Beyond tissue biopsy: a diagnostic framework to address tumor heterogeneity in lung cancer

被引:18
作者
Voigt, Wieland [1 ]
Manegold, Christian [2 ]
Pilz, Lothar [2 ]
Wu, Yi-Long [3 ]
Muellauer, Leonard [4 ]
Pirker, Robert [5 ]
Filipits, Martin [6 ]
Niklinski, Jacek [7 ]
Petruzelka, Lubos [8 ,9 ]
Prosch, Helmut [10 ]
机构
[1] Steinbeis Univ Berlin, Med Innovat & Management, Ernst Augustin St 15, D-12498 Berlin, Germany
[2] Heidelberg Univ, Med Fac Mannheim, Heidelberg, Germany
[3] Guangdong Gen Hosp, Guangdong Lung Canc Inst, Guangzhou, Peoples R China
[4] Med Univ Vienna, Dept Pathol, Vienna, Austria
[5] Med Univ Vienna, Dept Med, Vienna, Austria
[6] Med Univ Vienna, Dept Med 1, Inst Canc Res, Vienna, Austria
[7] Med Univ Bialystok, Dept Clin Mol Biol, Bialystok, Poland
[8] Charles Univ Prague, Fac Med 1, Dept Oncol, Prague, Czech Republic
[9] Gen Univ Hosp Prague, Prague, Czech Republic
[10] Med Univ Vienna, Dept Biomed Imaging & Image Guided Therapy, Vienna, Austria
关键词
functional imaging; liquid biopsy; non-small cell lung cancer; tumor heterogeneity; MUTATION STATUS; INTRATUMOR HETEROGENEITY; TREATMENT RESPONSE; F-18-FDG PET/CT; LIQUID BIOPSIES; CT; EGFR; RADIOMICS; DNA; ADENOCARCINOMA;
D O I
10.1097/CCO.0000000000000598
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review The objective of this review is to discuss the strength and limitations of tissue and liquid biopsy and functional imaging to capture spatial and temporal tumor heterogeneity either alone or as part of a diagnostic framework in non-small cell lung cancer (NSCLC). Recent findings NSCLC displays genetic and phenotypic heterogeneity - a detailed knowledge of which is crucial to personalize treatment. Tissue biopsy often lacks spatial and temporal resolution. Thus, NSCLC needs to be characterized by complementary diagnostic methods to resolve heterogeneity. Liquid biopsy offers detection of tumor biomarkers and for example, the classification and monitoring of EGFR mutations in NSCLC. It allows repeated sampling, and therefore, appears promising to address temporal aspects of tumor heterogeneity. Functional imaging methods and emerging image analytic tools, such as radiomics capture temporal and spatial heterogeneity. Further standardization of radiomics is required to allow introduction into clinical routine. To augment the potential of precision therapy, improved diagnostic characterization of tumors is pivotal. We suggest a comprehensive diagnostic framework combining tissue and liquid biopsy and functional imaging to address the known aspects of spatial and temporal tumor heterogeneity on the example of NSCLC. We envision how this framework might be implemented in clinical practice.
引用
收藏
页码:68 / 77
页数:10
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