Evidence map›Paper›PMID 40647439›Full record

ArticleCancers2025

Performance and Prognostic Relevance of Lymph Node Assessment by One-Step Nucleic Acid Amplification Assay in Rectal Cancer: A Multicenter Study.

Qing Liu, Sandra Lopez-Prades, Karmele Saez de Gordoa, Maite Rodrigo-Calvo, Mireia Garcia, Juan Ruiz Martin, Angel Romo, Ignacio Pinilla, Jordi Tarragona, Begoña Otero Alen and 3 more

Abstract read
In one paragraph

Article in Cancers, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Qing LiuAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), 08036 Barcelona, Spain.ORCID 0000-0003-1784-6400
Sandra Lopez-PradesAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), 08036 Barcelona, Spain.ORCID 0000-0001-8208-2959
Karmele Saez de GordoaAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), 08036 Barcelona, Spain.ORCID 0000-0001-8106-6121
Maite Rodrigo-CalvoAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), 08036 Barcelona, Spain.ORCID 0000-0001-6675-3425
Mireia GarciaPathology Department, Hospital Clinic Barcelona, 08036 Barcelona, Spain.ORCID 0000-0003-3445-9744
Juan Ruiz MartinPathology Department, Hospital Universitario de Toledo, 45004 Toledo, Spain.
Angel RomoPathology Department, Hospital Universitario de Toledo, 45004 Toledo, Spain.ORCID 0000-0002-7094-8484
Ignacio PinillaPathology Department, Hospital Universitario Severo Ochoa, 28911 Madrid, Spain.ORCID 0000-0002-6120-8302
Jordi TarragonaPathology Department, Hospital Universitari Arnau de Vilanova, 25198 Lleida, Spain.ORCID 0000-0002-1459-4087
Begoña Otero AlenPathology Department, University Hospital Complex A Coruña (CHUAC), 15006 A Coruña, Spain.ORCID 0000-0002-2876-6732
Jordi CampsAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), 08036 Barcelona, Spain.
Ivan ArchillaAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), 08036 Barcelona, Spain.ORCID 0000-0002-2142-0608
Miriam CuatrecasasAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), 08036 Barcelona, Spain.ORCID 0000-0003-3063-0110

Funding

Agència de Gestió d'Ajuts Universitaris i de Recerca 2017 SGR 1035China Scholarship Council 202208320022Instituto de Salud Carlos III PI20800863
6 · The paper itself

Abstract

BACKGROUND/

objectivesLymph node metastases (LNM) undetected by standard hematoxylin and eosin (H&E) have been associated with unfavorable prognosis in colorectal cancer. The One-Step Nucleic Acid Amplification (OSNA) assay has demonstrated superior sensitivity in detecting LNM compared to H&E. We aimed to assess the performance of OSNA in detecting LNM, as well as its prognostic value in rectal cancer (RC) patients.

methodsLymph nodes (LNs) of patients from 15 centers were analyzed by both H&E and OSNA. The total tumor load (TTL) was defined as the sum of cytokeratin 19 mRNA copies/µL in all LNs from a surgical specimen, using a threshold of 250 copies/μL for OSNA positivity. Cox proportional hazard regression was used to assess the effect of TTL ≥ 250 or 6000 copies/μL on cancer-specific survival (CSS) and recurrence-free survival (RFS), with Firth's method applied to account for low event rate.

resultsA total of 97 RC patients were included. Of these, 84 patients were eligible for survival analysis. The sensitivity and specificity of OSNA, compared to H&E, were 91.7% and 84.7%, respectively. TTL ≥ 6000 versus <6000 copies/μL was related to worse CSS and RFS. When dividing TTL into three groups: ≤250, 250-6000, and >6000 copies/μL, only TTL ≥ 6000 copies/μL was significantly associated with worse CSS and RFS.

conclusionsThe OSNA assay is highly sensitive for detecting LNM in RC patients. A TTL of ≥6000 copies/μL could identify a subset of RC patients with worse CSS and RFS who might benefit from adjuvant treatment or intensive surveillance.

Indexed as

diagnosislymph node metastasesOSNAprognosisrectal carcinomastaging

Identifiers

PMID40647439
PMCPMC12249117

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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.