Safety and efficacy of combined treatment with tumor-infiltrating lymphocytes and oncolytic adenovirus TILT-123 in metastatic melanoma

肿瘤浸润淋巴细胞联合溶瘤腺病毒TILT-123治疗转移性黑色素瘤的安全性和有效性

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作者:Tine J Monberg ,Santeri A Pakola ,Benedetta Albieri ,Eva Ellebaek ,Marco Donia ,Rikke L Eefsen ,Troels H Borch ,Tatiana V Kudling ,Torben Lorentzen ,Helle W Hendel ,Cecilie Vestergaard ,Cathrine Lorentzen ,Rikke B Holmstroem ,Victor Arias ,Amir Khammari ,Claudia Kistler ,João M Santos ,James H A Clubb ,Lyna Haybout ,Marie C W Westergaard ,Özcan Met ,Dafne C A Quixabeira ,Elise Jirovec ,Riikka Havunen ,Suvi Sorsa ,Victor Cervera-Carrascon ,Brigitte Dreno ,Akseli Hemminki ,Inge Marie Svane

Abstract

Tumor-infiltrating lymphocytes (TILs) are effective in the treatment of metastatic melanoma (MM), but toxicity limits its application. TILT-123 (igrelimogene litadenorepvec) is an oncolytic adenovirus producing interleukin-2 (IL-2) and tumor necrosis factor (TNF) upon replication. In this phase 1 trial, 17 patients with metastatic checkpoint inhibitor-resistant melanoma are treated with TILT-123 and TILs without preconditioning chemotherapy or postconditioning IL-2. The treatment is safe and feasible. According to computed tomography (CT), the objective response rate is 11.7% (2/17) and disease control is observed in 35% (6/17), including a partial response lasting >8 months and a durable complete response in a mucosal melanoma patient. According to positron emission tomography (PET), disease control is observed in 7/15 (47%) with minor or partial responses in 4/15 (27%). In the initial TILT-123 monotherapy phase of the trial, disease control is observed in 6/17 (35%) and 10/16 (63%) in CT and PET, respectively. The study demonstrates good tolerability and preliminary efficacy.

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