Evidence map›Paper›PMID 42717454›Full record

ArticleRomanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie

Beyond H&E: CDX2 immunohistochemistry in tumor budding assessment of colorectal carcinoma.

Aminia Diana Ciobănoiu, Gheorghe Gindrovel Dumitra, Iancu Emil Pleşea, Anwar Erchid, Valentin Titus Grigorean

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Article in Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 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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5 · Who and what money

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5 authors.

Aminia Diana CiobănoiuDepartment of Family Medicine, University of Medicine and Pharmacy of Craiova, Romania; gindrovel.dumitra@umfcv.ro; Departments of Pathology, Carol Davila University of Medicine and Pharmacy, and Bagdasar-Arseni Emergency Clinical Hospital, Bucharest, Romania; emil.plesea@umfcd.ro.
Gheorghe Gindrovel Dumitra
Iancu Emil Pleşea
Anwar Erchid
Valentin Titus Grigorean

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesTumor budding (TB) phenomenon is recognized as one of the important adverse prognostic factors of colorectal carcinoma (CRC) and is currently assessed following to the International Tumor Budding Consensus Conference (ITBCC) recommendations on routine Hematoxylin and Eosin (H&E)-stained slides. However, TB evaluation may become difficult in cases showing inflammatory infiltrates, stromal desmoplasia, or glandular fragmentation. Immunohistochemical (IHC) markers, including caudal type homeobox 2 (CDX2), may improve the identification of isolated tumor buds in such situations. PATIENTS, MATERIALS AND

methodsThe retrospective study included 170 CRC cases selected from the archives of a single regional pathology center. TB was evaluated on both H&E-stained and CDX2-immunostained slides according to a modified ITBCC-based grading system including an additional Bd0 category for cases lacking identifiable tumor buds. Tumor buds were counted within a standardized field area. TB distribution was evaluated in the proximal, middle, and distal tumor regions.

resultsLow-grade budding lesions predominated in all evaluated tumor regions on both H&E and CDX2 assessment. Regional variation in TB distribution was observed along the invasive tumor front, supporting the presence of spatial heterogeneity in CRC. Comparative analysis of TB evaluation on H&E-stained preparations and on CDX2 immunolabeled preparations revealed the existence of differences between the two methods, especially in cases with low or intermediate budding activity. CDX2 immunostaining facilitated the identification of additional tumor buds, leading to the reclassification of a number of cases to higher budding categories (intermediary and high-grade budding lesions), especially in difficult cases, characterized by intense stromal reaction, inflammation or glandular fragmentation.

conclusionsThe present study demonstrated that IHC labeling should be considered primarily as a detection tool for accurate TB assessment, but other antibodies should be tested to increase the accuracy of tumor bud identification.

Indexed as

CDX2 Transcription FactorColorectal NeoplasmsEosine Yellowish-(YS)HematoxylinImmunohistochemistryAgedFemaleHumansMaleMiddle AgedRetrospective StudiesCDX2 protein, humanCDX2 Transcription FactorEosine Yellowish-(YS)Hematoxylincolon adenocarcinomahistopathologylarynxmucinous adenocarcinomatumor architecturetumor grading

Identifiers

PMID42717454
PMCPMC13657412

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