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A retrospective analysis of the clinicopathological and molecular characteristics of pulmonary blastoma

机译:肺母细胞瘤临床病理和分子特征的回顾性分析

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Purpose: The aim of this study was to analyze and summarize the clinicopathological and molecular characteristics of classic biphasic pulmonary blastoma (PB) to improve its diagnosis and treatment. Patients and methods: A retrospective analysis was performed in patients who were diagnosed with PB at Sun Yat-Sen University Cancer Center from March 1995 to March 2015. Genomic DNA was profiled using a capture-based targeted sequencing panel. Results: Sixteen patients with an average age of 40 years were included in this study. Accurate preoperative diagnosis was very challenging as surgically resected tissues with immunohistochemical staining were required for the diagnosis. Surgery was the optimal treatment for localized disease and there was no standard management for metastatic disease. Mutations were detected among 9 out of the 56 genes profiled, including BRCA2 , ERBB4 , ALK , MET , BRAF , RAF1 , PTEN , EGFR , and PIK3CA . Conclusion: Due to the low incidence rate and the reclassification of PB, no standard treatment is available. Although the numbers of cases are few with varying individual experiences, it is important to improve our understanding regarding this rare lung cancer. Targeted DNA sequencing may be of clinical use for molecular testing and the effects of targeted therapy need to be confirmed.
机译:目的:本研究旨在分析和总结经典双相性肺母细胞瘤(PB)的临床病理和分子特征,以改善其诊断和治疗。患者和方法:回顾性分析从1995年3月至2015年3月在中山大学癌症中心诊断为PB的患者。使用基于捕获的靶向测序小组对基因组DNA进行了分析。结果:16位平均年龄为40岁的患者被纳入本研究。准确的术前诊断非常具有挑战性,因为诊断需要手术切除的组织进行免疫组织化学染色。手术是局部疾病的最佳治疗方法,对转移性疾病没有标准的治疗方法。在56个基因中的9个基因中检测到突变,包括BRCA2,ERBB4,ALK,MET,BRAF,RAF1,PTEN,EGFR和PIK3CA。结论:由于PB的低发生率和重分类,目前尚无标准治疗方法。尽管案例的数量很少,而且个人经历各不相同,但重要的是增进我们对这种罕见肺癌的了解。靶向DNA测序可能在临床上用于分子检测,需要确认靶向治疗的效果。

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