Cancer Gene Therapy Group Department of Pathology and Transplantation Laboratory, Haartman Institute, University of Helsinki, Helsinki, Finland.
Int J Cancer. 2014 Aug 1;135(3):720-30. doi: 10.1002/ijc.28696. Epub 2014 Jan 10.
Sarcomas are a relatively rare cancer, but often incurable at the late metastatic stage. Oncolytic immunotherapy has gained attention over the past years, and a wide range of oncolytic viruses have been delivered via intratumoral injection with positive safety and promising efficacy data. Here, we report preclinical and clinical results from treatment of sarcoma with oncolytic adenovirus Ad5/3-D24-GMCSF (CGTG-102). Ad5/3-D24-GMCSF is a serotype chimeric oncolytic adenovirus coding for human granulocyte-macrophage colony-stimulating factor (GM-CSF). The efficacy of Ad5/3-D24-GMCSF was evaluated on a panel of soft-tissue sarcoma (STS) cell lines and in two animal models. Sarcoma specific human data were also collected from the Advanced Therapy Access Program (ATAP), in preparation for further clinical development. Efficacy was seen in both in vitro and in vivo STS models. Fifteen patients with treatment-refractory STS (13/15) or primary bone sarcoma (2/15) were treated in ATAP, and treatments appeared safe and well-tolerated. A total of 12 radiological RECIST response evaluations were performed, and two cases of minor response, six cases of stable disease and four cases of progressive disease were detected in patients progressing prior to virus treatment. Overall, the median survival time post treatment was 170 days. One patient is still alive at 1,459 days post virus treatment. In summary, Ad5/3-D24-GMCSF appears promising for the treatment of advanced STS; a clinical trial for treatment of refractory injectable solid tumors including STS is ongoing.
肉瘤是一种相对罕见的癌症,但在晚期转移性阶段通常无法治愈。溶瘤免疫疗法在过去几年引起了关注,通过瘤内注射已经递送了广泛的溶瘤病毒,具有积极的安全性和有前途的疗效数据。在这里,我们报告了使用溶瘤腺病毒 Ad5/3-D24-GMCSF(CGTG-102)治疗肉瘤的临床前和临床结果。Ad5/3-D24-GMCSF 是一种编码人粒细胞-巨噬细胞集落刺激因子(GM-CSF)的血清型嵌合溶瘤腺病毒。在一系列软组织肉瘤(STS)细胞系和两种动物模型中评估了 Ad5/3-D24-GMCSF 的疗效。为进一步的临床开发,还从高级治疗准入计划(ATAP)中收集了肉瘤特异性的人类数据。在体外和体内 STS 模型中均观察到疗效。在 ATAP 中治疗了 15 名治疗抵抗的 STS(13/15)或原发性骨肉瘤(2/15)患者,治疗似乎安全且耐受良好。共进行了 12 次基于 RECIST 的反应评估,在病毒治疗前进展的患者中,有 2 例轻度反应、6 例稳定疾病和 4 例进展疾病。总体而言,治疗后中位生存时间为 170 天。一名患者在病毒治疗后 1459 天仍存活。总之,Ad5/3-D24-GMCSF 似乎是治疗晚期 STS 的有前途的方法;一项治疗难治性可注射实体瘤(包括 STS)的临床试验正在进行中。