Suppr超能文献

在接受免疫治疗的患者的回顾性数据库中识别细胞因子释放综合征和严重程度的指标。

Identification of cytokine release syndrome and indicators of severity in retrospective databases among patients receiving immunotherapy.

机构信息

Yale School of Medicine, New Haven, Connecticut, USA.

Janssen Scientific Affairs, LLC, a Johnson and Johnson Company, Horsham, Pennsylvania, USA.

出版信息

Pharmacol Res Perspect. 2024 Dec;12(6):e70024. doi: 10.1002/prp2.70024.

Abstract

Cytokine release syndrome (CRS) can occur following cancer immunotherapies, but is most often mild and of limited duration. International Classification of Diseases (ICD)-10 codes allowing identification of CRS were introduced in 2020 but may be underutilized. We evaluated the performance of a published claims-based algorithm to detect CRS (any grade) and high-grade CRS (HG, grades 2-5), as well as identified indicators of HG CRS in retrospective data. Adults with low-grade and HG CRS during an encounter coinciding with administrations of blinatumomab or chimeric antigen receptor-T therapy were identified in three types of retrospective databases (hospital chargemaster data, electronic health records, and administrative claims). The algorithm's sensitivity in detecting any CRS and HG CRS was reported. A least absolute shrinkage and selection operator (LASSO) regression model was developed to identify indicators of HG CRS. Performance of the model was evaluated using area under the curve (AUC). The sensitivity of the algorithm to detect any grade CRS ranged between 77%-100% and between 8%-80% for HG CRS, depending on the type of database. The LASSO model identified hypotension, positive pressure (including mechanical ventilation), tocilizumab, and vasopressors as indicators of HG CRS. AUC varied between 60% and 75%. The algorithm accurately detected any grade CRS for over three-quarters of instances, but was not as reliable for HG CRS. Results varied based on database attributes. Hypotension, vasopressors, positive pressure, and tocilizumab were associated with HG CRS and may be methodologically helpful signals of CRS severity in retrospective data.

摘要

细胞因子释放综合征 (CRS) 可发生于癌症免疫疗法后,但通常为轻度且持续时间有限。国际疾病分类(ICD-10)编码于 2020 年引入,可用于识别 CRS,但可能未得到充分利用。我们评估了一种已发表的基于索赔的算法,以检测 CRS(任何等级)和高级别 CRS(HG,等级 2-5)的性能,并在回顾性数据中确定了 HG CRS 的指标。在与blinatumomab 或嵌合抗原受体-T 治疗给药同时的就诊期间,在三种类型的回顾性数据库(医院计费主数据、电子健康记录和行政索赔)中识别出低级别和 HG CRS 的成年人。报告了算法检测任何 CRS 和 HG CRS 的敏感性。使用最小绝对收缩和选择算子(LASSO)回归模型来确定 HG CRS 的指标。使用曲线下面积(AUC)评估模型的性能。该算法检测任何等级 CRS 的敏感性在 77%-100%之间,HG CRS 的敏感性在 8%-80%之间,具体取决于数据库类型。LASSO 模型确定低血压、正压(包括机械通气)、托珠单抗和血管加压药为 HG CRS 的指标。AUC 在 60%至 75%之间。该算法在超过四分之三的情况下准确检测到任何等级的 CRS,但对于 HG CRS 则不太可靠。结果因数据库属性而异。低血压、血管加压药、正压和托珠单抗与 HG CRS 相关,可能是回顾性数据中 CRS 严重程度的方法学有用信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/480f/11530407/51e6e1ec1f28/PRP2-12-e70024-g002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验