Evidence map›Paper›PMID 41438843›Full record

ArticleThe journal of liquid biopsy2025

Cancer in a drop: Liquid biopsy highlights from the World Conference on Lung Cancer (WCLC) 2025.

Nadia Ghazali, Ana Ortega-Franco, Diego de Miguel-Perez, Erick F Saldanha, Konstantinos Venetis, Pasquale Pisapia, Surbhi Singhal, Benjamin A Bleiberg, Carolina Reduzzi, Roberto Borea

Abstract read
In one paragraph

Article in The journal of liquid biopsy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
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

10 authors.

Nadia GhazaliInternational Society of Liquid Biopsy (ISLB) Young Committee, Spain.
Ana Ortega-FrancoInternational Society of Liquid Biopsy (ISLB) Young Committee, Spain.
Diego de Miguel-PerezGENYO Centre for Genomics and Oncological Research: Pfizer, University of Granada, Andalusian Regional Government, Liquid Biopsy and Cancer Interception Group, Granada, Spain.
Erick F SaldanhaDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Konstantinos VenetisDivision of Pathology, European Institute of Oncology IRCCS, Milan, Italy.
Pasquale PisapiaDepartment of Public Health, University of Naples Federico II, Naples, Italy.
Surbhi SinghalDivision of Hematology/Oncology, Department of Medicine, University of California, Davis, California, USA.
Benjamin A BleibergDivision of Hematology and Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, USA.
Carolina ReduzziInternational Society of Liquid Biopsy (ISLB) Young Committee, Spain.
Roberto BoreaInternational Society of Liquid Biopsy (ISLB) Young Committee, Spain.

Funding

UC Davis Paul Calabresi K12 Clinical Oncology Research Career Development ProgramK12CA138464 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BIRKELAND, ANDREW CHARLES, LARA, PRIMO N. · 2011 to 2025
$11.4M
NCI NIH HHS K12 CA138464
6 · The paper itself

Abstract

The role of liquid biopsy in oncological care continues to expand, with multiple studies presented at the International Association for the Study of Lung Cancer (IASLC) 2025 World Conference on Lung Cancer (WCLC 2025). This review summarizes recent advances in liquid biopsy for thoracic oncology, encompassing both non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC). In early detection and screening, proteomic profiling has identified potential biomarkers predictive of future lung cancer risk. The integration of proteomics with clinical and imaging data can improve pulmonary nodule malignancy prediction. In resectable NSCLC, tumour-informed whole-genome sequencing (WGS) assay demonstrated high sensitivity for minimal residual disease (MRD) detection, with MRD clearance following neoadjuvant osimertinib or chemo-immunotherapy associated with favorable outcomes. In advanced NSCLC, longitudinal liquid biopsy analyses reveal dynamic subclonal evolution driving early treatment resistance. Circulating tumor DNA (ctDNA) clearance following targeted therapy in MET exon 14 skipping and BRAF-mutated tumors was associated with improved clinical outcomes. Emerging biomarkers such as ctDNA tumour fraction and circulating microRNA signatures are promising for radiotherapy stratification and prediction of immunotherapy-related toxicities. In SCLC, MRD monitoring enables earlier detection of disease progression and supports ctDNA-guided selection of patients for consolidation immunotherapy following chemotherapy. Overall, these advances demonstrate the expanding role of liquid biopsy in improving early detection, guiding treatment, and improving disease monitoring in lung cancer.

Indexed as

Circulating tumor DNALiquid biopsyLung cancerMinimal residual diseaseNon-small cell lung cancerSmall cell lung cancer

Identifiers

PMID41438843
PMCPMC12720026

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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.