Evidence map›Paper›PMID 34614346›Full record

ArticleJournal of pathology and translational medicine2021

A multicenter study of interobserver variability in pathologic diagnosis of papillary breast lesions on core needle biopsy with WHO classification.

Hye Ju Kang, Sun Young Kwon, Ahrong Kim, Woo Gyeong Kim, Eun Kyung Kim, Ae Ree Kim, Chungyeul Kim, Soo Kee Min, So Young Park, Sun Hee Sung and 16 more

Abstract read
In one paragraph

Article in Journal of pathology and translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Invasive papillary carcinoma of the breast.Frontiers in oncology · 2024
    Review
  3. 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

26 authors.

Hye Ju KangDepartment of Pathology, National Cancer Center, Goyang, Korea.
Sun Young KwonDepartment of Pathology, Keimyung University Dongsan Medical Center, Daegu, Korea.
Ahrong KimDepartment of Pathology, Pusan National University Hospital, Busan, Korea.
Woo Gyeong KimDepartment of Pathology, Inje University Haeundae Paik Hospital, Busan, Korea.
Eun Kyung KimDepartment of Pathology, Eulji University Hospital, Seoul, Korea.
Ae Ree KimDepartment of Pathology, Korea University Guro Hospital, Seoul, Korea.
Chungyeul KimDepartment of Pathology, Korea University Guro Hospital, Seoul, Korea.
Soo Kee MinDepartment of Pathology, Hallym University Sacred Heart Hospital, Anyang, Korea.
So Young ParkDepartment of Pathology, MizMedi Hospital, Seoul, Korea.
Sun Hee SungDepartment of Pathology, Ewha Womans University Mokdong Hospital, Seoul, Korea.
Hye Kyoung YoonDepartment of Pathology, Inje University Busan Paik Hospital, Busan, Korea.
Ahwon LeeDepartment of Pathology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Ji Shin LeeDepartment of Pathology, Chonnam National University Hwasun Hospital, Hwasun, Korea.
Hyang Im LeeDepartment of Pathology, Gyeongsang National University Changwon Hospital, Changwon, Korea.
Ho Chang LeeDepartment of Pathology, Chungbuk National University Hospital, Cheongju, Korea.
Sung Chul LimDepartment of Pathology, Chosun University Hospital, Gwangju, Korea.
Sun Young JunDepartment of Pathology, Incheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Incheon, Korea.
Min Jung JungDepartment of Pathology, Kosin University Gospel Hospital, Busan, Korea.
Chang Won JungDepartment of Pathology, Green Cross Laboratories, Yongin, Korea.
Soo Youn ChoDepartment of Pathology, Sungkyunkwan University Samsung Medical Center, Seoul, Korea.
Eun Yoon ChoDepartment of Pathology, Sungkyunkwan University Samsung Medical Center, Seoul, Korea.
Hye Jeong ChoiDepartment of Pathology, Ulsan University Hospital, Ulsan, Korea.
So Yeon ParkDepartment of Pathology, Seoul National University Bundang Hospital, Seongnam, Korea.
Jee Yeon KimDepartment of Pathology, Pusan National University Yangsan Hospital, Yangsan, Korea.
In Ae ParkDepartment of Pathology, Seoul National University Hospital, Seoul, Korea.
Youngmee KwonDepartment of Pathology, National Cancer Center, Goyang, Korea.

Funding

Korean Society of Pathologists
6 · The paper itself

Abstract

backgroundPapillary breast lesions (PBLs) comprise diverse entities from benign and atypical lesions to malignant tumors. Although PBLs are characterized by a papillary growth pattern, it is challenging to achieve high diagnostic accuracy and reproducibility. Thus, we investigated the diagnostic reproducibility of PBLs in core needle biopsy (CNB) specimens with World Health Organization (WHO) classification.

methodsDiagnostic reproducibility was assessed using interobserver variability (kappa value, κ) and agreement rate in the pathologic diagnosis of 60 PBL cases on CNB among 20 breast pathologists affiliated with 20 medical institutions in Korea. This analysis was performed using hematoxylin and eosin (H&E) staining and immunohistochemical (IHC) staining for cytokeratin 5 (CK5) and p63. The pathologic diagnosis of PBLs was based on WHO classification, which was used to establish simple classifications (4-tier, 3-tier, and 2-tier).

resultsOn WHO classification, H&E staining exhibited 'fair agreement' (κ = 0.21) with a 47.0% agreement rate. Simple classifications presented improvement in interobserver variability and agreement rate. IHC staining increased the kappa value and agreement rate in all the classifications. Despite IHC staining, the encapsulated/solid papillary carcinoma (EPC/SPC) subgroup (κ = 0.16) exhibited lower agreement compared to the non-EPC/SPC subgroup (κ = 0.35) with WHO classification, which was similar to the results of any other classification systems.

conclusionsAlthough the use of IHC staining for CK5 and p63 increased the diagnostic agreement of PBLs in CNB specimens, WHO classification exhibited a higher discordance rate compared to any other classifications. Therefore, this result warrants further intensive consensus studies to improve the diagnostic reproducibility of PBLs with WHO classification.

Indexed as

Agreement rateCore needle biopsyInterobserver variabilityPapillary breast lesion

Identifiers

PMID34614346
PMCPMC8601955

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.