根据靶向测序,成纤维细胞生长因子家族畸变可能是流行病学上低风险患者头颈部鳞状细胞癌的驱动因素

Brittny N. Tillman, M. Yanik, A. Birkeland, C. Liu, D. Hovelson, A. Cani, N. Palanisamy, Shannon Carskadon, T. Carey, C. Bradford, S. Tomlins, J. Mchugh, M. Spector, J. Brenner
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引用次数: 27

摘要

流行病学低风险(ELR)头颈部鳞状细胞癌(HNSCC)患者的靶向测序可以帮助识别新的驱动因素或丢失的抑制因子,从而实现精准医疗方案和提高生存率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fibroblast growth factor family aberrations as a putative driver of head and neck squamous cell carcinoma in an epidemiologically low‐risk patient as defined by targeted sequencing
Targeted sequencing of patients with epidemiologically low‐risk (ELR) head and neck squamous cell carcinoma (HNSCC) could help identify novel drivers or lost suppressors leading to precision medicine protocols and improved survival rates.
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