Liquid Biopsy: From Discovery to Clinical Application

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Liquid Biopsy: From Discovery to Clinical Application. / Alix-Panabières, Catherine; Pantel, Klaus.

In: CANCER DISCOV, Vol. 11, No. 4, 04.2021, p. 858-873.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

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@article{27ec1be464a8442d9c11808e9446983e,
title = "Liquid Biopsy: From Discovery to Clinical Application",
abstract = "Over the past 10 years, circulating tumor cells (CTC) and circulating tumor DNA (ctDNA) have received enormous attention as new biomarkers and subjects of translational research. Although both biomarkers are already used in numerous clinical trials, their clinical utility is still under investigation with promising first results. Clinical applications include early cancer detection, improved cancer staging, early detection of relapse, real-time monitoring of therapeutic efficacy, and detection of therapeutic targets and resistance mechanisms. Here, we propose a conceptual framework of CTC and ctDNA assays and point out current challenges of CTC and ctDNA research, which might structure this dynamic field of translational cancer research. SIGNIFICANCE: The analysis of blood for CTCs or cell-free nucleic acids called {"}liquid biopsy{"} has opened new avenues for cancer diagnostics, including early detection of tumors, improved risk assessment and staging, as well as early detection of relapse and monitoring of tumor evolution in the context of cancer therapies.",
author = "Catherine Alix-Panabi{\`e}res and Klaus Pantel",
note = "{\textcopyright}2021 American Association for Cancer Research.",
year = "2021",
month = apr,
doi = "10.1158/2159-8290.CD-20-1311",
language = "English",
volume = "11",
pages = "858--873",
journal = "CANCER DISCOV",
issn = "2159-8274",
publisher = "American Association for Cancer Research Inc.",
number = "4",

}

RIS

TY - JOUR

T1 - Liquid Biopsy: From Discovery to Clinical Application

AU - Alix-Panabières, Catherine

AU - Pantel, Klaus

N1 - ©2021 American Association for Cancer Research.

PY - 2021/4

Y1 - 2021/4

N2 - Over the past 10 years, circulating tumor cells (CTC) and circulating tumor DNA (ctDNA) have received enormous attention as new biomarkers and subjects of translational research. Although both biomarkers are already used in numerous clinical trials, their clinical utility is still under investigation with promising first results. Clinical applications include early cancer detection, improved cancer staging, early detection of relapse, real-time monitoring of therapeutic efficacy, and detection of therapeutic targets and resistance mechanisms. Here, we propose a conceptual framework of CTC and ctDNA assays and point out current challenges of CTC and ctDNA research, which might structure this dynamic field of translational cancer research. SIGNIFICANCE: The analysis of blood for CTCs or cell-free nucleic acids called "liquid biopsy" has opened new avenues for cancer diagnostics, including early detection of tumors, improved risk assessment and staging, as well as early detection of relapse and monitoring of tumor evolution in the context of cancer therapies.

AB - Over the past 10 years, circulating tumor cells (CTC) and circulating tumor DNA (ctDNA) have received enormous attention as new biomarkers and subjects of translational research. Although both biomarkers are already used in numerous clinical trials, their clinical utility is still under investigation with promising first results. Clinical applications include early cancer detection, improved cancer staging, early detection of relapse, real-time monitoring of therapeutic efficacy, and detection of therapeutic targets and resistance mechanisms. Here, we propose a conceptual framework of CTC and ctDNA assays and point out current challenges of CTC and ctDNA research, which might structure this dynamic field of translational cancer research. SIGNIFICANCE: The analysis of blood for CTCs or cell-free nucleic acids called "liquid biopsy" has opened new avenues for cancer diagnostics, including early detection of tumors, improved risk assessment and staging, as well as early detection of relapse and monitoring of tumor evolution in the context of cancer therapies.

U2 - 10.1158/2159-8290.CD-20-1311

DO - 10.1158/2159-8290.CD-20-1311

M3 - SCORING: Review article

C2 - 33811121

VL - 11

SP - 858

EP - 873

JO - CANCER DISCOV

JF - CANCER DISCOV

SN - 2159-8274

IS - 4

ER -