Evidence map›Paper›PMID 41602544›Full record

ReviewFrontiers in molecular biosciences2025

Liquid biopsy in cancer diagnosis and prognosis: a paradigm shift in precision oncology.

Rayane da Silva Abreu, Danielle Dias Pinto Ferreira, Natassia Silva de Araujo, Samuel Horita, Tatiana Martins Tilli, Wim Degrave, Aline Dos Santos Moreira, Mariana Caldas Waghabi

Abstract readReview
In one paragraph

Review in Frontiers in molecular biosciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Rayane da Silva AbreuLaboratory of Applied Genomics and Bioinovations, IOC, Fiocruz, Rio de Janeiro, Brazil.
Danielle Dias Pinto FerreiraLaboratory of Applied Genomics and Bioinovations, IOC, Fiocruz, Rio de Janeiro, Brazil.
Natassia Silva de AraujoLaboratory of Applied Genomics and Bioinovations, IOC, Fiocruz, Rio de Janeiro, Brazil.
Samuel HoritaIntegrated Center for Translational Oncology Research (CIPOT), Rio de Janeiro, Brazil.
Tatiana Martins TilliIntegrated Center for Translational Oncology Research (CIPOT), Rio de Janeiro, Brazil.
Wim DegraveLaboratory of Applied Genomics and Bioinovations, IOC, Fiocruz, Rio de Janeiro, Brazil.
Aline Dos Santos MoreiraLaboratory of Applied Genomics and Bioinovations, IOC, Fiocruz, Rio de Janeiro, Brazil.
Mariana Caldas WaghabiLaboratory of Applied Genomics and Bioinovations, IOC, Fiocruz, Rio de Janeiro, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liquid biopsy has emerged as a transformative tool in precision oncology, offering a minimally invasive approach for cancer detection, monitoring, and treatment guidance. Unlike traditional tissue biopsies, which are invasive and limited by tumor accessibility and sampling bias, liquid biopsy enables real-time tumor assessment through the analysis of circulating biomarkers in blood and other biofluids. This review provides a comprehensive overview of recent advances in liquid biopsy, with a focus on circulating tumor cells (CTCs), circulating tumor DNA (ctDNA), non-coding RNAs, extracellular vesicles (exosomes), and secreted proteins. These biomarkers offer valuable insights into tumor biology, supporting applications in early diagnosis, prognosis, treatment response monitoring, and minimal residual disease detection across various cancer types. We also discuss state-of-the-art methodologies, including next-generation sequencing, digital PCR, microfluidics, proteomics, and emerging artificial intelligence-based approaches that enhance the sensitivity, specificity, and scalability of liquid biopsy assays. Clinical studies demonstrate the potential of liquid biopsy for tailoring targeted therapies, predicting resistance mechanisms, and identifying tumor recurrence earlier than conventional methods. Furthermore, FDA-approved assays and ongoing phase III and IV clinical trials highlight its growing integration into routine clinical practice. Beyond technical innovations, this review examines the global landscape of liquid biopsy, emphasizing opportunities and challenges for implementation across diverse healthcare settings. Disparities in access, particularly between high-income and low- and middle-income countries, underscore the need for strategies that ensure equitable adoption of liquid biopsy technologies worldwide. In summary, liquid biopsy represents a paradigm shift in oncology, bridging innovations in cancer diagnostics with clinical applications. By enabling dynamic, personalized, and less invasive cancer management, it holds great promise for improving patient outcomes and advancing precision medicine.

Indexed as

cancercancer diagnosticscirculating tumor cells (CTC)circulating tumor DNA (ctDNA)liquid biopsyprecision oncology

Identifiers

PMID41602544
PMCPMC12832364

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.