溶瘤病毒
医学
肉瘤
癌症
软组织肉瘤
临床试验
肿瘤科
内科学
免疫系统
免疫学
癌症研究
病理
作者
Yeting Qiu,Aijun Qin,Jun Ding,William Jia,Manu Singh,Yanal Murad,Qian Tan,Ganessan Kichenadasse
标识
DOI:10.3892/ol.2024.14377
摘要
Sarcoma is derived from mesenchymal neoplasms and has numerous subtypes, accounting for 1% of all adult malignancies and 15% of childhood malignancies. The prognosis of metastatic or recurrent sarcoma remains poor. The current study presents two cases of sarcoma enrolled in a phase I dose escalation trial for solid tumor, who had previously failed all standard therapies. These patients were treated with VG161, an immune‑stimulating herpes simplex virus type 1 oncolytic virus with payloads of IL‑12, IL‑15 and IL‑15 receptor α unit, and a programmed cell death 1 (PD‑1)/PD‑1 ligand 1 blocking peptide. Both cases demonstrated stable disease as the best response, accompanied by a noteworthy prolongation of progression‑free survival (11.8 months for chondrosarcoma and 11.9 months for soft tissue sarcoma, respectively) at a dose of 2.5x108 PFU/cycle. In addition, the treatment led to the activation of anti‑cancer immunity, as evident from cytokine, lymphocyte subset and related pathway analyses of peripheral blood and/or tumor biopsy samples. These promising results suggest that VG161 monotherapy holds promise as an effective treatment for sarcoma and warrants further investigation through clinical trials. The two reported patients were part of a phase I clinical trial conducted and registered on the Australian New Zealand Clinical Trials Registry in Australia (registration no. ACTRN12620000244909; registration date, 26 February, 2020).
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