Department of Medical Oncology, Center for Immuno-Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Department of Data Science, Dana-Farber Cancer Institute, Boston, MA, USA.
Cancer Immunol Immunother. 2024 Jan 18;73(1):17. doi: 10.1007/s00262-023-03593-2.
Vascular endothelial growth factor is associated with reduced immune response and impaired anti-tumor activity. Combining antiangiogenic agents with immune checkpoint inhibition can overcome this immune suppression and enhance treatment efficacy.
This study investigated the combination of ziv-aflibercept anti-angiogenic therapy with pembrolizumab in patients with advanced melanoma resistant to anti-PD-1 treatment. Baseline and on-treatment plasma and PBMC samples were analyzed by multiplex protein assay and mass cytometry, respectively.
In this Phase 1B study (NCT02298959), ten patients with advanced PD-1-resistant melanoma were treated with a combination of ziv-aflibercept (at 2-4 mg/kg) plus pembrolizumab (at 2 mg/kg), administered intravenously every 2 weeks. Two patients (20%) achieved a partial response, and two patients (20%) experienced stable disease (SD) as the best response. The two responders had mucosal melanoma, while both patients with SD had ocular melanoma. The combination therapy demonstrated clinical activity and acceptable safety, despite the occurrence of adverse events. Changes in plasma analytes such as platelet-derived growth factor and PD-L1 were explored, indicating potential alterations in myeloid cell function. Higher levels of circulating CXCL10 in non-responding patients may reflect pro-tumor activity. Specific subsets of γδ T cells were associated with poor clinical outcomes, suggesting impaired γδ T-cell function in non-responding patients.
Although limited by sample size and follow-up, these findings highlight the potential of the combination of ziv-aflibercept antiangiogenic therapy with pembrolizumab in patients with advanced melanoma resistant to anti-PD-1 treatment and the need for further research to improve outcomes in anti-PD-1-resistant melanoma.
NCT02298959.
血管内皮生长因子与免疫反应减弱和抗肿瘤活性受损有关。将抗血管生成药物与免疫检查点抑制相结合可以克服这种免疫抑制,增强治疗效果。
本研究调查了在对 PD-1 治疗耐药的晚期黑色素瘤患者中,联合使用 ziv-aflibercept 抗血管生成治疗和 pembrolizumab 的效果。通过多重蛋白检测和质谱细胞术分别分析了基线和治疗期间的血浆和 PBMC 样本。
在这项 1b 期研究(NCT02298959)中,10 名对 PD-1 耐药的晚期黑色素瘤患者接受了 ziv-aflibercept(2-4 mg/kg)联合 pembrolizumab(2 mg/kg)治疗,每 2 周静脉输注一次。两名患者(20%)获得部分缓解,两名患者(20%)最佳反应为疾病稳定(SD)。两名应答者患有黏膜黑色素瘤,而两名 SD 患者均患有眼黑色素瘤。尽管发生了不良反应,但联合治疗显示出了临床活性和可接受的安全性。还探索了血浆分析物(如血小板衍生生长因子和 PD-L1)的变化,表明髓样细胞功能可能发生改变。非应答者循环 CXCL10 水平较高可能反映了促肿瘤活性。γδ T 细胞的特定亚群与不良临床结局相关,提示非应答者的 γδ T 细胞功能受损。
尽管受到样本量和随访的限制,但这些发现强调了 ziv-aflibercept 抗血管生成治疗联合 pembrolizumab 在对 PD-1 治疗耐药的晚期黑色素瘤患者中的应用潜力,需要进一步研究以改善对 PD-1 耐药的黑色素瘤患者的结局。
NCT02298959。