Evidence map›Paper›PMID 41468688›Full record

ArticleESMO open2026

Evaluating MRI response criteria in microsatellite instability-high rectal cancer treated with immune checkpoint inhibitors.

Q Vanderbecq, R Cohen, M Camus, X Dray, Y Parc, T André, M Wagner

Abstract read
In one paragraph

Article in ESMO open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Q VanderbecqDepartment of Radiology, AP-HP, Sorbonne, Saint-Antoine Hospital, Paris, France; UMR 7371, Université Sorbonne, CNRS, Inserm U114615, Paris, France.
R CohenDepartment of Medical Oncology, AP-HP, Sorbonne, Saint-Antoine Hospital, Paris, France; INSERM UMRS 938, Équipe Instabilité des Microsatellites et Cancer, SIRIC CURAMUS, Centre de recherche Saint Antoine, Paris, France.
M CamusCentre for Digestive Endoscopy, AP-HP, Sorbonne, Saint-Antoine Hospital, Paris, France.
X DrayCentre for Digestive Endoscopy, AP-HP, Sorbonne, Saint-Antoine Hospital, Paris, France.
Y ParcDepartment of Digestive Surgery, AP-HP, Sorbonne, Saint-Antoine Hospital, Paris, France.
T AndréDepartment of Medical Oncology, AP-HP, Sorbonne, Saint-Antoine Hospital, Paris, France; INSERM UMRS 938, Équipe Instabilité des Microsatellites et Cancer, SIRIC CURAMUS, Centre de recherche Saint Antoine, Paris, France. Electronic address: thierry.andre@aphp.fr.
M WagnerDepartment of Radiology, AP-HP, Sorbonne, Saint-Antoine Hospital, Paris, France; UMR 7371, Université Sorbonne, CNRS, Inserm U114615, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs), particularly anti-programmed cell death protein 1 (PD-1) agents, have enabled consideration of non-operative management in patients with microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) rectal cancer. Standard magnetic resonance imaging (MRI) response criteria-developed for chemoradiotherapy-may not accurately reflect treatment effects with ICIs, however. PATIENTS AND

methodsWe retrospectively analyzed 14 patients with locally advanced MSI-H/dMMR rectal adenocarcinoma treated with neoadjuvant anti-PD-1 monotherapy. All patients achieved a complete pathological response. MRI assessment included T2-weighted, diffusion-weighted, and contrast-enhanced sequences. Treatment response was defined as complete pathological response by surgical pathology (proctectomy), or by endoscopic and biopsy-confirmed complete remission (watch-and-wait strategy).

resultsMRI showed distinct post-treatment patterns: split scar sign (n = 2), fibrotic response (n = 5), lesion disappearance (n = 1), and residual intermediate T2 signal (n = 6). All mucinous tumors retained T2-hyperintense residues. In select cases, fibrotic response was beyond 3 months. In two surgical cases, histological analysis revealed residual mucinous material without viable tumor cells.

conclusionsMRI response patterns after anti-PD-1 monotherapy in MSI-H/dMMR rectal cancer differ from those observed after radiochemotherapy, suggesting the need to adapt current imaging criteria for accurate response assessment and informed surgical decision making. Persistent MRI abnormalities are frequent despite complete pathological response, and warrant cautious interpretation in the ICI setting.

Indexed as

Immune Checkpoint InhibitorsMagnetic Resonance ImagingMicrosatellite InstabilityRectal NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeImmune Checkpoint InhibitorsimmunotherapyMRIrectal tumor

Identifiers

PMID41468688
PMCPMC12804033

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