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一种新型的双元基因标志物,用于在临床中风险且接受术后放疗的头颈部鳞状细胞癌患者中识别高危患者。

A Novel 2-Metagene Signature to Identify High-Risk HNSCC Patients amongst Those Who Are Clinically at Intermediate Risk and Are Treated with PORT.

作者信息

Patil Shivaprasad, Linge Annett, Hiepe Hannah, Grosser Marianne, Lohaus Fabian, Gudziol Volker, Kemper Max, Nowak Alexander, Haim Dominik, Tinhofer Inge, Budach Volker, Guberina Maja, Stuschke Martin, Balermpas Panagiotis, Grün Jens von der, Schäfer Henning, Grosu Anca-Ligia, Abdollahi Amir, Debus Jürgen, Ganswindt Ute, Belka Claus, Pigorsch Steffi, Combs Stephanie E, Boeke Simon, Zips Daniel, Jöhrens Korinna, Baretton Gustavo B, Baumann Michael, Krause Mechthild, Löck Steffen

机构信息

German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany and German Cancer Consortium (DKTK), partner site Dresden, 01307 Dresden, Germany.

OncoRay-National Center for Radiation Research in Oncology, Faculty of Medicine and UniversityHospital Carl Gustav Carus, Technische Universität Dresden, Helmholtz-Zentrum Dresden-Rossendorf, 01307 Dresden, Germany.

出版信息

Cancers (Basel). 2022 Jun 20;14(12):3031. doi: 10.3390/cancers14123031.

Abstract

(1) Background: Patients with locally advanced head and neck squamous cell carcinoma (HNSCC) who are biologically at high risk for the development of loco−regional recurrences after postoperative radiotherapy (PORT) but at intermediate risk according to clinical risk factors may benefit from additional concurrent chemotherapy. In this matched-pair study, we aimed to identify a corresponding predictive gene signature. (2) Methods: Gene expression analysis was performed on a multicenter retrospective cohort of 221 patients that were treated with postoperative radiochemotherapy (PORT-C) and 283 patients who were treated with PORT alone. Propensity score analysis was used to identify matched patient pairs from both cohorts. From differential gene expression analysis and Cox regression, a predictive gene signature was identified. (3) Results: 108 matched patient pairs were selected. We identified a 2-metagene signature that stratified patients into risk groups in both cohorts. The comparison of the high-risk patients between the two types of treatment showed higher loco−regional control (LRC) after treatment with PORT-C (p < 0.001), which was confirmed by a significant interaction term in Cox regression (p = 0.027), i.e., the 2-metagene signature was indicative for the type of treatment. (4) Conclusion: We have identified a novel gene signature that may be helpful to identify patients with high-risk HNSCC amongst those at intermediate clinical risk treated with PORT, who may benefit from additional concurrent chemotherapy.

摘要

(1) 背景:局部晚期头颈部鳞状细胞癌(HNSCC)患者在术后放疗(PORT)后发生局部区域复发的生物学风险较高,但根据临床风险因素属于中度风险,可能从额外的同步化疗中获益。在这项配对研究中,我们旨在确定一个相应的预测基因特征。(2) 方法:对221例接受术后放化疗(PORT-C)的患者和283例仅接受PORT的患者组成的多中心回顾性队列进行基因表达分析。倾向评分分析用于从两个队列中确定配对的患者对。通过差异基因表达分析和Cox回归,确定了一个预测基因特征。(3) 结果:选择了108对配对患者。我们确定了一个双元基因特征,可将两个队列中的患者分为风险组。两种治疗方式的高危患者比较显示,PORT-C治疗后的局部区域控制(LRC)更高(p < 0.001),Cox回归中的显著交互项证实了这一点(p = 0.027),即双元基因特征可指示治疗类型。(4) 结论:我们确定了一种新的基因特征,可能有助于在接受PORT治疗的中度临床风险患者中识别高危HNSCC患者,这些患者可能从额外的同步化疗中获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d82/9221048/277aa20f4e09/cancers-14-03031-g001.jpg

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