TY - JOUR
T1 - A multicenter, open-label, uncontrolled, single-arm phase 2 study of tirabrutinib, an oral Bruton's tyrosine kinase inhibitor, in pemphigus
AU - Yamagami, Jun
AU - Ujiie, Hideyuki
AU - Aoyama, Yumi
AU - Ishii, Norito
AU - Tateishi, Chiharu
AU - Ishiko, Akira
AU - Ichijima, Tomoki
AU - Hagihara, Shunsuke
AU - Hashimoto, Koji
AU - Amagai, Masayuki
N1 - Funding Information:
Jun Yamagami has received research funding, consultancy fees, lecture fees, and travel expenses from Ono Pharmaceutical Co., Ltd. for this study; and lecture and consultancy fees from Ono Pharmaceutical Co., Ltd., lecture fees from Japan Blood Products Organization and Nihon Pharmaceutical Co., Ltd., and a research grant from Japan Agency for Medical Research and Development (AMED Practical Research Project for Rare / Intractable Diseases) outside the submitted work. Hideyuki Ujiie has received research funding and travel expenses from Ono Pharmaceutical Co., Ltd. for this study; and research grants from Novartis Japan, Takeda Science Foundation, Bristol-Myers Squibb, Kobayashi Foundation, and Torii Pharmaceutical Co., Ltd.; research grants and personal fees (lecture fees) from Mitsubishi Tanabe Pharma and Maruho Co., Ltd.; and personal fees (lecture fees) from Ono Pharmaceutical Co., Ltd., Japan Blood Products Organization, Taiho Pharmaceutical Co., Ltd., Kyowa Kirin Co., Ltd., Kowa Pharmaceutical Co., Ltd., Sanofi S.A., Medical & Biological Laboratories Co., Ltd., Daiichi Sankyo Co., Ltd., and Nihon Pharmaceutical Co., Ltd. outside the submitted work. Yumi Aoyama has received research funding, consultancy fees, and travel expenses from Ono Pharmaceutical Co., Ltd. for this study; and research funding from Kanebo Cosmetics and Maruho Co., Ltd. outside the submitted work. Norito Ishii has received research funding, consultancy fees, and travel expenses from Ono Pharmaceutical Co., Ltd. for this study. Chiharu Tateishi has received research funding and travel expenses from Ono Pharmaceutical Co., Ltd. for this study; and grants and personal fees from Maruho Co., Ltd., Novartis Pharma K.K., Mitsubishi Tanabe Pharma Corporation, Eisai Co., Ltd., Celgene Corporation, Taiho Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Sanofi K.K., AbbVie G.K., Kyowa Kirin Co., Ltd., Jimro Co., Ltd., Minophagen Pharmaceutical Co., Ltd., and Sun Pharma Japan Ltd.; grants from Pfizer Japan Inc., Boehringer Ingelheim International GmbH, UCB Japan Co. Ltd., Bristol-Myers Squibb Company, Pfizer R&D Japan G.K., Nippon Kayaku Co., Ltd., Tsumura Co., Ltd., Kotaro Pharmaceutical Co., Ltd., Torii Pharmaceutical Co., Ltd., Pola Pharma Co., Ltd., Taisho Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd., Smith & Nephew K.K., Nihon Pharmaceutical Co., Ltd., Ezaki Glico Co., Ltd., Nippon Zoki Pharmaceutical Co., Ltd., Otsuka Pharmaceutical Co., Ltd., MSD K.K., EA Pharma Co., Ltd., Kyowa CritiCare Co., Ltd., Kaken Pharmaceutical Co., Ltd., Teijin Pharma Limited, Nippon Shokubai Co., Ltd., Nobelpharma Co., Ltd., SBI Pharmaceuticals Co., Ltd., Kao Corporation, Tokiwa Pharmaceutical Co., Ltd., Amgen K.K., and Parexel International Inc.; and personal fees from Janssen Pharmaceutical K.K., Medical & Biological Laboratories Co., Ltd., LEO Pharma K.K., and Chugai Pharmaceutical Co., Ltd. outside the submitted work. Akira Ishiko has received research funding and travel expenses from Ono Pharmaceutical Co., Ltd. for this study; and research funding from Sato Yakuhin Kogyo Co., Ltd., Sun Pharmaceutical Industries Ltd., Novartis Japan, Pfizer Japan Inc., and Shiseido Co., Ltd.; research funding and personal fees (lecture fees) from Taiho Pharmaceutical Co., Ltd., Torii Pharmaceutical Co., Ltd., Kaken Pharmaceutical Co., Ltd., Maruho Co., Ltd., Kyowa Kirin Co., Ltd., Mitsubishi Tanabe Pharma, and Nihon Pharmaceutical Co., Ltd.; research funding and personal fees (advisory fees) from Ishin Pharma; and personal fees (advisory fees) from Kao Co., Ltd. outside the submitted work. Tomoki Ichijima and Shunsuke Hagihara are employees of Ono Pharmaceutical Co., Ltd. Koji Hashimoto has received consultancy fees and travel expenses from Ono Pharmaceutical Co., Ltd. for this study; and personal fees (consultancy and lecture fees) from Maruho Co., Ltd., personal fees (lecture fees) from Sunstar Inc., and non-financial support (travel expenses) from Kyowa Kirin Co., Ltd. outside the submitted work. Masayuki Amagai has received research funding, consultancy fees, and travel expenses from Ono Pharmaceutical Co., Ltd. for this study; and a research grant from Japan Agency for Medical Research and Development (AMED Practical Research Project for Rare / Intractable Diseases) and research funding from Medical & Biological Laboratories Co., Ltd. outside the submitted work; and has a patent (US 7550562 B2) for a pemphigus monoclonal antibody licensed to Keio University.
Publisher Copyright:
© 2021 The Authors
PY - 2021/9
Y1 - 2021/9
N2 - Background: The treatment of pemphigus is based on systemic corticosteroid use and adjuvant therapies, but some patients are resistant to conventional therapy. Tirabrutinib is a highly selective oral Bruton's tyrosine kinase inhibitor that may be clinically effective in treating pemphigus by suppressing B-cell signaling. Objective: We investigated the efficacy and safety of tirabrutinib in patients with refractory pemphigus. Methods: This was a multicenter, open-label, single-arm phase 2 study of Japanese patients with refractory pemphigus receiving appropriate treatment with an oral corticosteroid and adjuvant therapies. Patients received postprandial oral tirabrutinib 80 mg once daily for 52 weeks. After 16 weeks of tirabrutinib treatment, the corticosteroid dose was tapered to ≤10 mg/day of prednisolone equivalent. Results: In total, 16 patients were evaluated (mean age, 52.5 years; 50 % male). The complete remission rate after 24 weeks of treatment (primary endpoint) was 18.8 % (3/16; 95 % confidence interval, 6.6 %–43.0 %). By Week 52, eight patients (50.0 %) achieved complete remission and 10 patients (62.5 %) achieved remission. Over 52 weeks of treatment, the mean prednisolone dose decreased from 17.03 to 7.65 mg/day. Incidences of adverse events (AEs) and adverse drug reactions were 87.5 % and 43.8 %, respectively. A relationship with tirabrutinib was ruled out for all serious AEs and Grade ≥3 AEs. Conclusion: Treatment with tirabrutinib enabled remission and reduced oral corticosteroid exposure over time and did not result in any major safety concerns in patients with refractory pemphigus. Thus, oral tirabrutinib may be a new treatment option for patients with refractory pemphigus.
AB - Background: The treatment of pemphigus is based on systemic corticosteroid use and adjuvant therapies, but some patients are resistant to conventional therapy. Tirabrutinib is a highly selective oral Bruton's tyrosine kinase inhibitor that may be clinically effective in treating pemphigus by suppressing B-cell signaling. Objective: We investigated the efficacy and safety of tirabrutinib in patients with refractory pemphigus. Methods: This was a multicenter, open-label, single-arm phase 2 study of Japanese patients with refractory pemphigus receiving appropriate treatment with an oral corticosteroid and adjuvant therapies. Patients received postprandial oral tirabrutinib 80 mg once daily for 52 weeks. After 16 weeks of tirabrutinib treatment, the corticosteroid dose was tapered to ≤10 mg/day of prednisolone equivalent. Results: In total, 16 patients were evaluated (mean age, 52.5 years; 50 % male). The complete remission rate after 24 weeks of treatment (primary endpoint) was 18.8 % (3/16; 95 % confidence interval, 6.6 %–43.0 %). By Week 52, eight patients (50.0 %) achieved complete remission and 10 patients (62.5 %) achieved remission. Over 52 weeks of treatment, the mean prednisolone dose decreased from 17.03 to 7.65 mg/day. Incidences of adverse events (AEs) and adverse drug reactions were 87.5 % and 43.8 %, respectively. A relationship with tirabrutinib was ruled out for all serious AEs and Grade ≥3 AEs. Conclusion: Treatment with tirabrutinib enabled remission and reduced oral corticosteroid exposure over time and did not result in any major safety concerns in patients with refractory pemphigus. Thus, oral tirabrutinib may be a new treatment option for patients with refractory pemphigus.
KW - Efficacy
KW - Japan
KW - Phase 2 study
KW - Refractory pemphigus
KW - Safety
KW - Tirabrutinib
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UR - http://www.scopus.com/inward/citedby.url?scp=85112056800&partnerID=8YFLogxK
U2 - 10.1016/j.jdermsci.2021.07.002
DO - 10.1016/j.jdermsci.2021.07.002
M3 - Article
C2 - 34376340
AN - SCOPUS:85112056800
SN - 0923-1811
VL - 103
SP - 135
EP - 142
JO - Journal of Dermatological Science
JF - Journal of Dermatological Science
IS - 3
ER -