Volume 48, Issue 8 pp. 1262-1267
CONCISE COMMUNICATION

Follicular extension of atypical keratinocytes predicts the resistance of actinic keratosis to topical imiquimod treatment: A single-center retrospective analysis

Ryo Tanaka

Corresponding Author

Ryo Tanaka

Department of Dermatology, Hiratsuka City Hospital, Hiratsuka, Japan

Department of Dermatology, Keio University School of Medicine, Tokyo, Japan

Correspondence

Ryo Tanaka, Department of Dermatology, Hiratsuka City Hospital, 1-19-1 Minamihara, Hiratsuka-shi, Kanagawa 254-0065, Japan.

Email: [email protected]

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Keiji Tanese

Keiji Tanese

Department of Dermatology, Keio University School of Medicine, Tokyo, Japan

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Yingyao Zhu

Yingyao Zhu

Department of Dermatology, Hiratsuka City Hospital, Hiratsuka, Japan

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Yumi Fujio

Yumi Fujio

Department of Dermatology, Hiratsuka City Hospital, Hiratsuka, Japan

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Izumi Konohana

Izumi Konohana

Department of Dermatology, Hiratsuka City Hospital, Hiratsuka, Japan

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Yuichi Kurihara

Yuichi Kurihara

Department of Dermatology, Hiratsuka City Hospital, Hiratsuka, Japan

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First published: 25 April 2021
Citations: 1

Abstract

Topical imiquimod therapy has been widely used for actinic keratosis (AK). However, some cases are refractory to treatment. Therefore, an indicator that can predict its efficacy is desired. Herein, we retrospectively analyzed 52 AK lesions treated with imiquimod to investigate the characteristics of refractory lesions. Imiquimod was applied in a cycle of three times weekly for 4 weeks, followed by a 4-week break. This treatment cycle was repeated up to three times and treatment responses were evaluated. As a result, a complete response (CR) was observed in 78.8% (41/52) of lesions. Next, treatment response of lesions was correlated with clinicopathological characteristics including clinical morphology and thickness, pathological morphology and thickness, and presence of follicular extension (FE). Of these, lesions with FE were significantly less responsive to imiquimod treatment; while 92.6% of AK lesions without FE achieved a CR, only 64.0% of AK lesions with FE achieved a CR (p = 0.029). Logistic regression analysis revealed that FE was the sole significant predictor of its efficacy (p = 0.019). These results suggest that preliminary histological evaluation of FE may be useful to predict the efficacy of imiquimod for AK.

CONFLICT OF INTEREST

None declared.

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