4.7 Review

Liquid biopsies: Potential and challenges

Journal

INTERNATIONAL JOURNAL OF CANCER
Volume 148, Issue 3, Pages 528-545

Publisher

WILEY
DOI: 10.1002/ijc.33217

Keywords

blood; carcinomas; circulating tumor cells; circulating tumor DNA; liquid biopsy

Categories

Funding

  1. European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant [765492]
  2. European IMI research project CANCER-ID [115749-CANCER-ID]
  3. Deutsche Krebshilfe [70112504]
  4. Deutsche Forschungsgemeinschaft (DFG) [SPP2084]
  5. ERC Advanced Investigator Grant INJURMET [834974]
  6. Projekt DEAL
  7. European Research Council (ERC) [834974] Funding Source: European Research Council (ERC)

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Liquid biopsy (LB) presents broad opportunities in oncology, allowing early detection, risk assessment, and monitoring of cancer therapies with comprehensive and real-time information. Circulating tumor cells (CTCs) and circulating tumor-derived DNA (ctDNA) are key LB markers for breast, prostate, lung, and colorectal cancer. Current implementation of LB in clinical practice is hindered by methodological and biological limitations.
The analysis of tumor cells or tumor cell products obtained from blood or other body fluids (liquid biopsy [LB]) provides a broad range of opportunities in the field of oncology. Clinical application areas include early detection of cancer or tumor recurrence, individual risk assessment and therapy monitoring. LB allows to portray the entire disease as tumor cells or tumor cell products are released from all metastatic or primary tumor sites, providing comprehensive and real-time information on tumor cell evolution, therapeutic targets and mechanisms of resistance to therapy. Here, we focus on the most prominent LB markers, circulating tumor cells (CTCs) and circulating tumor-derived DNA (ctDNA), in the blood of patients with breast, prostate, lung and colorectal cancer, as the four most frequent tumor types in Europe. After a brief introduction of key technologies used to detect CTCs and ctDNA, we discuss recent clinical studies on these biomarkers for early detection and prognostication of cancer as well as prediction and monitoring of cancer therapies. We also point out current methodological and biological limitations that still hamper the implementation of LB into clinical practice.

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