Evidence map›Paper›PMID 42352538›Full record

ArticleCancers2026

Diagnostic Challenges of Tumor Tissue and Circulating Microsatellite Status Assessment in Metastatic Colorectal Cancer and Their Impact on Access to Immunotherapy: A Real-World Retrospective Study.

Benoist Chibaudel, Linda Dainese, Elisabeth Carola, Perrine Goyer, Hubert Richa, Arnaud Saget, Olivier Oberlin, Hélène Marijon, Nathalie Perez-Staub, Aimery de Gramont and 2 more

Abstract read
In one paragraph

Article in Cancers, 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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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

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

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

12 authors.

Benoist ChibaudelDepartment of Medical Oncology, Hôpital Franco-Britannique-Fondation Cognacq-Jay, Cancérologie Paris Ouest, 92300 Levallois-Perret, France.ORCID 0000-0003-1279-2044
Linda DaineseDepartment of Pathology and Molecular Biology, IHP Group-Paris, 92240 Malakoff, France.
Elisabeth CarolaDepartment of Medical Oncology, Groupe Hospitalier du Sud de l'Oise, 60100 Creil, France.
Perrine GoyerDepartment Digestive Surgery, Groupe Hospitalier Privé Ambroise Paré-Hartmann, 92100 Neuilly sur Seine, France.
Hubert RichaDepartment Digestive Surgery, Groupe Hospitalier Privé Ambroise Paré-Hartmann, 92100 Neuilly sur Seine, France.
Arnaud SagetDepartment Digestive Surgery, Groupe Hospitalier Privé Ambroise Paré-Hartmann, 92100 Neuilly sur Seine, France.
Olivier OberlinDepartment Digestive Surgery, Groupe Hospitalier Privé Ambroise Paré-Hartmann, 92100 Neuilly sur Seine, France.
Hélène MarijonDepartment of Medical Oncology, Hôpital Franco-Britannique-Fondation Cognacq-Jay, Cancérologie Paris Ouest, 92300 Levallois-Perret, France.
Nathalie Perez-StaubDepartment of Medical Oncology, Hôpital Franco-Britannique-Fondation Cognacq-Jay, Cancérologie Paris Ouest, 92300 Levallois-Perret, France.
Aimery de GramontCancérologie Paris Ouest, 92300 Levallois-Perret, France.
Alain ToledanoDepartment of Radiotherapy, Hartmann Oncology Radiotherapy Group, Cancérologie Paris Ouest, 92300 Levallois-Perret, France.
Pascal PujolDepartment of Genetic, Centre Hospitalier Universitaire de Montpellier, 34090 Montpellier, France.ORCID 0000-0001-8315-4715

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicrosatellite instability (MSI) and mismatch repair (MMR) deficiency are key predictive biomarkers for immune checkpoint inhibitors (ICIs) in metastatic colorectal cancer (mCRC). In real-world practice, however, diagnostic pathways often involve heterogeneous testing modalities, which may lead to discordant or inconclusive results.

methodsWe conducted a retrospective study of patients with mCRC who underwent at least one MSI/MMR assessment between 2015 and 2025. Diagnostic modalities included IHC, tissue-based and liquid-based MSI testing. A predefined decision algorithm classified results as conclusive or inconclusive; discordant cases underwent adjudication that integrated a pathology review, molecular features, and technical considerations. Patients were ultimately assigned to definitive MSS or definitive MSI groups. Clinical characteristics, treatment patterns, and outcomes-particularly in relation to immunotherapy-were evaluated.

resultsAmong 727 evaluable patients, the MSI/MMR status was conclusive in 695 (95.6%) and inconclusive in 32 (4.4%). Inconclusive cases resulted from isolated MMR protein loss, heterogeneous or equivocal staining, inter-tumoral discordance, or discrepancies between tissue- and liquid-based assays. After adjudication, 54 patients (7.4%) were classified as definitive MSI and 673 (92.6%) as definitive MSS. Definitive MSI tumors were associated with female sex, right-sided primaries, high-grade histology, nodal involvement, and BRAF V600E mutations. Among the definitive MSI patients, 31 (57.4%) received immunotherapy, achieving a complete response rate of 48.4% and an overall response rate of 71.0%. Median PFS and OS were not reached in the definitive MSI group, whereas definitive MSS patients treated with ICIs experienced significantly poorer outcomes. Conclusive and adjudicated MSI groups demonstrated comparable responses to immunotherapy.

conclusionsIn real-world practice, a meaningful proportion (4%) of mCRC patients experience inconclusive MSI/MMR assessment, with important clinical implications. Both technical and biological factors contribute to diagnostic uncertainty. Integrating orthogonal testing modalities and applying structured adjudication improves classification accuracy and ensures appropriate access to immunotherapy.

Indexed as

diagnostic discordanceimmunotherapymetastatic colorectal cancermicrosatellite instabilitymismatch repairreal-world evidence

Identifiers

PMID42352538
PMCPMC13296429

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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.