Evidence map›Paper›PMID 22472354›Full record

ArticleEuropean journal of medical research2012

Management of EGFR-inhibitor associated rash: a retrospective study in 49 patients.

Peter Arne Gerber, Stephan Meller, Tatiana Eames, Bettina Alexandra Buhren, Holger Schrumpf, Sonja Hetzer, Laura Maximiliane Ehmann, Wilfried Budach, Edwin Bölke, Christiane Matuschek and 2 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in European journal of medical research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04864717 (A Randomized Control Trial to Compare Doxycycline to Isotretinoin for the Treatment of Acneiform Eruptions in Cancer Patients on Tyrosine Kinase Inhibitors), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 22% 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.

NCT04864717 phase4unknown statusnot on this mapstarted 2021, after this paper: background citation

A Randomized Control Trial to Compare Doxycycline to Isotretinoin for the Treatment of Acneiform Eruptions in Cancer Patients on Tyrosine Kinase Inhibitors

TypeinterventionalSponsorLady Davis InstituteRan2021 to 2022Enrolled98ConditionsAcneiform Eruptions, Cancer, Treatment-RelatedArmsDoxycycline 100mg po once daily x 6 months, Isotretinoin 40 mg po once daily x 6 months
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. [Cutaneous side effects of targeted cancer drugs].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2017
    Review
  6. [Drug reactions caused by chemotherapy agents].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2014
    Review
  7. Updated Physician's Guide to the Off-label Uses of Oral Isotretinoin.The Journal of clinical and aesthetic dermatology · 2014
    Review
  8. Review
  9. 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

12 authors at 2 institutions in 1 country.

Peter Arne GerberDepartment of Dermatology, University of Duesseldorf, Medical Faculty, Moorenstrasse 5, D-40225 Duesseldorf, Germany. peterarne.gerber@uni-duesseldorf.de
Stephan Meller
Tatiana Eames
Bettina Alexandra Buhren
Holger Schrumpf
Sonja Hetzer
Laura Maximiliane Ehmann
Wilfried Budach
Edwin Bölke
Christiane Matuschek
Andreas Wollenberg
Bernhard Homey
Heinrich Heine University Düsseldorf · DELudwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn recent years inhibitors directed against the epidermal growth factor receptor (EGFR) have evolved as effective targeting cancer drugs. Characteristic papulopustular exanthemas, often described as acneiform rashes, are the most frequent adverse effect associated with this class of novel cancer drugs and develop in > 90% of patients. Notably, the rash may significantly compromise the patients' quality of life, thereby potentially leading to incompliance as well as dose reduction or even termination of the anti-EGFR therapy. Yet, an effective dermatologic management of cutaneous adverse effects can be achieved. Whereas various case reports, case series or expert opinions on the management of EGFR-inhibitor (EGFRI) induced rashes have been published, data on systematic management studies are sparse.

methodsHere, we present a retrospective, uncontrolled, comparative study in 49 patients on three established regimens for the management of EGFRI-associated rashes.

resultsStrikingly, patients' rash severity improved significantly over three weeks of treatment with topical mometason furoate cream, topical prednicarbate cream plus nadifloxacin cream, as well as topical prednicarbate cream plus nadifloxacin cream plus systemic isotretinoin.

conclusionsIn summary our results demonstrate that EGFRI-associated rashes can be effectively managed by specific dermatologic interventions. Whereas mild to moderate rashes should be treated with basic measures in combination with topical glucocorticosteroids or combined regiments using glucocorticosteroids and antiseptics/antibiotics, more severe or therapy-resistant rashes are likely to respond with the addition of systemic retinoids.

Indexed as

ExanthemaProtein Kinase InhibitorsAdministration, TopicalErbB ReceptorsFluoroquinolonesHumansIsotretinoinMometasone FuroatePregnadienediolsQuinolizinesEGFR protein, humanErbB ReceptorsFluoroquinolonesIsotretinoinMometasone FuroatenadifloxacinPregnadienediolsProtein Kinase InhibitorsQuinolizines

Identifiers

PMID22472354
PMCPMC3351712
OpenAlexW2141659290

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.