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Published August 2020 | Version v1
Journal article

Comparison of liquid-based to tissue-based biopsy analysis by targeted next generation sequencing in advanced non-small cell lung cancer: a comprehensive systematic review

  • 1. Society of Junior Doctors. Oncology Working Group (Greece)
  • 2. Theageneio Anticancer Hospital. 1st Department of Medical Oncology (Greece)
  • 3. European University of Cyprus. School of Medicine (Cyprus)
  • 4. Athens University of Economics and Business (Greece)
  • 5. Massachusetts General Hospital. Department of Pathology, Harvard Medical School (United States)
  • 6. Seoul National University Hospital. Department of Pathology (Korea, Republic of)
  • 7. Duke University Medical Center. Department of Surgery (United States)

Description

Purpose

: To explore whether targeted next generation sequencing (NGS) of liquid biopsy in advanced non-small cell lung cancer (NSCLC) could potentially overcome the innate problems that arise with standard tissue biopsy, like intratumoral heterogeneity and the inability to obtain adequate samples for analysis.

Methods

: The Scopus, Cochrane Library, and MEDLINE (via PubMed) databases were searched for studies with matched tissue and liquid biopsies from advanced NSCLC patients, analyzed with targeted NGS. The number of mutations detected in tissue biopsy only, liquid biopsy only, or both was assessed and the positive percent agreement (PPA) of the two methods was calculated for every clinically relevant gene.

Results

: A total of 644 unique relevant articles were retrieved and data were extracted from 38 studies fulfilling the inclusion criteria. The sample size was composed of 2000 mutations tested in matched tissue and liquid biopsies derived from 1141 patients. No studies analyzed circulating tumor cells. The calculated PPA rates were 53.6% (45/84) for ALK, 53.9% (14/26) for BRAF, 56.5% (13/23) for ERBB2, 67.8% (428/631) for EGFR, 64.2% (122/190) for KRAS, 58.6% (17/29) for MET, 54.6% (12/22) for RET, and 53.3% (8/15) for ROS1. We additionally recorded data for 65 genes that are not recommended by current guidelines for mutational testing. An extra category containing results of unspecified genes was added, with a PPA rate of 55.7% (122/219).

Conclusion

: Despite many advantages, liquid biopsy might be unable to fully substitute its tissue counterpart in detecting clinically relevant mutations in advanced NSCLC patients. However, it may serve as a helpful tool when making therapeutic decisions. More studies are needed to evaluate its role in everyday clinical practice.

Additional details

Identifiers

Publishing Information

Journal Title
Journal of Cancer Research and Clinical Oncology
Journal Volume
146
Journal Issue
8
Journal Page Range
p. 2051-2066
ISSN
0171-5216
CODEN
JCROD7

INIS

Country of Publication
Germany
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
55072071
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
ANIMAL TISSUES; BIOPSY; COMPARATIVE EVALUATIONS; DECISION MAKING; GENE MUTATIONS; GENES; LIQUIDS; LUNGS; MUTATIONS; NEOPLASMS; PATIENTS; TESTING; TUMOR CELLS
Descriptors DEC
ANIMAL CELLS; BODY; DIAGNOSTIC TECHNIQUES; DISEASES; EVALUATION; FLUIDS; MUTATIONS; ORGANS; RESPIRATORY SYSTEM

Optional Information

Copyright
Copyright (c) 2020 © Springer-Verlag GmbH Germany, part of Springer Nature 2020