Evidence map›Paper›PMID 32110946›Full record

ArticleCancers2020

MDM2, MDM4 and EGFR Amplifications and Hyperprogression in Metastatic Acral and Mucosal Melanoma.

Andrea Forschner, Franz-Joachim Hilke, Irina Bonzheim, Axel Gschwind, German Demidov, Teresa Amaral, Stephan Ossowski, Olaf Riess, Christopher Schroeder, Peter Martus and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 4 pooled it
5.2field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 4 syntheses or guidelines pooled it, 81 citations in OpenAlex.

  1. Pooled it
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  3. Investigation on potential biomarkers of hyperprogressive disease (HPD) triggered by immune checkpoint inhibitors (ICIs).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
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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

15 authors at 5 institutions in 2 countries.

Andrea ForschnerCenter for Dermatooncology, Department of Dermatology, University Hospital Tübingen, 72076 Tübingen, Germany.
Franz-Joachim HilkeInstitute of Medical Genetics and Applied Genomics, University Hospital Tübingen, 72076 Tübingen, Germany.
Irina BonzheimInstitute of Pathology and Neuropathology, University Hospital Tübingen, 72076 Tübingen, Germany.
Axel GschwindInstitute of Medical Genetics and Applied Genomics, University Hospital Tübingen, 72076 Tübingen, Germany.
German DemidovInstitute of Medical Genetics and Applied Genomics, University Hospital Tübingen, 72076 Tübingen, Germany.
Teresa AmaralCenter for Dermatooncology, Department of Dermatology, University Hospital Tübingen, 72076 Tübingen, Germany.
Stephan OssowskiInstitute of Medical Genetics and Applied Genomics, University Hospital Tübingen, 72076 Tübingen, Germany.
Olaf RiessInstitute of Medical Genetics and Applied Genomics, University Hospital Tübingen, 72076 Tübingen, Germany.
Christopher SchroederInstitute of Medical Genetics and Applied Genomics, University Hospital Tübingen, 72076 Tübingen, Germany.
Peter MartusInstitute for Clinical Epidemiology and applied Biostatistics (IKEaB), 72076 Tuebingen, Germany.
Bernhard KlumppInstitute for Radiology, Rems-Murr-Kliniken, 71364 Winnenden, Germany.
Irene Gonzalez-MenendezInstitute of Pathology and Neuropathology, University Hospital Tübingen, 72076 Tübingen, Germany.
Claus GarbeCenter for Dermatooncology, Department of Dermatology, University Hospital Tübingen, 72076 Tübingen, Germany.
Heike NiessnerCenter for Dermatooncology, Department of Dermatology, University Hospital Tübingen, 72076 Tübingen, Germany.
Tobias SinnbergCenter for Dermatooncology, Department of Dermatology, University Hospital Tübingen, 72076 Tübingen, Germany.
University of Tübingen · DEBernstein Center for Computational Neuroscience Tübingen · DEUniversity Children's Hospital Tübingen · DEPortuguese Air Force Academy · PTRems-Murr-Klinikum · DE

Funding

Hiege Foundation Forschner_SinnbergTÜFF Habilitation Program for Women of the Faculty of Medicine Tübingen, Germany 2521-0-
6 · The paper itself

Abstract

backgroundMucosal and acral melanoma respond worse to immune checkpoint inhibitors (ICI) than cutaneous melanoma.

methodsWe conducted a query of our melanoma registry, looking for patients with metastatic acral or mucosal melanoma treated by ICI. Whole exome sequencing, FISH and immunohistochemistry on melanoma tissue could be performed on 45 of the total cohort of 51 patients. Data were correlated with patients` responses to ICI and survival.

results22 out of 51 patients had hyperprogressive disease (an increase in tumor load of >50% at the first staging). Hyperprogression occurred more often in case of

conclusionsSo far, we found no reliable predictive marker for patients who develop hyperprogression on ICI, specifically with regard to

Indexed as

acral melanomaEGFRhyperprogressionimmune checkpoint inhibitorsMDM2MDM4mucosal melanoma

Identifiers

PMID32110946
PMCPMC7139387
OpenAlexW3009008277

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.