Evidence map›Paper›PMID 41335335›Full record

ReviewPathologie (Heidelberg, Germany)2026

Fourier transform mid-infrared imaging and rapid evaporative ionization mass spectrometry imaging in FFPE colorectal adenocarcinoma samples.

B Borkovits, Cs Török, E Kontsek, A Pesti, K Havasi, J Slezsák, Sz Gergely, B Medgyes, I Csabai, A Kiss and 1 more

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Review in Pathologie (Heidelberg, Germany), 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

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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

11 authors.

B BorkovitsDepartment of Biological Physics, ELTE Eötvös Loránd University, Budapest, Hungary.
Cs TörökDepartment of Applied Biotechnology and Food Science, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Budapest, Hungary.
E KontsekDepartment of Pathology, Forensic and Insurance Medicine, Semmelweis University, Üllői út 93, 1091, Budapest, Hungary. kontsek.endre@semmelweis.hu.
A PestiDepartment of Pathology, Forensic and Insurance Medicine, Semmelweis University, Üllői út 93, 1091, Budapest, Hungary.
K HavasiDepartment of Applied Mechanics, Faculty of Mechanical Engineering, Budapest University of Technology and Economics, Budapest, Hungary.
J SlezsákDepartment of Applied Biotechnology and Food Science, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Budapest, Hungary.
Sz GergelyDepartment of Applied Biotechnology and Food Science, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Budapest, Hungary.
B MedgyesDepartment of Electronics Technology, Faculty of Electrical Engineering and Informatics, Budapest University of Technology and Economics, Budapest, Hungary.
I CsabaiDepartment of Physics of Complex Systems, ELTE Eötvös Loránd University, Budapest, Hungary.
A KissDepartment of Pathology, Forensic and Insurance Medicine, Semmelweis University, Üllői út 93, 1091, Budapest, Hungary.
P PollnerDepartment of Biological Physics, ELTE Eötvös Loránd University, Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHungary ranks highest in the world regarding both the incidence and death rates of colorectal cancer. Novel analytical methods have surfaced in the past decade and are infiltrating the field of medicine. Infrared spectroscopy (IR) and mass spectrometry (MS) are frequently used for such measurements; however, multimodal techniques resulting from the combination of these have not yet gained widespread adoption.

methodsTissue microarray (TMA) of colorectal adenocarcinomas, liver metastases, and surrounding colon tissues were prepared at the Institute of Pathology, Forensic, and Insurance Medicine, Semmelweis University. From the block, 2‑ and 10-µm sections were cut for infrared and MS imaging, respectively. Infrared measurements were performed with a Perkin Elmer Spotlight microscope (Perkin Elmer Inc., Waltham, MA, USA) on samples with an area of 2200 × 2200 µm

resultsThe spectral results from the samples were noise filtered in both methods to separate the sample signal from the background. Overall, 41 cores were suitable for further data processing. For the measurements with infrared spectroscopy, the three-class classification resulted in accuracy of 0.71 and 0.71 using C‑support vector classification (SVC) and eXtreme Gradient Boosting (XGBoost) algorithms. For the analysis of the mass spectrometry data, 0.65 and 0.70 accuracy values were observed.

conclusionIdentical TMA slides have been imaged with two analytical methods. The performance of the separating algorithms was very close, which underscores the efficacy of the spectroscopy and spectrometry approach. A vector database of the spectra could be combined with the whole-slide image pixels obtained by a traditional digital scanner. A further step could be a thickness-optimized measurement, which would determine the setting for the combined measurement of the exact same sample.

Indexed as

AdenocarcinomaColorectal NeoplasmsMass SpectrometryFormaldehydeHumansLiver NeoplasmsParaffin EmbeddingSpectroscopy, Fourier Transform InfraredTissue Array AnalysisTissue FixationFormaldehydeAluminum-coatedCancerREIMSSection thicknessTMA

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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.