Intratumor genetic heterogeneity in squamous cell carcinoma of the oral cavity

被引:21
作者
Zandberg, Dan P. [1 ]
Tallon, Luke J. [2 ]
Nagaraj, Sushma [2 ]
Sadzewicz, Lisa K. [2 ]
Zhang, Yuji [3 ]
Strome, Maxwell B. [4 ]
Zhao, Xuechu E. [2 ]
Vavikolanu, Kranthi [2 ]
Zhang, Xiaoyu [5 ]
Papadimitriou, John C. [6 ]
Hubbard, Fleesie A. [5 ]
Bentzen, Soren M. [3 ]
Strome, Scott E. [5 ]
Fraser, Claire M. [2 ]
机构
[1] UPMC Hillman Canc Ctr, Dept Hematol Oncol, 5150 Ctr Ave,5th Floor, Pittsburgh, PA 15232 USA
[2] Univ Maryland, Sch Med, Dept Med, Inst Genome Sci, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Dept Epidemiol & Publ Hlth, Baltimore, MD 21201 USA
[4] Univ Michigan, Coll Literature Sci & Arts, Ann Arbor, MI 48109 USA
[5] Univ Maryland, Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Baltimore, MD 21201 USA
[6] Univ Maryland, Sch Med, Dept Pathol, Baltimore, MD 21201 USA
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2019年 / 41卷 / 08期
关键词
genetic; heterogeneity; SCCHN; oral cavity; squamous cell carcinoma; MUTATIONAL LANDSCAPE; GENOMIC INSTABILITY; TUMOR EVOLUTION; PD-1; BLOCKADE; COPY NUMBER; CANCER; HEAD; SENSITIVITY; DISCOVERY; MODEL;
D O I
10.1002/hed.25719
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background We sought to evaluate intratumor heterogeneity in squamous cell carcinoma of the oral cavity (OCC) and specifically determine the effect of physical separation and histologic differentiation within the same tumor. Methods We performed whole exome sequencing on five biopsy sites-two from well-differentiated, two from poorly differentiated regions, and one from normal parenchyma-from five primary OCC specimens. Results We found high levels of intratumor heterogeneity and, in four primary tumors, identified only 0 to 2 identical mutations in all subsites. We found that the heterogeneity inversely correlated with physical separation and that pairs of well-differentiated samples were more similar to each other than analogous poorly differentiated specimens. Only TP53 mutations, but not other purported "driver mutations" in head and neck squamous cell carcinoma, were found in multiple biopsy sites. Conclusion These data highlight the challenges to characterization of the mutational landscape of OCC with single site biopsy and have implications for personalized medicine.
引用
收藏
页码:2514 / 2524
页数:11
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