Evidence map›Paper›PMID 35768550›Full record

ArticleBritish journal of cancer2022

Comprehensive multiplexed immune profiling of the ductal carcinoma in situ immune microenvironment regarding subsequent ipsilateral invasive breast cancer risk.

Mathilde M Almekinders, Tycho Bismeijer, Tapsi Kumar, Fei Yang, Bram Thijssen, Rianne van der Linden, Charlotte van Rooijen, Shiva Vonk, Baohua Sun, Edwin R Parra Cuentas and 17 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. GermlineImmuno-oncology technology · 2026
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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

27 authors at 4 institutions in 2 countries.

Mathilde M AlmekindersDivision of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0002-1554-2887
Tycho BismeijerDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0001-6514-4767
Tapsi KumarDepartment of Genomic Medicine, MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0003-2825-3387
Fei YangDepartment of Translational Molecular Pathology, MD Anderson Cancer Center, Houston, TX, USA.
Bram ThijssenDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0003-1562-2649
Rianne van der LindenDepartment of Pathology, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Charlotte van RooijenDepartment of Pathology, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Shiva VonkDepartment of Pathology, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Baohua SunDepartment of Translational Molecular Pathology, MD Anderson Cancer Center, Houston, TX, USA.
Edwin R Parra CuentasDepartment of Translational Molecular Pathology, MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0001-9068-1636
Ignacio I WistubaDepartment of Translational Molecular Pathology, MD Anderson Cancer Center, Houston, TX, USA.
Savitri KrishnamurthyDepartment of Pathology, MD Anderson Cancer Center, Houston, TX, USA.
Lindy L VisserDivision of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0001-7856-1981
Iris M SeignetteDepartment of Pathology, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Ingrid HoflandCore Facility Molecular Pathology and Biobanking, Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Joyce SandersDepartment of Pathology, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.ORCID 0000-0002-0551-7813
Annegien BroeksCore Facility Molecular Pathology and Biobanking, Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Jason K LoveBreast Surgical Oncology, MD Anderson Cancer Center, Houston, TX, USA.
Brian MenegazDepartment of Surgery, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0002-3020-5790
Lodewyk WesselsDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Alastair M ThompsonDivision of Surgical Oncology, Baylor College of Medicine, Houston, TX, USA.
Karin E de VisserOncode Institute, Utrecht, The Netherlands.
Erik HooijbergDepartment of Pathology, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Esther LipsDivision of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0003-3488-4935
Andrew FutrealDepartment of Genomic Medicine, MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0001-8663-2671
Jelle WesselingDivision of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands. j.wesseling@nki.nl.ORCID 0000-0002-8940-2676
Grand Challenge PRECISION Consortium
The Netherlands Cancer Institute · NLThe University of Texas MD Anderson Cancer Center · USLeiden University Medical Center · NLBaylor College of Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDuctal carcinoma in situ (DCIS) is treated to prevent subsequent ipsilateral invasive breast cancer (iIBC). However, many DCIS lesions will never become invasive. To prevent overtreatment, we need to distinguish harmless from potentially hazardous DCIS. We investigated whether the immune microenvironment (IME) in DCIS correlates with transition to iIBC.

methodsPatients were derived from a Dutch population-based cohort of 10,090 women with pure DCIS with a median follow-up time of 12 years. Density, composition and proximity to the closest DCIS cell of CD20

resultsHigher stromal density of analysed immune cell subsets was significantly associated with higher grade, ER negativity, HER-2 positivity, Ki67 ≥ 14%, periductal fibrosis and comedonecrosis (P < 0.05). Density, composition and proximity to the closest DCIS cell of all analysed immune cell subsets did not differ between cases and controls.

conclusionIME features analysed by mIF in 141 patients from a well-annotated cohort of pure DCIS with long-term follow-up are no predictors of subsequent iIBC, but do correlate with other factors (grade, ER, HER2 status, Ki-67) known to be associated with invasive recurrences.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, Intraductal, NoninfiltratingBiomarkers, TumorCD8-Positive T-LymphocytesFemaleForkhead Transcription FactorsHumansKi-67 AntigenTumor MicroenvironmentBiomarkers, TumorForkhead Transcription FactorsKi-67 Antigen

Identifiers

PMID35768550
PMCPMC9519539
OpenAlexW4283759178

What OpenQuestion holds

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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.