CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Epidemiology and Outcomes of Hospitalized Chimeric Antigen Receptor T-Cell (CAR-T) Therapy Patients Who Developed Acute Respiratory Failure.
Epidemiology and Outcomes of Hospitalized Chimeric Antigen Receptor T-Cell (CAR-T) Therapy Patients Who Developed Acute Respiratory Failure.
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评估发生急性呼吸衰竭(ARF)的CAR-T 细胞治疗住院患者的发生率、基线特征和临床结局。研究使用 2017 至 2020 年美国全国住院患者样本(NIS)数据库。
通过国际疾病分类第十版程序编码系统(ICD-10-PCS)确定 CAR-T 治疗住院病例,并使用 ICD-10-CM 特定编码识别 ARF 患者。采用描述性统计分析基线特征、合并症、并发症和结局。
NIS 数据库显示 2017 至 2020 年共有 5,545 次 CAR-T 治疗住院,且逐年增加。高血压(39%)、血脂异常(21.7%)和静脉血栓栓塞(13%)是最常见合并症。7.1% 的住院病例报告 ARF;与未发生 ARF 的 CAR-T 住院病例相比,ARF 患者全因院内死亡率较高(32.9% 对 1.3%,P<0.001)。需要有创机械通气(IMV)的 ARF 患者,其全因院内死亡率也高于无需 IMV 者(48.9% 对 11.8%,P=0.001)。接受 CAR-T 的非霍奇金淋巴瘤、多发性骨髓瘤和白血病住院患者之间死亡率无差异。
这项迄今规模最大的研究揭示了 CAR-T 治疗住院患者发生 ARF 的比例及相关结局。伴 ARF 的 CAR-T 住院患者死亡率较高。研究强调 CAR-T 患者管理中多学科协作的重要性,并呼吁进一步明确 ARF 病因和制定有效管理策略。
Objectives: The aim of the study was to examine the incidence, baseline characteristics, and outcomes of Chimeric Antigen Receptor T-cell (CAR-T) therapy admissions in individuals who developed acute respiratory failure (ARF). The study utilized the National Inpatient Sample (NIS) database for the years 2017 to 2020. Methods: The study identified CAR-T cell therapy hospitalizations through the International Classification of Diseases, Tenth Revision, Procedure Coding System (ICD-10-PCS) codes. Patients with acute respiratory failure (ARF) were further classified using specific International Classification of Disease, Tenth Revision, Clinical Modification (ICD-10-CM) codes. Descriptive statistics were performed to analyze baseline characteristics, comorbidities, complications, and outcomes. Results: Analysis of the NIS Database identified 5545 CAR-T therapy admissions between 2017 and 2020, revealing a rising trend over time. In our study, we found that hypertension (39%), dyslipidemia (21.
7%), and venous thromboembolism (13%) were the most frequently observed comorbidities in CAR-T cell therapy admissions. Acute respiratory failure (ARF) was reported in 7. 1% of admissions, and they had higher all-cause in-hospital mortality than CAR-T cell therapy admissions without ARF (32. 9% vs 1. 3%, P < 0. 001). ARF admissions that required invasive mechanical ventilation (IMV) also had higher all-cause in-hospital mortality compared to admissions not requiring IMV (48. 9% vs 11. 8%, P = 0. 001).
There was no difference in the mortality rate among admissions with non-Hodgkin's Lymphoma, Multiple Myeloma, and Leukemia that utilized CAR-T therapy. Conclusions: In this largest study to date, we illuminate the incidence and outcomes of CAR-T cell therapy admissions with ARF.
Higher mortality rates were observed in CAR-T cell therapy admissions with ARF. The study emphasizes the crucial role of interdisciplinary collaboration in CAR-T patient management and calls for additional research to clarify ARF's etiology and inform effective management strategies.
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