Evidence map›Paper›PMID 30861338›Full record

ArticleCancer cytopathology2019

Cytomorphologic and molecular analyses of fallopian tube fimbrial brushings for diagnosis of serous tubal intraepithelial carcinoma.

M Herman Chui, Russell Vang, Tian-Li Wang, Ie-Ming Shih, Christopher J VandenBussche

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cytopathology, 2019. 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, top 97% 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, 3 citations in OpenAlex.

  1. Article
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

5 authors at 1 institution in 1 country.

M Herman ChuiDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.ORCID 0000-0002-7220-3996
Russell VangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Tian-Li WangDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Ie-Ming ShihDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Christopher J VandenBusscheDepartment of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland.ORCID 0000-0002-8822-5655
Johns Hopkins University · US

Funding

SPORE in Ovarian CancerP50CA228991 · NCI · JOHNS HOPKINS UNIVERSITY · PI Tian-Li Wang · 2018 to 2026
$20.5M
CIHRNCI NIH HHS P50 CA228991
6 · The paper itself

Abstract

backgroundThe paradigm shift localizing the origin of ovarian high-grade serous carcinoma (HGSC) to the fallopian tube underscores the rationale for meticulous microscopic examination of salpingectomy specimens. The precursor, termed "serous tubal intraepithelial carcinoma," is often a focal lesion, which poses difficulties for histologic diagnosis.

methodsThe authors describe a method to examine exfoliated epithelial cells from fallopian tube fimbria by gentle brushing, thereby enabling thorough sampling of the mucosal surface. Fimbrial brushings were collected from 20 fresh salpingectomy specimens from 15 patients, including 5 who had pathologically confirmed ovarian HGSC. Samples taken only from tubes that were grossly negative for tumor were processed for Papanicolaou staining, p53 immunocytochemistry, and tumor protein 53 (TP53) mutation analysis.

resultsCells with malignant cytomorphologic features were identified only in tubal brushings from patients with ovarian HGSC. In all cases, atypical/malignant cells on cytology corresponded to lesions with similar morphology and immunostaining pattern in permanent sections, demonstrating the sensitivity of the technique while providing reassurance that specimen integrity was not disrupted by the procedure. Targeted next-generation sequencing confirmed the presence of TP53 mutations in fimbrial brushings from HGSC, but not in benign samples, and demonstrated concordance with the immunostaining pattern. Identical mutations were observed in matched lesions microdissected from formalin-fixed tissue sections.

conclusionsThe described technique enables cytologic evaluation of the fallopian tube fimbria for a diagnosis of serous tubal intraepithelial carcinoma, serving as a complement to histology while offering distinct advantages with respect to the procurement of cellular material for ancillary testing and research.

Indexed as

Carcinoma in SituCell Surface ExtensionsCystadenocarcinoma, SerousDNA Mutational AnalysisEpithelial CellsFallopian Tube NeoplasmsFallopian TubesFemaleHumansImmunohistochemistryMutationOvarian NeoplasmsSalpingectomySensitivity and SpecificityTumor Suppressor Protein p53Tumor Suppressor Protein p53exfoliative cytologyfallopian tubeovarian cancerprecursor lesiontubal brushing

Identifiers

PMID30861338
PMCPMC8352790
OpenAlexW2921658426

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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.