Evidence map›Paper›PMID 39107471›Full record

SynthesisScientific reports2024

Systematic review and feasibility study on pre-analytical factors and genomic analyses on archival formalin-fixed paraffin-embedded breast cancer tissue.

Dimitrios Salgkamis, Emmanouil G Sifakis, Susanne Agartz, Valtteri Wirta, Johan Hartman, Jonas Bergh, Theodoros Foukakis, Alexios Matikas, Ioannis Zerdes

Abstract readSystematic Review
In one paragraph

Synthesis in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
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

9 authors.

Dimitrios SalgkamisDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden. dimitrios.salgkamis@ki.se.
Emmanouil G SifakisDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Susanne AgartzDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Valtteri WirtaDepartment of Microbiology, Tumor and Cell Biology, Clinical Genomics Stockholm, Science for Life Laboratory, Karolinska Institutet, Stockholm, Sweden.
Johan HartmanDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Jonas BerghDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Theodoros FoukakisDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Alexios MatikasDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Ioannis ZerdesDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Formalin-fixed paraffin-embedded (FFPE) tissue represents a valuable source for translational cancer research. However, the widespread application of various downstream methods remains challenging. Here, we aimed to assess the feasibility of a genomic and gene expression analysis workflow using FFPE breast cancer (BC) tissue. We conducted a systematic literature review for the assessment of concordance between FFPE and fresh-frozen matched tissue samples derived from patients with BC for DNA and RNA downstream applications. The analytical performance of three different nucleic acid extraction kits on FFPE BC clinical samples was compared. We also applied a newly developed targeted DNA Next-Generation Sequencing (NGS) 370-gene panel and the nCounter BC360® platform on simultaneously extracted DNA and RNA, respectively, using FFPE tissue from a phase II clinical trial. Of the 3701 initial search results, 40 articles were included in the systematic review. High degree of concordance was observed in various downstream application platforms. Moreover, the performance of simultaneous DNA/RNA extraction kit was demonstrated with targeted DNA NGS and gene expression profiling. Exclusion of variants below 5% variant allele frequency was essential to overcome FFPE-induced artefacts. Targeted genomic analyses were feasible in simultaneously extracted DNA/RNA from FFPE material, providing insights for their implementation in clinical trials/cohorts.

Indexed as

Breast NeoplasmsFeasibility StudiesFormaldehydeGenomicsParaffin EmbeddingTissue FixationFemaleGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansFormaldehydeBreast cancerFormalin-fixed Paraffin-embeddedGene expressionNext-generation sequencingPreanalytical factors

Identifiers

PMID39107471
PMCPMC11303707

What OpenQuestion holds

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LicenceCC BY
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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.