Evidence map›Paper›PMID 35569033›Full record

ArticleInternational journal of experimental pathology2022

Pre-analytical processing protocol of breast biopsies affects multigene panel results.

Vanessa Reinaldo Lima, Beatriz da Costa Aguiar Alves, Fernando Luiz Affonso Fonseca, Debora Krutman Zveibil, Auro Del Giglio

Abstract read
In one paragraph

Article in International journal of experimental pathology, 2022. 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
–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

1 citing paper in PubMed.

  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

5 authors.

Vanessa Reinaldo LimaClinical Analysis Laboratory of the Medical School of the ABC (FMABC) University Center, Santo André, Brazil.
Beatriz da Costa Aguiar AlvesClinical Analysis Laboratory of the Medical School of the ABC (FMABC) University Center, Santo André, Brazil.ORCID 0000-0001-9930-7747
Fernando Luiz Affonso FonsecaClinical Analysis Laboratory of the Medical School of the ABC (FMABC) University Center, Santo André, Brazil.ORCID 0000-0003-1223-1589
Debora Krutman ZveibilDepartment of Pathology, Medical School of the ABC (FMABC) University Center, Santo André, Brazil.ORCID 0000-0002-3252-6192
Auro Del GiglioDiscipline of Oncology and Hematology, Medical School of the ABC (FMABC) University Center, Santo André, Brazil.ORCID 0000-0002-2009-824X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The creation of multigene panels for prognostic and predictive purposes allows a more accurate indication of adjuvant chemotherapy for patients with breast cancer. In a previous study, we reproduced a multigene panel of 21 genes based on the commercial Oncotype-DX method. We submitted 183 embedded specimens obtained from breast surgery on patients with locoregional disease (stages I to III) between 2005 and 2010 performed at the Hospitals of the Medical School of the ABC Foundation. When we analysed the correlations between the score of the multigene panel and the progression-free interval (PFI) in all patients, we did not find a statistically significant association. However, when we selected only the 71 samples that had amplification of at least eight non-housekeeping genes, we observed that those with scores above the 75th percentile had a significantly lower PFI (p = .0054). Samples processed with nonbuffered formaldehyde were associated with a worse quality of extracted RNA (p = .004) and a significantly higher multigene panel score (p = .021). We conclude that variations in the pre-analytical processing of specimens destined for multigene panel amplification can significantly affect the results, with a potential impact on clinical management.

Indexed as

Breast NeoplasmsNeoplasm Recurrence, LocalBiopsyChemotherapy, AdjuvantFemaleGene Expression ProfilingHumansPrognosismultigene panelneoplasiaprognosisrecurrence score

Identifiers

PMID35569033
PMCPMC9107605

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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.