Oncolytic virotherapy stimulates anti‑tumor immune response and demonstrates activity in advanced sarcoma: Report of two cases.

IF 2.5 4区 医学 Q3 ONCOLOGY Oncology Letters Pub Date : 2024-04-03 DOI:10.3892/ol.2024.14377
Yeting Qiu, Aijun Qin, Ronghua Zhao, Jun Ding, William Wei-Guo Jia, Manu Singh, Yanal Murad, Qian Tan, Ganessan Kichenadasse
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Abstract

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 2.5×108 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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肿瘤溶解病毒疗法可刺激抗肿瘤免疫反应,对晚期肉瘤具有活性:两个病例的报告。
肉瘤源于间质肿瘤,有许多亚型,占所有成人恶性肿瘤的 1%,占儿童恶性肿瘤的 15%。转移性或复发性肉瘤的预后仍然很差。本研究介绍了两例参加实体瘤 I 期剂量递增试验的肉瘤患者,这些患者曾接受过所有标准疗法,但均告失败。这些患者接受了VG161治疗,VG161是一种免疫刺激型单纯疱疹病毒1型溶瘤病毒,含有IL-12、IL-15和IL-15受体α单位有效载荷,以及程序性细胞死亡1(PD-1)/PD-1配体1阻断肽。两个病例的最佳反应都是病情稳定,同时在剂量为2.5×108 PFU/周期时,无进展生存期显著延长(软骨肉瘤为11.8个月,软组织肉瘤为11.9个月)。此外,对外周血和/或肿瘤活检样本进行的细胞因子、淋巴细胞亚群和相关通路分析显示,该疗法还能激活抗癌免疫。这些令人鼓舞的结果表明,VG161 单药疗法有望成为肉瘤的有效治疗方法,值得通过临床试验进一步研究。报道中的两名患者是在澳大利亚进行的 I 期临床试验的一部分,并在澳大利亚新西兰临床试验注册中心进行了注册(注册号 ACTRN12620000244909;注册日期 2020 年 2 月 26 日)。
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来源期刊
Oncology Letters
Oncology Letters ONCOLOGY-
CiteScore
5.70
自引率
0.00%
发文量
412
审稿时长
2.0 months
期刊介绍: Oncology Letters is a monthly, peer-reviewed journal, available in print and online, that focuses on all aspects of clinical oncology, as well as in vitro and in vivo experimental model systems relevant to the mechanisms of disease. The principal aim of Oncology Letters is to provide the prompt publication of original studies of high quality that pertain to clinical oncology, chemotherapy, oncogenes, carcinogenesis, metastasis, epidemiology and viral oncology in the form of original research, reviews and case reports.
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