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

被引:11
作者
Nielsen, Morten [1 ]
Monberg, Tine [1 ]
Sundvold, Vibeke [2 ]
Albieri, Benedetta [1 ]
Hovgaard, Dorrit [3 ]
Petersen, Michael Mork [3 ]
Krarup-Hansen, Anders [4 ]
Met, Oezcan [1 ,5 ]
Camilio, Ketil [2 ]
Clancy, Trevor [6 ]
Stratford, Richard [6 ]
Sveinbjornsson, Baldur [2 ]
Rekdal, Oystein [2 ]
Junker, Niels [4 ]
Svane, Inge Marie [1 ,7 ]
机构
[1] Copenhagen Univ Hosp, Natl Ctr Canc Immune Therapy CCIT DK, Dept Oncol, Herlev, Denmark
[2] Lytix Biopharm, Oslo, Norway
[3] Copenhagen Univ Hosp, Dept Orthoped Surg, Rigshosp, Copenhagen, Denmark
[4] Herlev & Gentofte Hosp, Dept Oncol, Herlev, Denmark
[5] Tech Univ Denmark, Dept Hlth Technol, Lyngby, Denmark
[6] NEC Oncoimmun, Oslo, Norway
[7] Copenhagen Univ Hosp, Herlev Hosp, Natl Ctr Canc Immune Therapy CCIT DK, Dept Oncol, Borgmester Ib Juuls Vej 13, DK-2730 Herlev, Denmark
来源
ONCOIMMUNOLOGY | 2024年 / 13卷 / 01期
关键词
Adoptive cell therapy; immunotherapy; LTX-315; soft tissue sarcoma; T-cell therapy; tumor infiltrating lymphocytes; COMPLETE REGRESSION; COMPLETE RESPONSES; ONCOLYTIC PEPTIDE; IMMUNOTHERAPY; MELANOMA; EXPRESSION; INFECTION; CANCER;
D O I
10.1080/2162402X.2023.2290900
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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
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页数:11
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