Adam Julien, Tomasic Gorana, Robert Caroline
Département de biologie et pathologie médicales, Gustave-Roussy, 114, rue Edouard-Vaillant, 94805 Villejuif, France; Inserm U981, Gustave Roussy, 94805 Villejuif, France.
Département de biologie et pathologie médicales, Gustave-Roussy, 114, rue Edouard-Vaillant, 94805 Villejuif, France.
Ann Pathol. 2017 Feb;37(1):55-60. doi: 10.1016/j.annpat.2016.12.011. Epub 2017 Jan 19.
Prognosis and treatment of advanced melanoma have been transformed by the success of immunotherapies, in particular agents targeting PD-1. PD-L1 expression assessed by immunohistochemistry in not an effective predictive biomarker to select patients in this tumor type, since significant clinical benefit was observed in the group of patients with negative tumors. The predictive value of PD-L1 testing to select patients for combination of anti-PD-1 and anti-CTLA-4 agents is under evaluation. Other tissue biomarkers are emerging to identify sensitive tumors to anti-PD-1 agents. In particular, assessment of immune infiltrates in tumor tissue, mutational load and tumor neoantigens seem promising in melanoma.
免疫疗法的成功,尤其是针对PD-1的药物,改变了晚期黑色素瘤的预后和治疗方式。通过免疫组织化学评估的PD-L1表达并不是选择该肿瘤类型患者的有效预测生物标志物,因为在肿瘤为阴性的患者组中也观察到了显著的临床获益。PD-L1检测对于选择接受抗PD-1和抗CTLA-4联合治疗患者的预测价值正在评估中。其他组织生物标志物正在出现,以识别对抗PD-1药物敏感的肿瘤。特别是,肿瘤组织中的免疫浸润、突变负荷和肿瘤新抗原评估在黑色素瘤中似乎很有前景。