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SATISFY-JP,一项关于抗白细胞介素-6受体抗体萨特利珠单抗用于治疗具有免疫反应表型的肺动脉高压患者的II期多中心开放标签研究:研究方案。

SATISFY-JP, a phase II multicenter open-label study on Satralizumab, an anti-IL-6 receptor antibody, use for the treatment of pulmonary arterial hypertension in patients with an immune-responsive-phenotype: Study protocol.

作者信息

Tamura Yuichi, Takeyasu Rika, Takata Tomohiro, Miyazaki Naoki, Takemura Ryo, Wada Michihiko, Tamura Yudai, Abe Kohtaro, Shigeta Ayako, Taniguchi Yu, Adachi Shiro, Inami Takumi, Tsujino Ichizo, Tahara Nobuhiro, Kuwana Masataka

机构信息

Pulmonary Hypertension Center International University of Health and Welfare Mita Hospital Tokyo Japan.

Department of Cardiology International University of Health and Welfare School of Medicine Narita Japan.

出版信息

Pulm Circ. 2023 Jun 19;13(2):e12251. doi: 10.1002/pul2.12251. eCollection 2023 Apr.

Abstract

Pulmonary arterial hypertension (PAH), an intractable disease with a poor prognosis, is commonly treated using pulmonary vasodilators modulating the endothelin, cGMP, and prostacyclin pathway. Since the 2010s, drugs for treating pulmonary hypertension based on mechanisms other than pulmonary vasodilation have been actively developed. However, precision medicine is based on tailoring disease treatment to particular phenotypes by molecular-targeted drugs. Since interleukin-6 (IL-6) is involved in the development of PAH in animal models, and some patients with PAH have elevated IL-6 levels, the cytokine is expected to obtain potentials for therapeutic targeting. Accordingly, we identified a phenotype with elevated cytokine activity of the IL-6 family in the PAH population by combining case data extracted from the Japan Pulmonary Hypertension Registry with a comprehensive analysis of 48 cytokines using artificial intelligence clustering techniques. Including an IL-6 threshold ≥2.73 pg/mL as inclusion criteria for reducing the risk of insufficient efficacy, an investigator-initiated clinical study using satralizumab, a recycling anti-IL6 receptor monoclonal antibody, for patients with an immune-responsive phenotype is underway. This study is intended to test whether use of patient biomarker profile can identify a phenotype responsive to anti-IL6 therapy.

摘要

肺动脉高压(PAH)是一种预后较差的难治性疾病,通常使用调节内皮素、环磷酸鸟苷(cGMP)和前列环素途径的肺血管扩张剂进行治疗。自2010年代以来,基于肺血管扩张以外机制的肺动脉高压治疗药物得到了积极开发。然而,精准医学是基于通过分子靶向药物针对特定表型定制疾病治疗。由于白细胞介素-6(IL-6)参与动物模型中PAH的发展,并且一些PAH患者的IL-6水平升高,因此这种细胞因子有望成为治疗靶点。因此,我们通过将从日本肺动脉高压登记处提取的病例数据与使用人工智能聚类技术对48种细胞因子进行的综合分析相结合,在PAH人群中确定了IL-6家族细胞因子活性升高的表型。以IL-6阈值≥2.73 pg/mL作为降低疗效不足风险的纳入标准,一项由研究者发起的针对具有免疫反应性表型患者的使用抗IL-6受体单克隆抗体萨特利珠单抗的临床研究正在进行。本研究旨在测试使用患者生物标志物谱是否可以识别对抗IL-6治疗有反应的表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a152/10278205/b45b557779f0/PUL2-13-e12251-g002.jpg

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