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默克尔细胞癌中免疫检查点抑制剂反应生物标志物的最新综述:默克尔细胞癌与免疫疗法

An Updated Review of the Biomarkers of Response to Immune Checkpoint Inhibitors in Merkel Cell Carcinoma: Merkel Cell Carcinoma and Immunotherapy.

作者信息

Fojnica Adnan, Ljuca Kenana, Akhtar Saghir, Gatalica Zoran, Vranic Semir

机构信息

Institute of Virology, TUM School of Medicine, Technical University of Munich, 81675 Munich, Germany.

Molecular Biology and Biochemistry, Gottfried Schatz Research Center, Medical University of Graz, 8036 Graz, Austria.

出版信息

Cancers (Basel). 2023 Oct 20;15(20):5084. doi: 10.3390/cancers15205084.

Abstract

Merkel cell carcinoma (MCC) is primarily a disease of the elderly Caucasian, with most cases occurring in individuals over 50. Immune checkpoint inhibitors (ICI) treatment has shown promising results in MCC patients. Although ~34% of MCC patients are expected to exhibit at least one of the predictive biomarkers (PD-L1, high tumor mutational burden/TMB-H/, and microsatellite instability), their clinical significance in MCC is not fully understood. PD-L1 expression has been variably described in MCC, but its predictive value has not been established yet. Our literature survey indicates conflicting results regarding the predictive value of TMB in ICI therapy for MCC. Avelumab therapy has shown promising results in Merkel cell polyomavirus (MCPyV)-negative MCC patients with TMB-H, while pembrolizumab therapy has shown better response in patients with low TMB. A study evaluating neoadjuvant nivolumab therapy found no significant difference in treatment response between the tumor etiologies and TMB levels. In addition to ICI therapy, other treatments that induce apoptosis, such as milademetan, have demonstrated positive responses in MCPyV-positive MCC, with few somatic mutations and wild-type . This review summarizes current knowledge and discusses emerging and potentially predictive biomarkers for MCC therapy with ICI.

摘要

默克尔细胞癌(MCC)主要是一种老年白种人的疾病,大多数病例发生在50岁以上的个体中。免疫检查点抑制剂(ICI)治疗已在MCC患者中显示出有前景的结果。尽管预计约34%的MCC患者会表现出至少一种预测性生物标志物(程序性死亡受体配体1/PD-L1/、高肿瘤突变负荷/TMB-H/和微卫星不稳定性),但其在MCC中的临床意义尚未完全明确。PD-L1表达在MCC中的描述各不相同,但其预测价值尚未确立。我们的文献调查表明,关于TMB在ICI治疗MCC中的预测价值存在相互矛盾的结果。阿维鲁单抗治疗在TMB-H的默克尔细胞多瘤病毒(MCPyV)阴性MCC患者中显示出有前景的结果,而帕博利珠单抗治疗在TMB低的患者中显示出更好的反应。一项评估新辅助纳武利尤单抗治疗的研究发现,肿瘤病因和TMB水平之间的治疗反应没有显著差异。除了ICI治疗外,其他诱导细胞凋亡的治疗方法,如米拉地坦,已在MCPyV阳性MCC中显示出阳性反应,其体细胞突变很少且为野生型。本综述总结了当前的知识,并讨论了ICI治疗MCC的新兴和潜在预测性生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff66/10605355/dceef61867a4/cancers-15-05084-g001.jpg

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