Danielli Riccardo, Patuzzo Roberto, Di Giacomo Anna Maria, Gallino Gianfranco, Maurichi Andrea, Di Florio Annabella, Cutaia Ornella, Lazzeri Andrea, Fazio Carolina, Miracco Clelia, Giovannoni Leonardo, Elia Giuliano, Neri Dario, Maio Michele, Santinami Mario
Medical Oncology and Immunotherapy, Department of Oncology, University Hospital of Siena, Siena, Italy.
Cancer Immunol Immunother. 2015 Aug;64(8):999-1009. doi: 10.1007/s00262-015-1704-6. Epub 2015 May 14.
The intratumoral injection of cytokines, in particular IL2, has shown promise for cutaneous melanoma patients with unresectable disease or continuous recurrence despite surgery. We recently reported that the intralesional injection of L19-IL2, an immunocytokine combining IL2 and the human monoclonal antibody fragment L19, resulted in efficient regional control of disease progression, increased time to distant metastasis and evidence of effect on circulating immune cell populations. We have also shown in preclinical models of cancer a remarkable synergistic effect of the combination of L19-IL2 with L19-TNF, a second clinical-stage immunocytokine, based on the same L19 antibody fused to TNF. Here, we describe the results of a phase II clinical trial based on the intralesional administration of L19-IL2 and L19-TNF in patients with stage IIIC and IVM1a metastatic melanoma, who were not candidate to surgery. In 20 efficacy-evaluable patients, 32 melanoma lesions exhibited complete responses upon intralesional administration of the two products, with mild side effects mainly limited to injection site reactions. Importantly, we observed complete responses in 7/13 (53.8 %) non-injected lesions (4 cutaneous, 3 lymph nodes), indicating a systemic activity of the intralesional immunostimulatory treatment. The intralesional administration of L19-IL2 and L19-TNF represents a simple and effective method for the local control of inoperable melanoma lesions, with a potential to eradicate them or make them suitable for a facile surgical removal of the residual mass.
瘤内注射细胞因子,特别是白细胞介素-2(IL2),已显示出对无法切除或术后持续复发的皮肤黑色素瘤患者具有前景。我们最近报道,瘤内注射L19-IL2(一种将IL2与人单克隆抗体片段L19结合的免疫细胞因子)可有效局部控制疾病进展,延长远处转移时间,并对循环免疫细胞群体产生影响。我们还在癌症临床前模型中表明,基于与肿瘤坏死因子(TNF)融合的相同L19抗体的第二种临床阶段免疫细胞因子L19-TNF与L19-IL2联合使用具有显著的协同效应。在此,我们描述了一项II期临床试验的结果,该试验基于对IIIC期和IVM1a期转移性黑色素瘤患者瘤内注射L19-IL2和L19-TNF,这些患者不适合手术。在20例可进行疗效评估的患者中,32个黑色素瘤病灶在瘤内注射这两种产品后出现完全缓解,副作用轻微,主要局限于注射部位反应。重要的是,我们在13个未注射的病灶(4个皮肤病灶、3个淋巴结病灶)中的7个(53.8%)观察到完全缓解,表明瘤内免疫刺激治疗具有全身活性。瘤内注射L19-IL2和L19-TNF是一种简单有效的方法,可局部控制无法手术切除的黑色素瘤病灶,有可能根除这些病灶或使其适合轻松手术切除残留肿块。