| Literature DB >> 28196593 |
Alberto Bardelli1, Klaus Pantel2.
Abstract
The inherent molecular heterogeneity of metastatic tumors and the ability of cancer genomes to dynamically evolve are not properly captured by tissue specimens. Analysis of cell-free DNA and circulating tumor cells has the potential to change clinical practice by exploiting blood rather than tissue as a source of information. Liquid biopsies are already used to monitor disease response and track the emergence of drug resistance. The suitability of blood-based molecular profiles for early detection and monitoring minimal residual disease is being evaluated. In this review, we address open questions in this fast-evolving field of research.Entities:
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Year: 2017 PMID: 28196593 DOI: 10.1016/j.ccell.2017.01.002
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743