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

阅读:2
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  0

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.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。