γδ T 细胞调节小细胞肺癌中的抗肿瘤免疫
γδ T cells modulate anti-tumor immunity in small cell lung cancer.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Ziv-aflibercept plus pembrolizumab in patients with advanced melanoma resistant to anti-PD-1 treatment.
Ziv-aflibercept plus pembrolizumab in patients with advanced melanoma resistant to anti-PD-1 treatment.
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血管内皮生长因子与免疫应答降低和抗肿瘤活性受损相关。将抗血管生成药物与免疫检查点抑制联合使用可以克服这种免疫抑制并提高治疗效果。
本研究探讨了ziv-aflibercept抗血管生成治疗联合pembrolizumab在抗PD-1治疗耐药的晚期黑色素瘤患者中的应用。分别通过多重蛋白检测和质谱流式细胞术对基线和治疗期间的血浆和PBMC样本进行分析。
在这项1B期研究(NCT02298959)中,十名晚期PD-1耐药黑色素瘤患者接受了ziv-aflibercept(2-4 mg/kg)联合pembrolizumab(2 mg/kg)的治疗,每2周静脉给药一次。两名患者(20%)达到部分缓解,两名患者(20%)的最佳缓解为疾病稳定(SD)。两名缓解者患有黏膜黑色素瘤,而两名SD患者均患有眼部黑色素瘤。尽管出现了不良事件,该联合治疗仍显示出临床活性和可接受的安全性。研究探索了血浆分析物如血小板衍生生长因子和PD-L1的变化,提示髓系细胞功能可能发生改变。非缓解患者中循环CXCL10水平较高可能反映促肿瘤活性。特定的γδ T细胞亚群与不良临床结局相关,提示非缓解患者中γδ T细胞功能受损。
尽管受样本量和随访时间限制,这些发现凸显了ziv-aflibercept抗血管生成治疗联合pembrolizumab在抗PD-1治疗耐药的晚期黑色素瘤患者中的潜力,以及需要进一步研究以改善抗PD-1耐药黑色素瘤的结局。
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. TRIAL REGISTRATION NUMBER: NCT02298959.
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