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Abstract Number: 0520

Disease Duration Differentially Affects the Clinical Efficacy of Biologics and JAK Inhibitors in Rheumatoid Arthritis: The ANSWER Cohort Study

Yoichi Nakayama1, Daijiro Kabata2, Wataru Yamamoto3, Hidehiko Makino4, Koji Nagai4, Naofumi Yoshida5, Yonsu Son5, Masaki Katayama6, Hirotaka Yamada7, Keisuke Nishimura7, Ryota Hara8, Ryu Watanabe9, Yuki Etani10, Kosuke Ebina11, Hideo Onizawa12, Takayuki Fujii13, Akira Onishi14, Kosaku Murakami15, Koichi Murata12, Masao Tanaka14, Shuichi Matsuda12, Akio Morinobu16, Ayumi Shintani2 and Motomu Hashimoto9, 1Department of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Hirakata-shi, Osaka-fu, Japan, 2Department of Medical Statistics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan, 3Department of Health Information Management, Kurashiki Sweet Hospital, Kurashiki, Okayama, Japan, 4Department of Internal Medicine (IV), Osaka Medical and Pharmaceutical University, Osaka, Japan, 5First Department of Internal Medicine, Kansai Medical University, Hirakata, Osaka, Japan, 6Department of Rheumatology, Osaka Red Cross Hospital, Osaka, Japan, 7Department of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan, 8Department of Orthopaedic Surgery, Nara Medical University, Nara, Nara, Japan, 9Department of Clinical Immunology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan, 10Department of Sports Medical Biomechanics, Osaka University Graduate School of Medicine, Suita, Osaka, Japan, 11Department of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Suita, Osaka, Japan, 12Department of Advanced Medicine for Rheumatic Diseases, Kyoto University Graduate School of Medicine, Kyoto, Kyoto, Japan, 13Kyoto University, Kyoto, Japan, 14Department of Advanced Medicine for Rheumatic Diseases, Kyoto University Graduate School of Medicine, Kyoto, Japan, 15Division of Clinical Immunology and Cancer Immunotherapy, Center for Cancer Immunotherapy and Immunobiology, Graduate School of Medicine, Kyoto University, Kyoto, Kyoto, Japan, 16Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan., Kyoto, Japan

Meeting: ACR Convergence 2024

Keywords: Cohort Study, Disease-Modifying Antirheumatic Drugs (Dmards), rheumatoid arthritis

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Session Information

Date: Saturday, November 16, 2024

Title: RA – Treatment Poster I

Session Type: Poster Session A

Session Time: 10:30AM-12:30PM

Background/Purpose: A delay in initiating disease-modifying antirheumatic drugs (DMARDs) has been linked to poor outcomes in patients with rheumatoid arthritis (RA). Several studies have implicated the association between disease duration of RA and treatment responses of DMARDs. However, few studies have elucidated the association between disease duration and clinical efficacy of biological disease-modifying antirheumatic drugs (bDMARDs) and Janus kinase inhibitors (JAKi). In this study, we compared the changes of disease activity scores about bDMARDs and JAKi depending on different disease duration in b/ts-DMARDs naïve patients in the real-world setting.

Methods: This was a retrospective cohort study using the Kansai Consortium for Well-being of Rheumatic Disease Patients (ANSWER) cohort, a multicenter observational registry of patients with RA in Japan. bDMARDs or JAKi-naïve patients with RA who were started bDMARDs or JAKi were recruited. Patients were stratified based on disease duration (Early, ≤ 1 year; Late, >1 year). Mean change ratios of clinical disease activity index (CDAI) and Health Assessment Questionnaire Disease Index (HAQ-DI) from Day 0 to Day 365 (Day 365/Day 0) after the initiation of bDMARDs or JAKi calculated by the generalized estimating equations were compared between the Early and the Late group.

Results: A total of 2,344 patients with RA were enrolled. The median disease duration at the initiation of bDMARDs of the Early group was 0.5 years and the Late group was 3.6 years. The median disease duration at the initiation of JAKi of the Early group was 0.5 years and the Late group was 5.7 years. In bDMARDs-treated group, mean change ratios (Day 365/Day 0) of CDAI were 0.15 (95%CI 0.13-0.19) in the Early group and 0.25 (95%CI 0.21-0.29) in the Late group (p< 0.001) (Figure 1A). In contrast, in JAKi-treated group, mean change ratios (Day 365/Day 0) of CDAI were 0.27 (95%CI 0.12-0.58) in the Early group and 0.17 (95%CI 0.10-0.28) in the Late group (p=0.09) (Figure 1B). In bDMARDs, mean change ratios (Day 365/Day 0) of HAQ-DI were 0.29 (95%CI 0.24-0.36) in the Early group and 0.56 (95%CI 0.48-0.65) in the Late group (p< 0.001) (Figure 2A). In JAKi, mean change ratios (Day 365/Day 0) of CDAI were 0.32 (95%CI 0.18-0.59) in the Early group and 0.41 (95%CI 0.27-0.60) in the Late group (p=0.71) (Figure 2B).

Conclusion: bDMARDs were more effective in patients with shorter disease duration, while JAKi were effective irrespective of disease duration. The initiation of bDMARDs should be performed as early as possible in patients with shorter disease duration, and in patients with longer disease duration, JAKi can be a good treatment option.

Supporting image 1

Figure 1. The non-linear estimated regression lines of clinical disease activity index (CDAI) after the initiation of biological disease-modifying antirheumatic drugs (bDMARDs) and Janus kinase inhibitors (JAKi). (A) bDMARDs, (B) JAKi.

Supporting image 2

Figure 2. The non-linear estimated regression lines of health assessment questionnaire disease index (HAQ-DI) after the initiation of biological disease-modifying antirheumatic drugs (bDMARDs) and Janus kinase inhibitors (JAKi). (A) bDMARDs, (B) JAKi.


Disclosures: Y. Nakayama: None; D. Kabata: None; W. Yamamoto: None; H. Makino: None; K. Nagai: None; N. Yoshida: None; Y. Son: None; M. Katayama: None; H. Yamada: None; K. Nishimura: None; R. Hara: AbbVie/Abbott, 6, Asahi-Kasei, 6, Eisai, 6, Eli Lilly, 6; R. Watanabe: AbbVie/Abbott, 5, Eli Lilly, 6, GlaxoSmithKlein(GSK), 6, UCB, 6; Y. Etani: Asahikasei, 5, Taisho, 5; K. Ebina: AbbVie/Abbott, 6, Amgen, 6, Asahi Kasei, 1, 6, Astellas, 6, Chugai, 6, Eisai, 6, Eli Lilly, 6, Ono, 6, Pfizer, 6, Taisho, 1, 6, Teijin Pharma, 1, 6, UCB, 6; H. Onizawa: None; T. Fujii: None; A. Onishi: AbbVie/Abbott, 6, Eli Lilly, 6, Pfizer, 5, 6, UCB, 6; K. Murakami: None; K. Murata: Asahi kasei Phama, 6, 12, Endowed Chairs, Ayumi Phama, 12, Endowed Chairs, Daiichi-Sankyo, 6, Mitsubishi-Tanabe Pham, 6; M. Tanaka: AbbVie/Abbott, 1, 6, Asahi Kasei Pharma Corp., 12, My course receives donations, Astellas Pharma Inc., 1, 6, Ayumi Pharmaceutical Corp., 12, My course receives donations, Bristol-Myers Squibb(BMS), 1, Chugai Pharmaceutical Co., Ltd., 6, Daiichi Sankyo Co. Ltd., 1, 6, Eisai Co., Ltd., 1, 6, Nippon Zoki Pharmaceutical Co., Ltd., 1, Pfizer Inc., 6, Taisho Pharmaceutical Co., Ltd., 1, 6, UCB Japan Co., Ltd., 1, 6; S. Matsuda: Asahi Kasei, 6, AUSPICIOUS, 6, Ayumi, 6, Chugai, 6, Daiichi Sankyo, 6, Ethicon, 6, Hisamitsu, 6, Japan Sigmax, 6, JTEC, 6, Kirin, 6, Kyocera, 2, 5, 6, Medacta, 6, Nihon Zoki, 6, Olympus, 6, Pfizer, 6, Smith and Nephew, 6, Stryker, 6, Taisho, 6, Tanabe Mitsubishi, 6, Teijin, 6, Zimmer-Biomet, 5, 6; A. Morinobu: None; A. Shintani: None; M. Hashimoto: Asahi Kasei Pharma, 5, Astellas, 5, Bristol-Myers Squibb(BMS), 5, Eli Lilly, 5, Taisho Toyama, 5.

To cite this abstract in AMA style:

Nakayama Y, Kabata D, Yamamoto W, Makino H, Nagai K, Yoshida N, Son Y, Katayama M, Yamada H, Nishimura K, Hara R, Watanabe R, Etani Y, Ebina K, Onizawa H, Fujii T, Onishi A, Murakami K, Murata K, Tanaka M, Matsuda S, Morinobu A, Shintani A, Hashimoto M. Disease Duration Differentially Affects the Clinical Efficacy of Biologics and JAK Inhibitors in Rheumatoid Arthritis: The ANSWER Cohort Study [abstract]. Arthritis Rheumatol. 2024; 76 (suppl 9). https://acrabstracts.org/abstract/disease-duration-differentially-affects-the-clinical-efficacy-of-biologics-and-jak-inhibitors-in-rheumatoid-arthritis-the-answer-cohort-study/. Accessed .
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