Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: Analysis of 1806 cases

被引:58
作者
Gatalica, Zoran [1 ]
Millis, Sherri Z. [1 ]
Vranic, Semir [2 ]
Bender, Ryan [1 ]
Basu, Gargi D. [1 ]
Voss, Andreas [1 ]
Von Hoff, Daniel D. [3 ,4 ]
机构
[1] Caris Life Sci, Phoenix, AZ 85040 USA
[2] Univ Sarajevo, Dept Pathol, Ctr Clin, Sarajevo 71000, Bosnia & Herceg
[3] Translat Genom Res Inst, Phoenix, AZ USA
[4] Virginia G Piper Canc Ctr, Phoenix, AZ USA
关键词
cancer of unknown primary; multiplatform; molecular profiling; mutations; targeted therapy; CARCINOMA; THERAPY; ACTIVATION; EXPRESSION; STRATEGIES; MUTATIONS; ORIGIN; TISSUE; TRIAL;
D O I
10.18632/oncotarget.2574
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Cancer of unknown primary (CUP) accounts for approximately 3% of all malignancies. Despite extensive laboratory and imaging efforts, the primary site usually cannot be unequivocally confirmed, and the treatment for the most part remains empirical. Recently, identification of common cancer pathway alterations in diverse cancer lineages has offered an opportunity to provide targeted therapies for patients with CUP, irrespective of the primary site. Patients and Methods: 1806 cancers of unknown primary were identified among more than 63,000 cases profiled at Caris Life Sciences. Multiplatform profiling of the tumor samples included immunohistochemistry, gene sequencing and in situ hybridization methods in an effort to identify changes in biomarkers that are predictive of drug responses. Results: Biomarkers associated with a potential drug benefit were identified in 96% of cases. Biomarkers identified included those associated with potential benefit in nearly all classes of approved cancer drugs (cytotoxic, hormonal, targeted biological drugs). Additionally, biomarkers associated with a potential lack of benefit were identified in numerous cases, which could further refine the management of patients with CUP. Conclusion: Comprehensive biomarker profiling of CUP may provide additional choices in treatment of patients with these difficult to treat malignancies.
引用
收藏
页码:12440 / 12447
页数:8
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