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西妥昔单抗单药治疗转移性口咽鳞状细胞癌患者的显著疗效:分子层面的见解

Exceptional response to cetuximab monotherapy in a patient with metastatic oropharyngeal squamous cell carcinoma: a molecular insight.

作者信息

Peddi Prakash, Paryani Bhavna, Takalkar Amol, Bundrick Paige, Ponugupati John, Nair Binu, El-Osta Hazem

机构信息

Department of Medicine, Division of Hematology-Oncology, Louisiana State University Health Sciences Center, Shreveport, LA, USA.

Department of Radiology, Louisiana State University Health Sciences Center, Shreveport, LA, USA.

出版信息

Onco Targets Ther. 2016 Feb 9;9:705-9. doi: 10.2147/OTT.S99667. eCollection 2016.

Abstract

BACKGROUND

Metastatic head and neck squamous cell carcinoma (HNSCC) carries a very poor prognosis. A better understanding of the molecular driver of the disease and the identification of biomarkers of response remain paramount for an effective personalized therapy.

CASE REPORT

We report an original case of a 56-year-old patient diagnosed with metastatic HNSCC to both kidneys, who experienced a long-lasting complete response to a single-agent cetuximab, a monoclonal antibody-targeting EGFR. Comprehensive multiplatform biomarker analysis of the tumor revealed the presence of phosphatidyl-inositol 3 kinase mutation, EGFR overexpression, and the absence of PD-1/PD-L1 expression. Since PI3K, a downstream effector of EGFR, is activated, the tumor regression may have occurred mainly through a cetuximab-induced immune-mediated response, rather than EGFR signal blockade. It is plausible that this effect was enhanced by the lack of PD-1 and PD-L1 expression.

CONCLUSION

Our case proposes that the absence of PD-1 and PD-L1 expression in conjunction with EGFR overexpression may correlate with better response to cetuximab in HNSCC. This hypothesis needs to be examined through a large clinical trial.

摘要

背景

转移性头颈部鳞状细胞癌(HNSCC)的预后非常差。更好地了解该疾病的分子驱动因素并识别反应生物标志物对于有效的个性化治疗仍然至关重要。

病例报告

我们报告了一例56岁的患者,诊断为双侧肾脏转移性HNSCC,该患者对单药西妥昔单抗(一种靶向表皮生长因子受体(EGFR)的单克隆抗体)产生了持久的完全缓解。对肿瘤进行的综合多平台生物标志物分析显示存在磷脂酰肌醇3激酶突变、EGFR过表达,且不存在程序性死亡受体1(PD-1)/程序性死亡配体1(PD-L1)表达。由于EGFR的下游效应器磷脂酰肌醇3激酶被激活,肿瘤消退可能主要是通过西妥昔单抗诱导的免疫介导反应发生的,而不是通过EGFR信号阻断。PD-1和PD-L1表达的缺失可能增强了这种效应,这似乎是合理的。

结论

我们的病例表明,在HNSCC中,PD-1和PD-L1表达的缺失与EGFR过表达相结合可能与对西妥昔单抗的更好反应相关。这一假设需要通过大型临床试验进行检验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10cd/4755421/5d191ebecaeb/ott-9-705Fig1.jpg

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