Evidence map›Paper›PMID 32734520›Full record

ArticleBreast cancer research and treatment2020

Prognostic value of histopathological DCIS features in a large-scale international interrater reliability study.

Emma J Groen, Jan Hudecek, Lennart Mulder, Maartje van Seijen, Mathilde M Almekinders, Stoyan Alexov, Anikó Kovács, Ales Ryska, Zsuzsanna Varga, Francisco-Javier Andreu Navarro and 22 more

Open access · hybridAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

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  18. Low-risk DCIS. What is it? Observe or excise?Virchows Archiv : an international journal of pathology · 2022
    Review
  19. Morphological intratumor heterogeneity in ductal carcinoma in situ of the breast.Virchows Archiv : an international journal of pathology · 2021
    Article
  20. 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

32 authors at 20 institutions in 11 countries.

Emma J GroenDepartment of Pathology, Netherlands Cancer Institute - Antoni van Leeuwenhoek, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands.
Jan HudecekDepartment of Research IT, Netherlands Cancer Institute - Antoni van Leeuwenhoek, Amsterdam, The Netherlands.
Lennart MulderDepartment of Molecular Pathology, Netherlands Cancer Institute - Antoni van Leeuwenhoek, Amsterdam, The Netherlands.
Maartje van SeijenDepartment of Molecular Pathology, Netherlands Cancer Institute - Antoni van Leeuwenhoek, Amsterdam, The Netherlands.
Mathilde M AlmekindersDepartment of Molecular Pathology, Netherlands Cancer Institute - Antoni van Leeuwenhoek, Amsterdam, The Netherlands.
Stoyan AlexovDepartment of Pathology, Oncology Hospital, Sofia, Bulgaria.
Anikó KovácsDepartment of Clinical Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Ales RyskaThe Fingerland Department of Pathology, Charles University Medical Faculty and University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Zsuzsanna VargaInstitute of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
Francisco-Javier Andreu NavarroAtryshealth Co, S.L., Barcelona, Spain.
Simonetta BianchiDivision of Pathological Anatomy, Department of Health Sciences, University of Florence, Florence, Italy.
Willem VreulsDepartment of Pathology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.
Eva BalslevDepartment of Pathology, Herlev University Hospital, Herlev, Denmark.
Max V BootDepartment of Pathology, Amsterdam University Medical Center, Location VUmc, Amsterdam, The Netherlands.
Janina Kulka2nd Department of Pathology, Semmelweis University, Budapest, Hungary.
Ewa ChmielikTumor Pathology Department, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Gliwice, Poland.
Ellis BarbéDepartment of Pathology, Amsterdam University Medical Center, Location VUmc, Amsterdam, The Netherlands.
Mathilda J de RooijSymbiant Pathology Expert Centre, Location ZMC, Zaandam, The Netherlands.
Winand VosDepartment of Pathology, Zuyderland Medical Center, Location Sittard-Geleen, Sittard-Geleen, The Netherlands.
Andrea FarkasDepartment of Pathology, Gävle Hospital, Gävle, Sweden.
Natalja E Leeuwis-FedorovichDepartment of Pathology, Deventer Hospital, Deventer, The Netherlands.
Peter RegitnigDiagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Austria.
Pieter J WestenendLaboratory for Pathology Dordrecht, Dordrecht, The Netherlands.
Loes F S KooremanDepartment of Pathology and GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, The Netherlands.
Cecily QuinnDepartment of Pathology and Laboratory Medicine, St. Vincent's University Hospital, Dublin, Ireland.
Giuseppe FlorisLaboratory of Translational Cell & Tissue Research, Department of Imaging and Pathology, KU Leuven - University of Leuven, Leuven, Belgium.
Gábor CserniDepartment of Pathology, Bács-Kiskun County Teaching Hospital, Kecskemét, Hungary.
Paul J van DiestDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
Esther H LipsDepartment of Molecular Pathology, Netherlands Cancer Institute - Antoni van Leeuwenhoek, Amsterdam, The Netherlands.
Michael SchaapveldDivision of Psychosocial Research and Epidemiology, Netherlands Cancer Institute - Antoni van Leeuwenhoek, Amsterdam, The Netherlands.
Jelle WesselingDepartment of Pathology, Netherlands Cancer Institute - Antoni van Leeuwenhoek, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands. j.wesseling@nki.nl.ORCID http://orcid.org/0000-0002-8940-2676
Grand Challenge PRECISION consortium
Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital · NLAmsterdam University Medical Centers · NLCanisius-Wilhelmina Ziekenhuis · NLCharles University · CZDeventer Ziekenhuis · NLGävle Hospital · SEHerlev Hospital · DKKU Leuven · BEMaastricht University Medical Centre · NLMedical University of Graz · ATSahlgrenska University Hospital · SESemmelweis University · HUSt. Vincent's University Hospital · IEThe Maria Sklodowska-Curie National Research Institute of Oncology · PLUniversity Hospital of Zurich · CHUniversity Medical Center Utrecht · NLUniversity of Florence · ITUniversity of Szeged · HUZaans Medisch Centrum · NLZuyderland Medisch Centrum · NL

Funding

Cancer Research UK and KWF Kankerbestrijding in a joint grant C38317/A24043KWF Kankerbestrijding NKI2014-7167
6 · The paper itself

Abstract

purposeFor optimal management of ductal carcinoma in situ (DCIS), reproducible histopathological assessment is essential to distinguish low-risk from high-risk DCIS. Therefore, we analyzed interrater reliability of histopathological DCIS features and assessed their associations with subsequent ipsilateral invasive breast cancer (iIBC) risk.

methodsUsing a case-cohort design, reliability was assessed in a population-based, nationwide cohort of 2767 women with screen-detected DCIS diagnosed between 1993 and 2004, treated by breast-conserving surgery with/without radiotherapy (BCS ± RT) using Krippendorff's alpha (KA) and Gwet's AC2 (GAC2). Thirty-eight raters scored histopathological DCIS features including grade (2-tiered and 3-tiered), growth pattern, mitotic activity, periductal fibrosis, and lymphocytic infiltrate in 342 women. Using majority opinion-based scores for each feature, their association with subsequent iIBC risk was assessed using Cox regression.

resultsInterrater reliability of grade using various classifications was fair to moderate, and only substantial for grade 1 versus 2 + 3 when using GAC2 (0.78). Reliability for growth pattern (KA 0.44, GAC2 0.78), calcifications (KA 0.49, GAC2 0.70) and necrosis (KA 0.47, GAC2 0.70) was moderate using KA and substantial using GAC2; for (type of) periductal fibrosis and lymphocytic infiltrate fair to moderate estimates were found and for mitotic activity reliability was substantial using GAC2 (0.70). Only in patients treated with BCS-RT, high mitotic activity was associated with a higher iIBC risk in univariable analysis (Hazard Ratio (HR) 2.53, 95% Confidence Interval (95% CI) 1.05-6.11); grade 3 versus 1 + 2 (HR 2.64, 95% CI 1.35-5.14) and a cribriform/solid versus flat epithelial atypia/clinging/(micro)papillary growth pattern (HR 3.70, 95% CI 1.34-10.23) were independently associated with a higher iIBC risk.

conclusionsUsing majority opinion-based scores, DCIS grade, growth pattern, and mitotic activity are associated with iIBC risk in patients treated with BCS-RT, but interrater variability is substantial. Semi-quantitative grading, incorporating and separately evaluating nuclear pleomorphism, growth pattern, and mitotic activity, may improve the reliability and prognostic value of these features.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, Intraductal, NoninfiltratingFemaleHumansMastectomy, SegmentalNeoplasm Recurrence, LocalPrognosisReproducibility of ResultsDuctal carcinoma in situInterrater reliabilityInvasive breast cancerRisk stratification

Identifiers

PMID32734520
PMCPMC7497690
OpenAlexW3046175168

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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.