Evidence map›Paper›PMID 35267459›Full record

ArticleCancers2022

Differences in the Molecular Profile between Primary Breast Carcinomas and Their Cutaneous Metastases.

Silvia González-Martínez, David Pizarro, Belén Pérez-Mies, Tamara Caniego-Casas, José Luis Rodríguez-Peralto, Giuseppe Curigliano, Alfonso Cortés, María Gión, Javier Cortés, José Palacios

Abstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

10 authors.

Silvia González-MartínezClinical Research, Ramón y Cajal Hospital, 28034 Madrid, Spain.ORCID 0000-0002-8139-8369
David PizarroMolecular Pathology of Cancer Group, Ramón y Cajal Health Research Institute (IRYCIS), 28034 Madrid, Spain.ORCID 0000-0002-8945-9541
Belén Pérez-MiesMolecular Pathology of Cancer Group, Ramón y Cajal Health Research Institute (IRYCIS), 28034 Madrid, Spain.
Tamara Caniego-CasasMolecular Pathology of Cancer Group, Ramón y Cajal Health Research Institute (IRYCIS), 28034 Madrid, Spain.
José Luis Rodríguez-PeraltoCentre for Biomedical Research in Cancer Networks (CIBERONC), Carlos III Health Institute, 28029 Madrid, Spain.ORCID 0000-0002-6578-7153
Giuseppe CuriglianoEuropean Institute of Oncology, Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), 20141 Milan, Italy.ORCID 0000-0003-1781-2518
Alfonso CortésDepartment of Medical Oncology, Ramón y Cajal University Hospital, 28034 Madrid, Spain.
María GiónDepartment of Medical Oncology, Ramón y Cajal University Hospital, 28034 Madrid, Spain.
Javier CortésCentre for Biomedical Research in Cancer Networks (CIBERONC), Carlos III Health Institute, 28029 Madrid, Spain.ORCID 0000-0001-7623-1583
José PalaciosMolecular Pathology of Cancer Group, Ramón y Cajal Health Research Institute (IRYCIS), 28034 Madrid, Spain.ORCID 0000-0002-6730-5066

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe characterization of molecular alterations of primary breast carcinomas (BC) and their cutaneous metastases (CM) to identify genes involved in the metastatic process have not yet been completely accomplished.

methodsTo investigate the molecular alterations of BC and their CM, a total of 66 samples (33 BC and 33 CM) from 33 patients were analyzed by immunohistochemical and massive parallel sequencing analyses. In addition, the clinicopathological characteristics of patients and tumors were analyzed.

resultsTriple negative (TN) BCs were overrepresented (36.4%) among tumors that developed CM. A change of tumor surrogate molecular type in metastases was found in 15% of patients and 48.5% of the CM presented some additional molecular alteration with respect to the primary tumor, the most frequent were amplification of

conclusionsThe TN molecular type has a greater risk of developing skin metastases. There are phenotypic changes and additional molecular alterations in skin metastases compared to the corresponding primary breast tumors in nearly half of the patients. Although these changes do not follow a specific pattern and varied from patient to patient, they could impact on the treatment. More studies with larger patient and sample cohorts are needed.

Indexed as

breast cancerimmunohistochemistrymetastasismutationsNGSpathologyskin

Identifiers

PMID35267459
PMCPMC8909188

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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.