Cancer Gene Therapy Group, Department of Pathology and Transplantation Laboratory and Haartman Institute, University of Helsinki, Finland.
Oncolytic Adenovirus Group, German Cancer Research Center (Deutsches Krebsforschungszentrum [DKFZ]), Heidelberg, Germany.
Int J Cancer. 2015 Oct 1;137(7):1775-83. doi: 10.1002/ijc.29536. Epub 2015 Apr 11.
Metastatic melanoma is refractory to irradiation and chemotherapy, but amenable to immunological approaches such as immune-checkpoint-inhibiting antibodies or adoptive cell therapies. Oncolytic virus replication is an immunogenic phenomenon, and viruses can be armed with immunostimulatory molecules. Therefore, oncolytic immuno-virotherapy of malignant melanoma is an appealing approach, which was recently validated by a positive phase 3 trial. We investigated the potency of oncolytic adenovirus Ad5/3-D24-GMCSF on a panel of melanoma cell lines and animal models, and summarized the melanoma-specific human data from the Advanced Therapy Access Program (ATAP). The virus effectively eradicated human melanoma cells in vitro and subcutaneous SK-MEL-28 melanoma xenografts in nude mice when combined with low-dose cyclophosphamide. Furthermore, virally-expressed granulocyte-macrophage colony-stimulating factor (GM-CSF) stimulated the differentiation of human monocytes into macrophages. In contrast to human cells, RPMI 1846 hamster melanoma cells exhibited no response to oncolytic viruses and the chimeric 5/3 fiber failed to increase the efficacy of transduction, suggesting limited utility of the hamster model in the context of viruses with this capsid. In ATAP, treatments appeared safe and well-tolerated. Four out of nine melanoma patients treated were evaluable for possible therapy benefit with modified RECIST criteria: one patient had minor response, two had stable disease, and one had progressive disease. Two patients were alive at 559 and 2,149 days after treatment. Ad5/3-D24-GMCSF showed promising efficacy in preclinical studies and possible antitumor activity in melanoma patients refractory to other forms of therapy. This data supports continuing the clinical development of oncolytic adenoviruses for treatment of malignant melanoma.
转移性黑色素瘤对放疗和化疗有抗性,但对免疫疗法如免疫检查点抑制抗体或过继细胞疗法敏感。溶瘤病毒复制是一种免疫原性现象,病毒可以携带免疫刺激分子。因此,溶瘤免疫病毒疗法是治疗恶性黑色素瘤的一种有吸引力的方法,最近一项阳性 3 期试验对此进行了验证。我们研究了溶瘤腺病毒 Ad5/3-D24-GMCSF 在一系列黑色素瘤细胞系和动物模型中的效力,并总结了 Advanced Therapy Access Program(ATAP)中黑色素瘤特异性的人类数据。当与低剂量环磷酰胺联合使用时,该病毒可有效消除体外的人类黑色素瘤细胞和裸鼠皮下 SK-MEL-28 黑色素瘤异种移植物。此外,病毒表达的粒细胞-巨噬细胞集落刺激因子(GM-CSF)可刺激人单核细胞分化为巨噬细胞。与人类细胞不同,RPMI 1846 仓鼠黑色素瘤细胞对溶瘤病毒没有反应,嵌合 5/3 纤维也不能增加转导的疗效,这表明在具有这种衣壳的病毒中,仓鼠模型的应用有限。在 ATAP 中,治疗似乎安全且耐受良好。在根据改良 RECIST 标准可评估疗效的 9 名黑色素瘤患者中,有 4 名可能受益于治疗:1 名患者有轻微反应,2 名患者病情稳定,1 名患者病情进展。2 名患者在治疗后 559 天和 2149 天仍存活。Ad5/3-D24-GMCSF 在临床前研究中显示出有希望的疗效,并在对其他形式治疗有抗性的黑色素瘤患者中显示出可能的抗肿瘤活性。这些数据支持继续开发溶瘤腺病毒用于治疗恶性黑色素瘤。