A data- and model-driven approach for cancer treatment. German version

被引:0
|
作者
Schade, Sophia [1 ]
Ogilvie, Lesley A. [1 ]
Kessler, Thomas [1 ]
Schuette, Moritz [1 ]
Wierling, Christoph [1 ]
Lange, Bodo M. [1 ]
Lehrach, Hans [1 ,2 ]
Yaspo, Marie-Laure [1 ,2 ]
机构
[1] Alacris Theranost GmbH, Max Planck Str 3, D-12489 Berlin, Germany
[2] Max Planck Inst Mol Genet, Berlin, Germany
来源
ONKOLOGE | 2019年 / 25卷
关键词
Precision medicine; Biomarkers; tumor; Gene expression profiling; Translational medical research; Molecular targeted therapy; THERAPY; LANDSCAPE; BLOCKADE;
D O I
10.1007/s00761-019-00652-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We are unique and so are our diseases. Our genomes, disease histories, behavior, and lifestyles are all different. It is not too surprising, therefore, that we often respond differently to the drugs we receive. Cancer, in particular, is a complex and heterogeneous disease, originating in patients with different genomes, in cells with different epigenomes, formed and evolving on the basis of random processes, with the response to therapy not only depending on the individual cancer cell but also on many features of the patient. Selection of an optimal therapy will therefore require a deep molecular analysis comprising both the patient and their tumor (e.g., comprehensive molecular tumor analysis [CMTA]), and much better personalized prediction of response to possible therapies. Currently, we are at an inflection point in which advances in technology, decreases in the costs of sequencing and other molecular analyses, and increases in computing power are converging, forming the foundation to build a data-driven approach to personalized oncology. Here, we discuss the deep molecular characterization of individual tumors and patients as the basis of not only current precision oncology but also of computational models ('digital twins'), forming the foundation of a truly personalized therapy selection of the future.
引用
收藏
页码:109 / 115
页数:7
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