Evidence map›Paper›PMID 37445849›Full record

ArticleInternational journal of molecular sciences2023

Combining Solid and Liquid Biopsy for Therapy Monitoring in Esophageal Cancer.

Florian Richter, Clara Henssen, Tim Alexander Steiert, Tobias Meissner, Anne-Sophie Mehdorn, Christoph Röcken, Andre Franke, Jan-Hendrik Egberts, Thomas Becker, Susanne Sebens and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. ctDNA responds to neoadjuvant treatment in locally advanced rectal cancer.Journal of cancer research and clinical oncology · 2024
    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

11 authors at 4 institutions in 2 countries.

Florian RichterDepartment of General and Thoracic Surgery, University Hospital Schleswig-Holstein Campus Kiel, 24105 Kiel, Germany.ORCID 0000-0001-6190-9259
Clara HenssenInstitute of Clinical Molecular Biology, Kiel University, 24105 Kiel, Germany.
Tim Alexander SteiertInstitute of Clinical Molecular Biology, Kiel University, 24105 Kiel, Germany.
Tobias MeissnerDepartment of Molecular and Experimental Medicine, Avera Cancer Institute, Sioux Falls, SD 57105, USA.ORCID 0000-0002-9680-7153
Anne-Sophie MehdornDepartment of General and Thoracic Surgery, University Hospital Schleswig-Holstein Campus Kiel, 24105 Kiel, Germany.ORCID 0000-0003-4415-8371
Christoph RöckenDepartment of Pathology, University Hospital Schleswig-Holstein Campus Kiel, 24105 Kiel, Germany.ORCID 0000-0002-6989-8002
Andre FrankeInstitute of Clinical Molecular Biology, Kiel University, 24105 Kiel, Germany.
Jan-Hendrik EgbertsDepartment of Surgery, Israelitisches Krankenhaus Hamburg, 22297 Hamburg, Germany.
Thomas BeckerDepartment of General and Thoracic Surgery, University Hospital Schleswig-Holstein Campus Kiel, 24105 Kiel, Germany.
Susanne SebensInstitute for Experimental Cancer Research, Kiel University, University Hospital Schleswig-Holstein Campus Kiel, 24105 Kiel, Germany.
Michael ForsterInstitute of Clinical Molecular Biology, Kiel University, 24105 Kiel, Germany.ORCID 0000-0001-9927-5124
Christian-Albrechts-Universität zu Kiel · DEUniversity Hospital Schleswig-Holstein · DEAvera Health · USIsraelitisches Krankenhaus · DE

Funding

Competence Centre for Genomic Analysis, Kiel (CCGA) 874719European Advanced Infrastructure for Innovative Genomics, EASI-Genomics 824110German Federal Ministry of Educatoin and Research 01EY1103
6 · The paper itself

Abstract

Esophageal cancer (EC) has one of the highest mortality rates among cancers, making it imperative that therapies are optimized and dynamically adapted to individuals. In this regard, liquid biopsy is an increasingly important method for residual disease monitoring. However, conflicting detection rates (14% versus 60%) and varying cell-free circulating tumor DNA (ctDNA) levels (0.07% versus 0.5%) have been observed in previous studies. Here, we aim to resolve this discrepancy. For 19 EC patients, a complete set of cell-free DNA (cfDNA), formalin-fixed paraffin-embedded tumor tissue (TT) DNA and leukocyte DNA was sequenced (139 libraries). cfDNA was examined in biological duplicates and/or longitudinally, and TT DNA was examined in technical duplicates. In baseline cfDNA, mutations were detected in 12 out of 19 patients (63%); the median ctDNA level was 0.4%. Longitudinal ctDNA changes were consistent with clinical presentation. Considerable mutational diversity was observed in TT, with fewer mutations in cfDNA. The most recurrently mutated genes in TT were

Indexed as

Circulating Tumor DNAEsophageal NeoplasmsBiomarkers, TumorDNA, NeoplasmHomeodomain ProteinsHumansLiquid BiopsyMutationBiomarkers, TumorCirculating Tumor DNADNA, NeoplasmHomeodomain ProteinsTSHZ3 protein, humancell-free DNAcfDNAcirculating tumor DNActDNAECNGSsequencingSETBP1

Identifiers

PMID37445849
PMCPMC10341643
OpenAlexW4382459762

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.