Evidence map›Paper›PMID 35513610›Full record

ArticleVirchows Archiv : an international journal of pathology2022

Acellular mucin in lymph nodes isolated from treatment-naïve colorectal cancer resections: a clinicopathologic analysis of 16 cases.

James E Lapinski, Alok A Khorana, Lisa Rybicki, Canan Firat, Hwajeong Lee, Kathryn Piotti, Eugene H Lewis, Michael McNamara, Vikram Deshpande, Jinru Shia and 1 more

Open access · greenAbstract read
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2022. 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
0.4field-weighted citation impact, top 39% of its field
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, 2 citations in OpenAlex.

  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

11 authors at 8 institutions in 1 country.

James E LapinskiDepartment of Anatomic Pathology, Cleveland Clinic, Cleveland, OH, USA.
Alok A KhoranaDepartment of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH, USA.
Lisa RybickiDepartment of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
Canan FiratDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Hwajeong LeeDepartment of Pathology and Laboratory Medicine, Albany Medical Center, Albany, NY, USA.
Kathryn PiottiDepartment of Pathology, Morristown Medical Center, Morristown, NJ, USA.
Eugene H LewisDepartment of Pathology, St. Vincent's Medical Center, Bridgeport, CT, USA.
Michael McNamaraDepartment of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH, USA.
Vikram DeshpandeDepartment of Pathology, Massachusetts General Hospital, Boston, MA, USA.
Jinru ShiaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Deepa T PatilDepartment of Anatomic Pathology, Cleveland Clinic, Cleveland, OH, USA. dtpatil@bwh.harvard.edu.ORCID http://orcid.org/0000-0001-7837-1299
Cleveland Clinic · USMemorial Sloan Kettering Cancer Center · USAlbany Medical Center Hospital · USBrigham and Women's Hospital · USCleveland Clinic Lerner College of Medicine · USMassachusetts General Hospital · USMorristown Medical Center · USSt. Vincent's Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Lymph nodes with acellular mucin harvested from treated colorectal cancers (CRC) are staged as pN0. However, there is variability among pathologists while reporting the pN stage when acellular mucin is found within nodes of untreated CRCs. While the UICC guidelines suggest staging them as pN1, the AJCC and CAP do not offer any recommendations. In order to characterize their clinicopathologic features and outcome, we compared 16 untreated CRCs (study group; mean age: 68 years) harboring nodes with acellular mucin with 34 pN0 and 25 pN1 untreated CRC controls. All tumors were unifocal; 12 (75%) were right-sided lesions. Most cases (75%) showed one node with acellular mucin (range: 1-3). MMR-deficient tumors were significantly more common in the study group (83%) compared to pN0 (33%; p = 0.006) and pN1 controls (8%; p < 0.001). The overall survival of study group patients was closer to pN0 compared to pN1 controls; however, this difference was not statistically significant. In conclusion, untreated CRC that harbor acellular mucin within lymph nodes commonly present as right-sided, MMR-deficient tumors in older women that show a non-mucinous phenotype. While the limited number of cases precludes us from making any formal recommendations about staging, we suggest that the finding of acellular mucin in a node should prompt evaluation of deeper levels (with or without cytokeratin immunohistochemistry) and submission of all pericolonic fat for additional lymph node harvest. Whether acellular mucin in nodes of untreated CRCs is related to the indolent biology of the disease, a robust local immune response or MMR deficiency requires further investigation.

Indexed as

Colorectal NeoplasmsMucinsAgedFemaleHumansLymphatic MetastasisLymph NodesNeoplasm StagingMucinsAcellular mucinColon cancerLymph nodesUntreated

Identifiers

PMID35513610
PMCPMC9979094
OpenAlexW4228998636

What OpenQuestion holds

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Registered trials

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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.