Evidence map›Paper›PMID 40503645›Full record

Trial reportThe Journal of dermatology2025

Facial Skin With Conspicuous Enlarged Pores Closely Related to Severity of Facial Acneiform Rash and Therapeutic Effects of EGFR Inhibitors in RAS Wild-Type Metastatic Colorectal Cancer: Ancillary Analysis of FAEISS Study (NCCH1512).

Shusuke Yoshikawa, Katsuko Kikuchi, Keiko Nozawa, Yasuko Nakai, Haruhiko Fukuda, Taro Shibata, Ryunosuke Machida, Tetsuya Hamaguchi, Atsuo Takashima, Sumiko Takatsuka and 8 more

Abstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in The Journal of dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Shusuke YoshikawaDermatology Division, Shizuoka Cancer Center Hospital, Shizuoka, Japan.ORCID https://orcid.org/0009-0002-6082-4696
Katsuko KikuchiSendai Taihaku Dermatology Clinic, Sendai, Japan.
Keiko NozawaDepartment of Nursing, Faculty of Nursing, Mejiro University Faculty of Nursing, Iwatsuki, Japan.
Yasuko NakaiNakai Dermatology Clinic, Tsu, Japan.
Haruhiko FukudaClinical Research Support Office, National Cancer Center Hospital, Tokyo, Japan.
Taro ShibataClinical Research Support Office, National Cancer Center Hospital, Tokyo, Japan.
Ryunosuke MachidaClinical Research Support Office, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-3734-6203
Tetsuya HamaguchiDepartment of Medical Oncology, Saitama Medical University International Medical Center, Saitama, Japan.
Atsuo TakashimaDepartment of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Sumiko TakatsukaDepartment of Dermatology, Niigata Cancer Center Hospital, Niigata, Japan.
Tomohiro NishinaDepartment of Gastrointestinal Medical Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama, Japan.
Akihito KawazoeDepartment of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Takahiro TsushimaDivision of Gastrointestinal Oncology, Shizuoka Cancer Center Hospital, Shizuoka, Japan.ORCID https://orcid.org/0000-0003-3551-7504
Masanobu TakahashiDepartment of Medical Oncology, Tohoku University Hospital, Sendai, Japan.
Akiko HasegawaDepartment of Medical Oncolog, Osaka International Cancer Institute, Osaka, Japan.
Toshiki MasuishiDepartment of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.ORCID https://orcid.org/0000-0002-7521-1596
Naoya YamazakiDepartment of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-9638-0428
Yoshio KiyoharaDermatology Division, Shizuoka Cancer Center Hospital, Shizuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prophylactic treatment with oral minocycline or doxycycline, moisturizers, and sunscreens has been reported to be beneficial for acneiform rash (AfR) caused by epidermal growth factor receptor (EGFR) inhibitors. It is desirable to predict which patients may develop severe AfR and provide prophylactic treatment. This study aimed to evaluate the association between the worst grade of facial AfR (FAfR) after initiating therapy with EGFR inhibitors and the characteristic skin type in patients with RAS wild-type metastatic colorectal cancer enrolled in the FAEISS study (a phase III, open-label, randomized trial evaluating topical corticosteroids for Facial Acneiform dermatitis by EGFR Inhibitors: Stepwise rank down from potent corticosteroids). Using pretreatment photographs of the face, characteristic skin types, including enlarged pores, oiliness (greasiness), and skin color/redness, were graded on a scale of 1-3. Grade 2 or higher FAfR developed in 9.1%, 27.0%, and 45.8% of patients with enlarged pore scores of 1, 2, and 3, respectively. Patients with enlarged pores tended to have more severe FAfR (p = 0.0216). Moreover, the disease control rate (complete remission/partial remission/stable disease) of the primary disease was seen in 59.1%, 70.6%, and 87.0% of patients with an enlarged pore score of 1, 2, and 3, respectively, showing a statistically significant trend (p = 0.038). This study suggests that a facial skin type with a high number of enlarged pores may be a marker for predicting AfR risk due to anti-EGFR antibody therapy and better therapeutic effects for RAS wild-type metastatic colorectal cancer.

Indexed as

Acneiform EruptionsColorectal NeoplasmsFacial DermatosesProtein Kinase InhibitorsAdultAgedCetuximabErbB ReceptorsFaceFemaleHumansMaleMiddle AgedSeverity of Illness IndexSkinTreatment OutcomeCetuximabEGFR protein, humanErbB ReceptorsProtein Kinase Inhibitorsacneiform rashcolorectal cancerenlarged poresepidermal growth factor receptor (EGFR)facial skin type

Identifiers

PMID40503645
PMCPMC12315636

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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.