LTX-315 and adoptive cell therapy using tumor-infiltrating lymphocytes generate tumor specific T cells in patients with metastatic soft tissue sarcoma

• Published in: Oncoimmunology Vol. 13; no. 1; p. 2290900
• Main Authors: Nielsen, Morten, Monberg, Tine, Sundvold, Vibeke, Albieri, Benedetta, Hovgaard, Dorrit, Petersen, Michael Mørk, Krarup-Hansen, Anders, Met, Özcan, Camilio, Ketil, Clancy, Trevor, Stratford, Richard, Sveinbjornsson, Baldur, Rekdal, Øystein, Junker, Niels, Svane, Inge Marie
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 31-12-2024; Taylor & Francis Group
• Subjects: Adoptive cell therapy; Humans; immunotherapy; Immunotherapy, Adoptive - adverse effects; Immunotherapy, Adoptive - methods; LTX-315; Lymphocytes, Tumor-Infiltrating; Neoplasms, Second Primary; Original Research; Pilot Projects; Sarcoma - therapy; Soft Tissue Neoplasms - therapy; soft tissue sarcoma; T-cell therapy; T-Lymphocytes; tumor infiltrating lymphocytes; Adoptive cell therapy; soft tissue sarcoma; tumor infiltrating lymphocytes; LTX-315; immunotherapy; T-cell therapy
• ISSN: 2162-402X; 2162-4011; 2162-402X
• DOI: 10.1080/2162402X.2023.2290900

LTX-315 is an oncolytic peptide that elicits both local and systemic immune responses upon intratumoral injection. In the present pilot trial, we treated patients with metastatic soft tissue sarcoma with the combination of LTX-315 and adoptive T-cell therapy using in vitro expanded tumor-infiltrating lymphocytes. Six heavily pretreated patients were included in the trial and treated with LTX-315 of which four patients proceeded to adoptive T-cell therapy. Overall, the treatment was considered safe with only expected and manageable toxicity. The best overall clinical response was stable disease for 208 days, and in this patient, we detected tumor-reactive T cells in the blood that lasted until disease progression. In three patients T-cell reactivity against in silico predicted neoantigens was demonstrated. Additionally, de novo T-cell clones were generated and expanded in the blood following LTX-315 injections. In conclusion, this pilot study provides proof that it is feasible to combine LTX-315 and adoptive T-cell therapy, and that this treatment can induce systemic immune responses that resulted in stabilization of the disease in sarcoma patients with otherwise progressive disease. Further optimization of the treatment protocol is warranted to increase clinical activity. ClinicalTrials.gov Identifier: NCT03725605.