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日本冷吡啉相关周期性综合征的临床特征及卡那单抗的长期真实世界疗效和耐受性:一项全国性调查结果

Clinical Characteristics of Cryopyrin-Associated Periodic Syndrome and Long-Term Real-World Efficacy and Tolerability of Canakinumab in Japan: Results of a Nationwide Survey.

作者信息

Miyamoto Takayuki, Izawa Kazushi, Masui Sho, Yamazaki Atsue, Yamasaki Yuichi, Matsubayashi Tadashi, Shiraki Mayuka, Ohnishi Hidenori, Yasumura Junko, Kawabe Tomohiro, Miyamae Takako, Matsubara Tomoyo, Arakawa Naoya, Ishige Takashi, Takizawa Takumi, Shimbo Asami, Shimizu Masaki, Kimura Naoki, Maeda Yuichi, Maruyama Yuta, Shigemura Tomonari, Furuta Junichi, Sato Satoshi, Tanaka Hiroshi, Izumikawa Miharu, Yamamura Masahiro, Hasegawa Toshio, Kaneko Hiroshi, Nakagishi Yasuo, Nakano Naoko, Iida Yasunori, Nakamura Tamaki, Wakiguchi Hiroyuki, Hoshina Takayuki, Kawai Toshinao, Murakami Kosaku, Akizuki Shuji, Morinobu Akio, Ohmura Koichiro, Eguchi Katsuhide, Sonoda Motoshi, Ishimura Masataka, Furuno Kenji, Kashiwado Momoko, Mori Masaaki, Kawahata Kimito, Hayama Koremasa, Shimoyama Kumiko, Sasaki Natsuko, Ito Taisuke, Umebayashi Hiroaki, Omori Tae, Nakamichi Seiko, Dohmoto Tomotsune, Hasegawa Yasuyuki, Kawashima Hisashi, Watanabe Shojiro, Taguchi Yuichiro, Nakaseko Haruna, Iwata Naomi, Kohno Hiroki, Ando Taiki, Ito Yasuhiko, Kataoka Yuko, Saeki Takako, Kaneko Utako, Murase Ayako, Hattori Seira, Nozawa Tomo, Nishimura Kenichi, Nakano Reiji, Watanabe Misa, Yashiro Masato, Nakamura Tomonori, Komai Toshihiko, Kato Kentaro, Honda Yoshitaka, Hiejima Eitaro, Yonezawa Atsushi, Bessho Kazuhisa, Okada Satoshi, Ohara Osamu, Takita Junko, Yasumi Takahiro, Nishikomori Ryuta

机构信息

Kyoto University, Kyoto, Japan.

Kagoshima University Hospital, Kagoshima, Japan.

出版信息

Arthritis Rheumatol. 2024 Jun;76(6):949-962. doi: 10.1002/art.42808. Epub 2024 Mar 7.

Abstract

OBJECTIVE

We assess the clinical characteristics of patients with cryopyrin-associated periodic syndrome (CAPS) in Japan and evaluate the real-world efficacy and safety of interleukin-1 (IL-1) inhibitors, primarily canakinumab.

METHODS

Clinical information was collected retrospectively, and serum concentrations of canakinumab and cytokines were analyzed.

RESULTS

A total of 101 patients were included, with 86 and 15 carrying heterozygous germline and somatic mosaic mutations, respectively. We identified 39 mutation types, and the common CAPS-associated symptoms corresponded with those in previous reports. Six patients (5.9% of all patients) died, with four of the deaths caused by CAPS-associated symptoms. Notably, 73.7% of patients (100%, 79.6%, and 44.4% of familial cold autoinflammatory syndrome, Muckle-Wells syndrome, and chronic infantile neurological cutaneous articular syndrome/neonatal onset multisystem inflammatory disease, respectively) achieved complete remission with canakinumab, and early therapeutic intervention was associated with better auditory outcomes. In some patients, canakinumab treatment stabilized the progression of epiphysial overgrowth and improved height gain, visual acuity, and renal function. However, 23.7% of patients did not achieve inflammatory remission with crucial deterioration of organ damage, with two dying while receiving high-dose canakinumab treatment. Serological analysis of canakinumab and cytokine concentrations revealed that the poor response was not related to canakinumab shortage. Four inflammatory nonremitters developed inflammatory bowel disease (IBD)-unclassified during canakinumab treatment. Dual biologic therapy with canakinumab and anti-tumor necrosis factor-α agents was effective for IBD- and CAPS-associated symptoms not resolved by canakinumab monotherapy.

CONCLUSION

This study provides one of the largest epidemiologic data sets for CAPS. Although early initiation of anti-IL-1 treatment with canakinumab is beneficial for improving disease prognosis, some patients do not achieve remission despite a high serum concentration of canakinumab. Moreover, IBD may develop in CAPS after canakinumab treatment.

摘要

目的

我们评估了日本冷吡啉相关周期性综合征(CAPS)患者的临床特征,并评价了白细胞介素-1(IL-1)抑制剂(主要是卡那单抗)在真实世界中的疗效和安全性。

方法

回顾性收集临床信息,并分析卡那单抗和细胞因子的血清浓度。

结果

共纳入101例患者,其中86例携带杂合子种系突变,15例携带体细胞镶嵌突变。我们鉴定出39种突变类型,常见的CAPS相关症状与既往报道一致。6例患者(占所有患者的5.9%)死亡,其中4例死于CAPS相关症状。值得注意的是,73.7%的患者(分别占家族性冷自身炎症综合征、穆克-韦尔斯综合征和慢性婴儿神经皮肤关节综合征/新生儿起病多系统炎症性疾病患者的100%、79.6%和44.4%)使用卡那单抗后实现完全缓解,早期治疗干预与更好的听力结果相关。在一些患者中,卡那单抗治疗稳定了骨骺过度生长的进程,并改善了身高增长、视力和肾功能。然而,23.7%的患者未实现炎症缓解,器官损害严重恶化,2例在接受高剂量卡那单抗治疗时死亡。卡那单抗和细胞因子浓度的血清学分析显示,疗效不佳与卡那单抗不足无关。4例炎症未缓解患者在卡那单抗治疗期间发生了未分类的炎症性肠病(IBD)。卡那单抗与抗肿瘤坏死因子-α药物联合生物治疗对卡那单抗单药治疗未解决的IBD和CAPS相关症状有效。

结论

本研究提供了最大的CAPS流行病学数据集之一。尽管早期使用卡那单抗启动抗IL-1治疗有利于改善疾病预后,但一些患者尽管血清卡那单抗浓度较高仍未实现缓解。此外,CAPS患者在卡那单抗治疗后可能发生IBD。

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