Evidence map›Paper›PMID 35565423›Full record

ArticleCancers2022

Blood Eosinophils Are Associated with Efficacy of Targeted Therapy in Patients with Advanced Melanoma.

Simone Wendlinger, Jonas Wohlfarth, Sophia Kreft, Claudia Siedel, Teresa Kilian, Ulrich Dischinger, Markus V Heppt, Kilian Wistuba-Hamprecht, Friedegund Meier, Matthias Goebeler and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. An Itch Receptor Drives Melanoma.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Atopy Improves Survival and Decreases Risk of Brain Metastasis in Cutaneous Melanoma.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2025
    Article
  4. Review
  5. Innate Immune Cells in Melanoma: Implications for Immunotherapy.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. 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

14 authors at 5 institutions in 1 country.

Simone WendlingerDepartment of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.
Jonas WohlfarthDepartment of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.
Sophia KreftDepartment of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.
Claudia SiedelDepartment of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.
Teresa KilianDepartment of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.
Ulrich DischingerDepartment of Endocrinology and Diabetology, University Hospital Würzburg, 97080 Würzburg, Germany.
Markus V HepptDepartment of Dermatology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.ORCID 0000-0003-4603-1825
Kilian Wistuba-HamprechtDepartment of Dermatology, University Hospital Tübingen, 72076 Tübingen, Germany.ORCID 0000-0002-3104-8512
Friedegund MeierDepartment of Dermatology, University Hospital Carl Gustav Carus at the Technical University Dresden, 01307 Dresden, Germany.
Matthias GoebelerDepartment of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.ORCID 0000-0001-7095-9848
Dirk SchadendorfDepartment of Dermatology, University Hospital, University of Duisburg-Essen and German Cancer Consortium, Partner Site Essen, 45147 Essen, Germany.ORCID 0000-0003-3524-7858
Anja GesierichDepartment of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.
Corinna KosnopfelDepartment of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.ORCID 0000-0002-0910-838X
Bastian SchillingDepartment of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.ORCID 0000-0001-8859-4103
Universitätsklinikum Würzburg · DEDeutschen Konsortium für Translationale Krebsforschung · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity Children's Hospital Tübingen · DEUniversity Hospital Carl Gustav Carus · DE

Funding

Deutsche Forschungsgemeinschaft SCHI 1344/2-1Klaus Tschira Foundation 00.316.2017
6 · The paper itself

Abstract

backgroundEosinophils appear to contribute to the efficacy of immunotherapy and their frequency was suggested as a predictive biomarker. Whether this observation could be transferred to patients treated with targeted therapy remains unknown.

methodsBlood and serum samples of healthy controls and 216 patients with advanced melanoma were prospectively and retrospectively collected. Freshly isolated eosinophils were phenotypically characterized by flow cytometry and co-cultured in vitro with melanoma cells to assess cytotoxicity. Soluble serum markers and peripheral blood counts were used for correlative studies.

resultsEosinophil-mediated cytotoxicity towards melanoma cells, as well as phenotypic characteristics, were similar when comparing healthy donors and patients. However, high relative pre-treatment eosinophil counts were significantly associated with response to MAPKi (

conclusionHigh pre-treatment eosinophil counts in advanced melanoma patients were associated with a significantly improved response to MAPKi. Functionally, eosinophils show potent cytotoxicity towards melanoma cells, which can be reinforced by MAPKi. Further studies are needed to unravel the molecular mechanisms of our observations.

Indexed as

biomarkereosinophilsmelanoma

Identifiers

PMID35565423
PMCPMC9104271
OpenAlexW4225432536

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.