Evidence map›Paper›PMID 31925342›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2020

Prognostic and predictive value of cell cycle progression (CCP) score in ductal carcinoma in situ of the breast.

Matteo Lazzeroni, Andrea DeCensi, Aliana Guerrieri-Gonzaga, Eleonora Pagan, Vincenzo Bagnardi, Debora Macis, Davide Serrano, Andrea Vingiani, Giuseppina Bonizzi, Massimo Barberis and 5 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2020. 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 48% 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, 7 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

15 authors at 6 institutions in 3 countries.

Matteo Lazzeroni *Division of Cancer Prevention and Genetics, IEO, European Institute of Oncology IRCCS, Milan, Italy. matteo.lazzeroni@ieo.it.ORCID http://orcid.org/0000-0002-2162-4002
Andrea DeCensi *Division of Medical Oncology, E.O. Ospedali Galliera, Genoa, Italy.
Aliana Guerrieri-GonzagaDivision of Cancer Prevention and Genetics, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Eleonora PaganDepartment of Statistics and Quantitative Methods, University of Milano-Bicocca, Milan, Italy.ORCID http://orcid.org/0000-0002-6788-394X
Vincenzo BagnardiDepartment of Statistics and Quantitative Methods, University of Milano-Bicocca, Milan, Italy.
Debora MacisDivision of Cancer Prevention and Genetics, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Davide SerranoDivision of Cancer Prevention and Genetics, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Andrea VingianiDepartment of Pathology, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Giuseppina BonizziDepartment of Pathology, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Massimo BarberisDepartment of Pathology, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Giancarlo PruneriDepartment of Pathology, IRCCS Istituto Nazionale Tumori, Milan, Italy.
Susanne WagnerMyriad Genetics, Salt Lake City, UT, USA.
Sara GandiniMolecular and Pharmaco-Epidemiology Unit, IEO, European Institute of Oncology IRCCS, Milan, Italy.ORCID http://orcid.org/0000-0002-1348-4548
Giuseppe VialeDepartment of Pathology, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Bernardo BonanniDivision of Cancer Prevention and Genetics, IEO, European Institute of Oncology IRCCS, Milan, Italy.
European Institute of Oncology · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Milan · ITUniversity of Milano-Bicocca · ITMyriad Genetics · USQueen Mary University of London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The natural history of ductal carcinoma in situ (DCIS) is highly variable and difficult to predict. Biomarkers are needed to stratify patients with DCIS for adjuvant therapy. We investigated the prognostic and predictive relevance of cell cycle progression (CCP) score in women with DCIS. We measured the expression of 23 genes involved in CCP with quantitative RT-PCR on RNA extracted from formalin-fixed paraffin-embedded tumor samples, and assessed the correlation of a predefined score with histopathologic features and recurrence. The signature was analyzed in a cohort of 909 consecutive DCIS with full histopathological features treated in a single institution. The main outcome measure was ipsilateral breast event (IBE) as first event observed, be it in situ or invasive. Median follow-up time was 8.7 years (IQR 6.5-10.5 years). There were 150 ipsilateral IBEs, 84 (56%) of which were invasive. In the first 5 years of follow-up, the score provided statistically different findings (p = 0.009), with IBE rates of 14.7% (95% CI, 10.4-19.7) for the highest quartile of CCP score (Q4) and 8.7% (95% CI, 6.7-11.0) for the lowest quartiles (Q1-3). The prognostic value for IBEs approached significance also in women treated with mastectomy (adjusted hazard ratio [HR] Q4 vs. Q1-3 = 2.60; 95% CI: 0.96-7.08; P = 0.06). Radiotherapy provided a greater benefit in women with higher CCP score. In addition, Q4 predicted a different risk after tamoxifen depending on menopausal status, with a beneficial trend on IBEs in postmenopausal women (HR 0.30; 95% CI, 0.07-1.39), and an opposite trend in premenopausal women (HR 1.68; 95% CI, 0.38-7.44) (P-interaction = 0.03). The results of this study provide for the first time the evidence that CCP score is a prognostic marker, which, after additional validation, could have an important role in personalizing the management of DCIS.

Indexed as

BreastBreast NeoplasmsCarcinoma, Intraductal, NoninfiltratingCell CycleDatabases, FactualFemaleFollow-Up StudiesHumansMastectomy, SegmentalNeoplasm Recurrence, LocalPrognosis

Identifiers

PMID31925342
OpenAlexW2998813475

What OpenQuestion holds

Textmetadata
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.