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首页> 外文期刊>Case Reports in Oncology >Integrated Diagnostic Model That Incorporates Epstein-Barr Virus DNA, Imaging, and Nasal Endoscopy to Stratify Primary Tumor and Lymph Nodes in a Patient with N1 Nasopharyngeal Carcinoma: Multidisciplinary Management
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Integrated Diagnostic Model That Incorporates Epstein-Barr Virus DNA, Imaging, and Nasal Endoscopy to Stratify Primary Tumor and Lymph Nodes in a Patient with N1 Nasopharyngeal Carcinoma: Multidisciplinary Management

机译:整合了爱泼斯坦-巴尔病毒DNA,成像和鼻内窥镜检查以对N1鼻咽癌患者的原发肿瘤和淋巴结进行分层的综合诊断模型:多学科管理

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摘要

Nasopharyngeal carcinoma (NPC) is an epithelial malignancy, with a high metastatic potential. Epstein-Barr virus (EBV) infection plays a fundamental role, even if it is not well understood. The diagnosis of the disease in its early stage is infrequent. Imaging studies, positron emission tomography scans in addition to clinical examination, endoscopic examination, and biopsy provide information on the extent of the disease. The application of neoadjuvant chemotherapy followed by concomitant chemoradiation can improve the control of NPC. In March 2016, a 54-year-old male with NPC cT1 cN2 cM0, stage III (8th edition of American Joint Committee on Cancer (AJCC) staging system) underwent to a two-step treatment: induction chemotherapy by TPF regimen (docetaxel, cisplatin, 5-fluorouracil), followed by concomitant chemoradiotherapy (weekly cisplatin). The quantity of free plasma EBV-DNA can be related to the disease stage, and the detection of EBV-DNA during follow-up can be predictive of distant metastases. Especially, either plasma or serum EBV-DNA titer is estimated to reflect tumor volume. Biologically, such EBV-DNA reflects reproduced or released DNA from dead or dying tumor cells. On the other hand, EBV-specific DNA released as exosome may reflect the biological feature of the alive NPC tumor cell. The follow-up is ongoing after 21 months from a complete response.
机译:鼻咽癌(NPC)是一种上皮恶性肿瘤,具有很高的转移潜力。爱泼斯坦-巴尔病毒(EBV)感染起着根本作用,即使尚不为人所知。该病早期诊断很少。除了临床检查,内窥镜检查和活检之外,影像学研究,正电子发射断层扫描也提供了有关疾病范围的信息。新辅助化疗后再进行化学放疗可以改善对NPC的控制。 2016年3月,一名54岁,三期NPC cT1 cN2 cM0​​的男性(美国癌症联合委员会(AJCC)分期系统第8版)接受了两步治疗:TPF方案(多西他赛,顺铂,5-氟尿嘧啶),然后进行放化疗(每周一次顺铂)。游离血浆EBV-DNA的数量可能与疾病阶段有关,并且在随访期间检测EBV-DNA可以预测远处转移。特别地,估计血浆或血清EBV-DNA滴度可反映肿瘤体积。从生物学上讲,这种EBV-DNA反映了已死亡或垂死的肿瘤细胞中复制或释放的DNA。另一方面,作为外来体释放的EBV特异性DNA可能反映了存活的NPC肿瘤细胞的生物学特征。全面回应后的21个月,正在进行随访。

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