Evidence map›Paper›PMID 30890624›Full record

Trial reportThe oncologist2019

Adapalene Gel 0.1% Versus Placebo as Prophylaxis for Anti-Epidermal Growth Factor Receptor-Induced Acne-Like Rash: A Randomized Left-Right Comparative Evaluation (APPEARANCE).

Naoko Chayahara, Toru Mukohara, Motoko Tachihara, Yoshimi Fujishima, Atsushi Fukunaga, Ken Washio, Masatsugu Yamamoto, Kyosuke Nakata, Kazuyuki Kobayashi, Kei Takenaka and 10 more

Open access · bronzeAbstract readClinical Trial, Phase IIComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in The oncologist, 2019. 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
1.3field-weighted citation impact, top 21% 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, 13 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Recent Advances Regarding the Therapeutic Potential of Adapalene.Pharmaceuticals (Basel, Switzerland) · 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

20 authors at 3 institutions in 1 country.

Naoko ChayaharaDivision of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Toru MukoharaDivision of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan tmukohar@east.ncc.go.jp.
Motoko TachiharaDivision of Respiratory Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Yoshimi FujishimaDivision of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Atsushi FukunagaDivision of Dermatology, Department of Internal related, Kobe University Graduate School of Medicine, Kobe, Japan.
Ken WashioDivision of Dermatology, Department of Internal related, Kobe University Graduate School of Medicine, Kobe, Japan.
Masatsugu YamamotoDivision of Respiratory Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Kyosuke NakataDivision of Respiratory Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Kazuyuki KobayashiDivision of Respiratory Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Kei TakenakaDivision of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Masanori ToyodaDivision of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Naomi KiyotaDivision of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Kazutoshi TobimatsuDivision of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Hisayo DoiDepartment of Nursing, Kobe University Hospital, Kobe, Japan.
Naomi MizutaDepartment of Hospital Pharmacy, Kobe University Hospital, Kobe, Japan.
Naho MarugamiDepartment of Hospital Pharmacy, Kobe University Hospital, Kobe, Japan.
Atsushi KawaguchiEducation and Research Center for Community Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Chikako NishigoriDivision of Dermatology, Department of Internal related, Kobe University Graduate School of Medicine, Kobe, Japan.
Yoshihiro NishimuraDivision of Respiratory Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Hironobu MinamiDivision of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Kobe University · JPKobe University Hospital · JPSaga University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

lessons learnedThe results of the APPEARANCE trial indicate that adapalene does not prevent acne-like rash over placebo when added to topical moisturizer and oral minocycline but instead may have a detrimental effect. Therefore, adapalene is not recommended as prophylaxis against acne-like rash induced by anti-epidermal growth factor receptor therapies.Given that acne-like rash was completely controlled with placebo in approximately half of patients, predictive measures to identify patients needing intensive prophylaxis are required.

backgroundAnti-epidermal growth factor receptor (EGFR) therapies are frequently associated with acne-like rash. To evaluate the prophylactic efficacy of adapalene, a topical retinoid used as first-line therapy for acne vulgaris, we conducted a randomized, placebo-controlled, evaluator-blinded, left-right comparative trial.

methodsPatients with non-small cell lung, colorectal, or head and neck cancer scheduled to receive anti-EGFR therapies were randomly assigned to once-daily adapalene application on one side of the face, with placebo on the other side. All patients had topical moisturizer coapplied to both sides of the face, and received oral minocycline. The primary endpoint was the difference in total facial lesion count of acne-like rash at 4 weeks. Secondary endpoints included complete control rate (CCR) of acne-like rash (≤5 facial lesions) and global skin assessment (Investigator's Global Assessment [IGA] scale, grade 0-4) at 4 weeks. Two blinded dermatologists independently evaluated the endpoints from photographs.

resultsA total of 36 patients were enrolled, of whom 26 were evaluable. Adapalene treatment was associated with a greater lesion count than placebo at 4 weeks, although the difference was not statistically significant (mean, 12.6 vs. 9.8,

conclusionAdapalene is not recommended as prophylaxis against acne-like rash induced by anti-EGFR therapies.

Indexed as

Acne VulgarisAdapaleneAgedAged, 80 and overCarcinoma, Non-Small-Cell LungColorectal NeoplasmsDermatologic AgentsErbB ReceptorsExanthemaFemaleFollow-Up StudiesGelsHead and Neck NeoplasmsHumansLung NeoplasmsMaleAdapaleneDermatologic AgentsEGFR protein, humanErbB ReceptorsGelsProtein Kinase Inhibitors

Identifiers

PMID30890624
PMCPMC6656472
OpenAlexW2925295092

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.