Evidence map›Paper›PMID 42467114›Full record

ArticleInternational journal of colorectal disease2026

Evaluating the usefulness of 18F-FDG PET/MR in rectal cancer staging: a prospective comparison with histopathological findings.

Rafał Maksim, Dominika Hempel, Małgorzata Mojsak, Justyna Śliwowska-Burzyńska, Konrad Zuzda, Patryk Gugnacki, Iwona Sidorkiewicz, Ewa Sierko

Abstract readComparative Study
In one paragraph

Article in International journal of colorectal disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

8 authors.

Rafał MaksimDepartment of Radiotherapy, Maria Skłodowska-Curie Białystok Oncology Center, Bialystok, 15-027, Poland.
Dominika HempelDepartment of Radiotherapy I, Maria Skłodowska-Curie Białystok Oncology Center, Bialystok, 15-027, Poland.
Małgorzata MojsakIndependent Laboratory of Molecular Imaging, Medical University of Bialystok, Bialystok, 15-276, Poland.
Justyna Śliwowska-BurzyńskaDepartment of Radiology, Maria Skłodowska-Curie Bialystok Oncology Center, Bialystok, 15-027, Poland.
Konrad ZuzdaDepartment of Anesthesiology and Intensive Care, National Medical Institute of The Ministry of Interior and Administration, Warsaw, 02-507, Poland.
Patryk GugnackiDepartment of Otolaryngology and Maxillofacial Surgery, Jędrzej Śniadecki Regional Specialist Hospital, Bialystok, 15-278, Poland.
Iwona SidorkiewiczClinical Research Support Centre, Medical University of Białystok, Białystok, 15-276, Poland.
Ewa SierkoDepartment of Radiotherapy I, Maria Skłodowska-Curie Białystok Oncology Center, Bialystok, 15-027, Poland. esierko@onkologia.bialystok.pl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate preoperative staging of rectal cancer (RC) is essential for treatment planning. MRI is the standard for local assessment but has limitations in evaluating nodal involvement and tumor deposits. Hybrid PET/MR combines morphological and metabolic imaging and may improve staging accuracy. This study assessed PET/MR performance in RC and regional lymph nodes staging compared with histopathology.

methodsSixteen patients with biopsy-proven rectal cancer underwent PET/MR with ^18F-FDG. Tumor size, T stage, nodal status, and tumor deposits were evaluated using multiparametric MR sequences (T1, T2, diffusion-weighted, contrast-enhanced) combined with PET. Imaging findings were compared to histopathological results. Diagnostic performance metrics, including accuracy, sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV), were calculated with corresponding 95% confidence intervals.

resultsPET/MR accurately staged the primary tumor in 81.25% of cases (95% CI: 57.0-93.4), with sensitivity of 100%, specificity of 50.0%, PPV of 76.9%, and NPV of 100% for advanced T-stage assessment. Three cT3 tumors were downstaged to pT2; no tumors were upstaged. For nodal staging based on ESGAR criteria, diagnostic accuracy was 75.0% (95% CI: 50.5-89.8), with sensitivity of 57.1%, specificity of 88.9%, PPV of 80.0%, and NPV of 72.7%. Tumor deposits were not detected on imaging but were present in four specimens. Incidental findings included a biopsy-confirmed breast adenocarcinoma and one benign thyroid lesion.

conclusion18F-FDG PET/MR shows potential for accurate assessment of the primary tumor and reliable exclusion of advanced T-stage disease. However, its performance in nodal staging and tumor deposit detection remains limited. Given the small sample size and potential confounding from preoperative radiotherapy, these findings should be considered hypothesis-generating and require validation in larger prospective cohorts.

Indexed as

Fluorodeoxyglucose F18Magnetic Resonance ImagingMultimodal ImagingPositron-Emission TomographyRectal NeoplasmsAgedFemaleHumansMaleMiddle AgedNeoplasm StagingProspective StudiesFluorodeoxyglucose F18PET/MRRectal cancerStaging

Identifiers

PMID42467114
PMCPMC13658387

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.