Evidence map›Paper›PMID 41930304›Full record

ArticleESMO real world data and digital oncology2026

Liquid biopsies using circulating tumor DNA for surveillance of gastrointestinal cancers in Hispanics: first real-world data report.

C Cardona-De Jesús, H Centeno-Girona, F Garau-Rolón, H Melero-Rodríguez, I Alicea, M Cruz-Correa

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Article in ESMO real world data and digital oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

C Cardona-De JesúsDr. Isaac Gonzalez Martinez Oncology Hospital, San Juan, USA.
H Centeno-GironaUniversity of Puerto Rico Medical Sciences Campus, San Juan, USA.
F Garau-RolónDr. Isaac Gonzalez Martinez Oncology Hospital, San Juan, USA.
H Melero-RodríguezDr. Isaac Gonzalez Martinez Oncology Hospital, San Juan, USA.
I AliceaDr. Isaac Gonzalez Martinez Oncology Hospital, San Juan, USA.
M Cruz-CorreaDr. Isaac Gonzalez Martinez Oncology Hospital, San Juan, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Malignant tumors release circulating tumor DNA (ctDNA) into the bloodstream, providing insights into tumor-specific mutations and pathways driving cancer progression. ctDNA testing is currently approved as a type of liquid biopsy to monitor disease burden and detect minimal residual disease (MRD). This study aimed to evaluate the adoption of ctDNA testing in a community oncology practice and assess the overall diagnostic performance of ctDNA and its association with disease progression in stage IV colorectal cancer (CRC), as determined by imaging studies. Patients and methods: This retrospective study analyzed the medical records of 88 patients with gastrointestinal cancers (80 CRC, 5 gastric, 3 esophageal) who underwent ctDNA molecular testing between January 2020 and April 2022. Electronic medical records from patients aged ≥21 years who had two or more ctDNA tests with concurrent imaging studies or a pathology-confirmed CRC, gastric cancer, or esophageal cancer diagnosis were evaluated. Results: At baseline, 47 (53.4%) patients had negative and 41 (46.6%) had positive results. Most patients had CRC (90.1%). In stage IV CRC, ctDNA was increasing before radiologic progression in all documented cases (100%), with a median lead time of 2.5 months (range 0.5-15 months). In early-stage CRC (I-III), ctDNA preceded radiologic progression in 40% of cases, with a median lead time of 6 months (range 6-10 months). Conclusions: Using real-world data, we report the first-time results of the ctDNA testing adoption in a community oncology setting among patients with gastrointestinal cancers, predominantly CRC. Our findings suggest that integration of ctDNA testing may support disease monitoring in routine clinical practice.

Indexed as

cancer monitoringliquid biopsymolecular diagnosticsnon-invasive biomarkersprecision oncologytumor surveillance

Identifiers

PMID41930304
PMCPMC13040887

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