Evidence map›Paper›PMID 29733308›Full record

ArticleJournal of visualized experiments : JoVE2018

Therapy Testing in a Spheroid-based 3D Cell Culture Model for Head and Neck Squamous Cell Carcinoma.

Jan Hagemann, Christian Jacobi, Sabine Gstoettner, Christian Welz, Sabina Schwenk-Zieger, Roland Stauber, Sebastian Strieth, Julian Kuenzel, Philipp Baumeister, Sven Becker

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  10. Frontiers in oncology · 2022
    Review
  11. Review
  12. Article
  13. Organoids in Translational Oncology.Journal of clinical medicine · 2020
    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 2 countries.

Jan HagemannDepartment of Otorhinolaryngology, Johannes-Gutenberg University Medical Center; Jan.Hagemann@unimedizin-mainz.de.
Christian JacobiDepartment of Otorhinolaryngology, Technical University of Munich Medical Center.
Sabine GstoettnerDepartment of Otorhinolaryngology, Ludwig-Maximilian-University Medical Center.
Christian WelzDepartment of Otorhinolaryngology, University of Goettingen Medical Center.
Sabina Schwenk-ZiegerDepartment of Otorhinolaryngology, Ludwig-Maximilian-University Medical Center.
Roland StauberDepartment of Otorhinolaryngology, Johannes-Gutenberg University Medical Center.
Sebastian StriethDepartment of Otorhinolaryngology, Johannes-Gutenberg University Medical Center.
Julian KuenzelDepartment of Otorhinolaryngology, Johannes-Gutenberg University Medical Center.
Philipp BaumeisterDepartment of Otorhinolaryngology, Ludwig-Maximilian-University Medical Center.
Sven BeckerDepartment of Otorhinolaryngology, Johannes-Gutenberg University Medical Center; Department of Otorhinolaryngology, Ludwig-Maximilian-University Medical Center.
University Medical Center · USJohannes Gutenberg University Mainz · DEUniversity Medical Center of the Johannes Gutenberg University Mainz · DETechnical University of Munich · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current treatment options for advanced and recurrent head and neck squamous cell carcinoma (HNSCC) enclose radiation and chemo-radiation approaches with or without surgery. While platinum-based chemotherapy regimens currently represent the gold standard in terms of efficacy and are given in the vast majority of cases, new chemotherapy regimens, namely immunotherapy are emerging. However, the response rates and therapy resistance mechanisms for either chemo regimen are hard to predict and remain insufficiently understood. Broad variations of chemo and radiation resistance mechanisms are known to date. This study describes the development of a standardized, high-throughput in vitro assay to assess HNSCC cell line's response to various therapy regimens, and hopefully on primary cells from individual patients as a future tool for personalized tumor therapy. The assay is designed to being integrated into the quality-controlled standard algorithm for HNSCC patients at our tertiary care center; however, this will be subject of future studies. Technical feasibility looks promising for primary cells from tumor biopsies from actual patients. Specimens are then transferred into the laboratory. Biopsies are mechanically separated followed by enzymatic digestion. Cells are then cultured in ultra-low adhesion cell culture vials that promote the reproducible, standardized and spontaneous formation of three-dimensional, spheroid-shaped cell conglomerates. Spheroids are then ready to be exposed to chemo-radiation protocols and immunotherapy protocols as needed. The final cell viability and spheroid size are indicators of therapy susceptibility and therefore could be drawn into consideration in future to assess the patients' likely therapy response. This model could be a valuable, cost-efficient tool towards personalized therapy for head and neck cancer.

Indexed as

Carcinoma, Squamous CellCell Culture TechniquesHead and Neck NeoplasmsHumansPrecision MedicineSquamous Cell Carcinoma of Head and Neck

Identifiers

PMID29733308
PMCPMC6100693
OpenAlexW2799505078

What OpenQuestion holds

Textmetadata
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.