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用于肝细胞癌个体化治疗的肿瘤分子剖析:病例研究

Tumor Molecular Profiling for an Individualized Approach to the Treatment of Hepatocellular Carcinoma: A Patient Case Study.

作者信息

Posadas Kristine, Ankola Anita, Yang Zhaohai, Yee Nelson S

机构信息

Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.

Department of Radiology, Penn State Health Milton S. Hershey Medical Center, Hershey, PA 17033, USA.

出版信息

Biomedicines. 2018 Apr 17;6(2):46. doi: 10.3390/biomedicines6020046.

Abstract

Hepatocellular carcinoma (HCC) is increasing in incidence, and the associated mortality rate remains among the highest. For advanced HCC, sorafenib has been shown to slightly prolong survival, and regorafenib and nivolumab, both recently approved by the United States Food and Drug Administration (FDA), may produce clinical benefits to a limited extent. Systemic chemotherapy has been shown to produce a modest response, but there is no clinically valid biomarker that can be used to predict which patients may benefit. In this case study, we present two patients with metastatic HCC, they received systemic treatment using capecitabine, oxaliplatin, and either bevacizumab or sorafenib. The tumor response to treatment was determined by the progression-free survival (PFS). Molecular profiling of the tumors showed differential expression of biochemical markers and different mutational status of the and β-catenin () genes. We hypothesize that the PFS correlates with the tumor molecular profiles, which may be predictive of the therapeutic response to systemic chemotherapy. Further investigation is indicated to correlate tumor biomarkers and treatment responses, with the objective of personalizing the therapies for patients with advanced HCC.

摘要

肝细胞癌(HCC)的发病率正在上升,其相关死亡率仍位居前列。对于晚期HCC,索拉非尼已被证明可略微延长生存期,而最近美国食品药品监督管理局(FDA)批准的瑞戈非尼和纳武单抗可能在一定程度上产生临床益处。全身化疗已显示出适度的反应,但尚无临床上有效的生物标志物可用于预测哪些患者可能受益。在本病例研究中,我们展示了两名转移性HCC患者,他们接受了使用卡培他滨、奥沙利铂以及贝伐单抗或索拉非尼的全身治疗。通过无进展生存期(PFS)来确定肿瘤对治疗的反应。肿瘤的分子分析显示生化标志物的差异表达以及β-连环蛋白(β-catenin)基因的不同突变状态。我们假设PFS与肿瘤分子谱相关,这可能预测对全身化疗的治疗反应。需要进一步研究以关联肿瘤生物标志物和治疗反应,目的是为晚期HCC患者实现个性化治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c70a/6027424/c3a4c8c6513f/biomedicines-06-00046-g001.jpg

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