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免疫肿瘤学副作用登记系统(SERIO)——一种用于系统分析免疫治疗诱导副作用工具

英文原题:The side effect registry immuno-oncology (SERIO) - A tool for systematic analysis of immunotherapy-induced side effects.

查看英文原题

The side effect registry immuno-oncology (SERIO) - A tool for systematic analysis of immunotherapy-induced side effects.

PubMed 2023/12/23(内容时间) Eur J Cancer Q1 · IF 7.9(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

可靠的证据基础对于罕见、复杂或治疗难治性 irAE 的决策至关重要。SERIO 有助于优化副作用管理,从而降低免疫治疗引起的发病率和死亡率。

研究思路结论见上方概要

免疫检查点抑制剂(ICI)等免疫疗法在多种肿瘤实体中有效,但会引发大量副作用。全面的真实世界分析对于识别新信号、描述诊断特征、进行风险评估、确定病理机制、评估副作用管理效果以及比较肿瘤结局至关重要。

国际在线副作用登记免疫肿瘤学(SERIO;www.serio-registry.org)收集所有肿瘤实体中罕见、复杂和严重的免疫治疗诱导的副作用,重点关注ICI诱导的免疫相关不良事件(irAE)。关系数据库管理系统(RDMS)包含关于患者和肿瘤特征、免疫治疗类型、副作用治疗以及肿瘤和irAE结局的结构化数据。数据在25个器官模块中采集,包括针对CAR-T 细胞疗法的免疫效应细胞相关神经毒性综合征(ICANS)和针对双特异性抗体的细胞因子释放综合征(CRS)的新模块。收集生物样本信息。

58 个中心来自 13 个国家,共记录了 1398 例 irAE 病例,涉及 17 种肿瘤类型。irAE 由包括 tebentafusp 和 CAR-T 细胞疗法在内的九种不同免疫疗法诱导,并导致神经系统(7.6%)、肺部(4.0%)和心脏毒性(2.9%)等。所有 irAE 中 50.0% 被分级为严重或危及生命,23.0% 的患者因类固醇难治性或类固醇依赖性 irAE 接受了二线治疗。SERIO 已贡献了 44 篇原创出版物,主题范围从 irMyocarditis 到 irEncephalitis 再到免疫治疗的长期持续后遗症。

展开英文摘要原文

Immunotherapies such as immune checkpoint inhibitors (ICI) are effective in multiple tumor entities but induce a plethora of side effects. Comprehensive real-world analyses are essential to identify new signals, characterize diagnostic features, enable risk assessment, determine pathomechanisms, assess effectiveness of side effect management and compare tumor outcomes.

The international online `Side-Effect Registry Immuno-Oncology (SERIO; www.serio-registry.org) collects rare, complex, and severe immunotherapy-induced side effects across all tumor entities with a strong focus on ICI-induced immune-related adverse events (irAE). The relational database management system (RDMS) contains structured data on patient and tumor characteristics, type of immunotherapy, treatment of side effects, and outcome of tumor and irAE. Data are captured within 25 organ modules including new modules for immune effector cell-associated neurotoxicity syndrome (ICANS) for CAR-T-cell therapies and cytokine release syndrome (CRS) for bispecific antibodies. Information on biological samples is gathered.

A total of 1398 irAE cases have been documented by 58 centers from 13 countries in patients with 17 tumor types. IrAEs were induced by nine different immunotherapies including tebentafusp and CAR-T cell therapies, and resulted, among others, in neurological (7.6%), pulmonary (4.0%), and cardiac toxicities (2.9%). 50.0% of all irAEs were graded severe or life-threatening and 23.0% of patients received second-line therapy for steroid-refractory or steroid-dependent irAE. SERIO has contributed to 44 original publications on topics ranging from irMyocarditis to irEncephalitis to long-term persistent sequelae of immunotherapy.

A reliable evidence base is crucial for decision-making in rare, complex or therapy-refractory irAE. SERIO can help optimize side effect management and thereby reduce morbidity and mortality induced by immunotherapy.

论文信息

作者
Ertl C、Ruf T、Mentzer D、Kong M、Kramer R、Bergwelt-Baildon MV、Subklewe M、Tomsitz D
第一作者单位
Department of Dermatology and Allergy, LMU University Hospital, LMU Munich, Munich, Germany; SERIO Registry (www.serio-registry.org). Electronic address: carolin.ertl@med.uni-muenchen.de.Germany
通讯作者单位
Department of Dermatology and Allergy, LMU University Hospital, LMU Munich, Munich, Germany; SERIO Registry (www.serio-registry.org); Department of Dermatology, Friedrich-Alexander University Erlangen-Nürnberg (FAU) and University Hospital Erlangen (UKER), Deutsches Zentrum Immuntherapie (DZI) and Comprehensive Cancer Center Erlangen-European Metropolitan Area of Nürnberg (CCC-ER-EMN), Erlangen, Germany. Electronic address: lucie.heinzerling@med.uni-muenchen.de.Germany
期刊
European journal of cancer (Oxford, England : 1990)2024 Mar
原文标识
PubMed 38262306 · DOI 10.1016/j.ejca.2023.113505