reductions occurred in both injected and non-injected lesions. TILT-123 was detected in injected and non-injected tumors, and virus was observed in blood after intravenous and intratumoral injections. Treatment resulted in reduction of lymphocytes in blood, with concurrent lymphocyte increases in tumors, findings compatible with trafficking. Conclusions: TILT-123 was safe and able to produce antitumor effects in local and distant lesions in heavily pre-treated patients. Good tolerability of TILT-123 facilitates combination studies, several of which are ongoing (NCT04217473, NCT05271318, NCT05222932, and NCT06125197). See related commentary by Silva-Pilipich and Smerdou, p. 3649

Funder

Helsinki University Hospital Research funds

Cancer Foundation Finland

Jane and Aatos Erkko Foundation

Red Cross Blood Service

Sigrid Juselius Finland

TILT Biotherapeutics Oy

European Commision

Publisher

American Association for Cancer Research (AACR)

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