Evidence map›Paper›PMID 38278927›Full record

ArticleScientific reports2024

Towards effectiveness of cell free DNA based liquid biopsy in head and neck squamous cell carcinoma.

Ewelina Kowal-Wisniewska, Katarzyna Jaskiewicz, Anna Bartochowska, Katarzyna Kiwerska, Adam Ustaszewski, Tomasz Gorecki, Maciej Giefing, Jaroslaw Paluszczak, Malgorzata Wierzbicka, Malgorzata Jarmuz-Szymczak

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Immune biomarkers for head and neck cancer.Cancer immunology, immunotherapy : CII · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. 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

10 authors at 5 institutions in 1 country.

Ewelina Kowal-WisniewskaInstitute of Human Genetics, Polish Academy of Sciences, Strzeszynska 32, 60-479, Poznan, Poland. ewelina.kowal@igcz.poznan.pl.
Katarzyna JaskiewiczInstitute of Human Genetics, Polish Academy of Sciences, Strzeszynska 32, 60-479, Poznan, Poland.
Anna BartochowskaDepartment of Otolaryngology and Laryngeal Oncology, Poznan University of Medical Sciences, Poznan, Poland.
Katarzyna KiwerskaInstitute of Human Genetics, Polish Academy of Sciences, Strzeszynska 32, 60-479, Poznan, Poland.
Adam UstaszewskiInstitute of Human Genetics, Polish Academy of Sciences, Strzeszynska 32, 60-479, Poznan, Poland.
Tomasz GoreckiFaculty of Mathematics and Computer Science, Adam Mickiewicz University, Poznan, Poland.
Maciej GiefingInstitute of Human Genetics, Polish Academy of Sciences, Strzeszynska 32, 60-479, Poznan, Poland.
Jaroslaw PaluszczakDepartment of Pharmaceutical Biochemistry, Poznan University of Medical Sciences, Poznan, Poland.
Malgorzata WierzbickaInstitute of Human Genetics, Polish Academy of Sciences, Strzeszynska 32, 60-479, Poznan, Poland.
Malgorzata Jarmuz-SzymczakInstitute of Human Genetics, Polish Academy of Sciences, Strzeszynska 32, 60-479, Poznan, Poland.
Polish Academy of Sciences · PLPoznan University of Medical Sciences · PLAdam Mickiewicz University in Poznań · PLInstitute of Human Genetics · PLWrocław University of Science and Technology · PL

Funding

Narodowe Centrum Badań i Rozwoju POIR.04.01.04-00-0003/17-00
6 · The paper itself

Abstract

Liquid biopsy is a minimally invasive procedure, that uses body fluids sampling to detect and characterize cancer fingerprints. It is of great potential in oncology, however there are challenges associated with the proper handling of liquid biopsy samples that need to be addressed to implement such analysis in patients' care. Therefore, in this study we performed optimization of pre-analytical conditions and detailed characterization of cfDNA fraction (concentration, length, integrity score) in surgically treated HNSCC patients (n = 152) and healthy volunteers (n = 56). We observed significantly higher cfDNA concentration in patients compared to healthy controls (p < 0.0001) and a time dependent decrease of cfDNA concentration after tumor resection. Our results also revealed a significant increase of cfDNA concentration with age in both, healthy volunteers (p = 0.04) and HNSCC patients (p = 0.000002). Moreover, considering the multitude of HNSCC locations, we showed the lack of difference in cfDNA concentration depending on the anatomical location. Furthermore, we demonstrated a trend toward higher cfDNA length (range 35-10380 and 500-10380 bp) in the group of patients with recurrence during follow-up. In conclusion, our study provide a broad characterization of cfDNA fractions in HNSCC patients and healthy controls. These findings point to several aspects necessary to consider when implementing liquid biopsy in clinical practice including: (I) time required for epithelial regeneration to avoid falsely elevated levels of cfDNA not resulting from active cancer, (II) age-related accumulation of nucleic acids accompanied by less efficient elimination of cfDNA and (III) higher cfDNA length in patients with recurrence during follow-up, reflecting predominance of tumor necrosis.

Indexed as

Cell-Free Nucleic AcidsHead and Neck NeoplasmsBiomarkers, TumorHumansLiquid BiopsySpecimen HandlingSquamous Cell Carcinoma of Head and NeckBiomarkers, TumorCell-Free Nucleic Acids

Identifiers

PMID38278927
PMCPMC10817923
OpenAlexW4391252306

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Registered trials

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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.