English version of Japanese guidance for the use of oral Janus kinase inhibitors (JAK1 and TYK2 inhibitors) in the treatments of psoriasis

Author:

Saeki Hidehisa1ORCID,Mabuchi Tomotaka2,Asahina Akihiko3ORCID,Abe Masatoshi4,Igarashi Atsuyuki5,Imafuku Shinichi6ORCID,Okubo Yukari7ORCID,Komine Mayumi8ORCID,Takahashi Kenzo9,Torii Hideshi10ORCID,Morita Akimichi11ORCID,Yotsuyanagi Hiroshi12,Watanabe Akira13,Ohtsuki Mamitaro8,

Affiliation:

1. Department of Dermatology Nippon Medical School Tokyo Japan

2. Department of Dermatology Tokai University School of Medicine Isehara Japan

3. Department of Dermatology The Jikei University School of Medicine Tokyo Japan

4. Kojinkai Sapporo Skin Clinic Sapporo Japan

5. Department of Dermatology NTT Medical Center Tokyo Tokyo Japan

6. Department of Dermatology, Faculty of Medicine Fukuoka University Fukuoka Japan

7. Department of Dermatology Tokyo Medical University Tokyo Japan

8. Department of Dermatology Jichi Medical University Shimotsuke Japan

9. Department of Dermatology University of the Ryukyus Graduate School of Medicine Okinawa Japan

10. Division of Dermatology Tokyo Yamate Medical Center Tokyo Japan

11. Department of Geriatric and Environmental Dermatology Nagoya City University Graduate School of Medical Sciences Nagoya Japan

12. Division of Infectious Diseases Advanced Clinical Research Center Institute of Medical Science The University of Tokyo Tokyo Japan

13. Research Division for Development of Anti‐Infective Agents Faculty of Medical Science and Welfare Tohoku Bunka Gakuen University Sendai Japan

Abstract

AbstractThis is the English version of Japanese guidance for the use of oral Janus kinase (JAK) inhibitors (JAK1 and tyrosine kinase 2 [TYK2] inhibitors) in the treatments of psoriasis. Several cytokines, such as interleukin (IL)‐6, IL‐7, IL‐12, IL‐21, IL‐22, IL‐23, interferon (IFN)‐α, and IFN‐γ, are involved in the pathogenesis of psoriasis (including psoriatic arthritis). As oral JAK inhibitors hinder the JAK‐signal transducers and activators of transcription signal transduction routes involved in the signal transduction of these cytokines, they may be effective for the treatment of psoriasis. JAK has four types: JAK1, JAK2, JAK3, and TYK2. Regarding the use of oral JAK inhibitors for the treatment of psoriasis in Japan, indications of the JAK1 inhibitor upadacitinib were extended also to psoriatic arthritis in 2021, and the use of the TYK2 inhibitor deucravacitinib for plaque‐type psoriasis, pustular psoriasis, and erythrodermic psoriasis became covered by health insurance in 2022. This guidance was developed for board‐certified dermatologists who specialize in the treatment of psoriasis and to promote the proper use of oral JAK inhibitors. In the package inserts and guides for appropriate use, upadacitinib and deucravacitinib are classified as a “JAK inhibitor” and a “TYK2 inhibitor”, respectively, and it is possible that there may be differences in safety between the two drugs. The safety of these drugs will be evaluated for the future by the postmarketing surveillance for molecularly targeted drugs for psoriasis of the Japanese Dermatological Association.

Publisher

Wiley

Subject

Dermatology,General Medicine

Reference21 articles.

1. JAK/STAT pathway and nociceptive cytokine signalling in rheumatoid arthritis and psoriatic arthritis

2. In vitro and in vivo characterization of the JAK1 selectivity of upadacitinib (ABT-494)

3. TYK2 as a therapeutic target in the treatment of autoimmune and inflammatory diseases

4. AbbVieGK.Package inserts Rinvoq® (upadacitinib hydrate) tablets. (Revised May 2022). [cited 2022 November 14]. Available from:https://www.info.pmda.go.jp/go/pack/3999048G2024_1_09/(in Japanese)

5. Bristol‐Myers SquibbKK.Package inserts Sotyktu® (Deucravacitinib) tablets. (Created September 2022). [cited 2022 November 14]. Available from:https://file.bmshealthcare.jp/bmshealthcare/pdf/package/Tyk2.pdf?date=20221018(in Japanese)

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