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:Disseminated intravascular coagulation in chimeric antigen receptor T-cell therapy: a 6-year nationwide analysis of clinical outcomes and health care resource utilization in patients with hematologic malignancies.
Disseminated intravascular coagulation in chimeric antigen receptor T-cell therapy: a 6-year nationwide analysis of clinical outcomes and health care resource utilization in patients with hematologic malignancies.
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。
DIC 是 CAR-T 细胞治疗中不常见但严重的并发症,与死亡率升高、器官功能障碍、重症监护使用、输血需求、住院时间延长及费用增加相关。这些发现凸显了临床警惕和早期干预策略的重要性。
弥散性血管内凝血(DIC)是嵌合抗原受体(CAR)T细胞疗法公认的并发症,并导致治疗相关发病率与死亡率。然而,关于其临床和经济影响的数据仍然有限。
本研究利用美国全国性数据,探讨了接受 CAR-T 细胞治疗的血液系统恶性肿瘤住院患者中与 DIC 相关的特征和结局。
2017-2022年因急性淋巴细胞白血病、非霍奇金淋巴瘤或多发性骨髓瘤接受CAR-T 细胞治疗的成人住院患者,从全国住院患者样本中识别。住院患者按DIC状态分层,并进行调查加权分析以生成全国估计值。采用多变量回归评估死亡率和其他结局的差异(P < .05)。
在10,450例加权CAR-T 细胞治疗住院病例中,220例(2.1%)发生DIC。发生DIC的住院病例院内死亡率显著更高(22.7% vs 2.4%;校正比值比[aOR],10.96;95%置信区间[CI],4.78-25.09)。DIC与急性肾损伤(aOR,6.01)、呼吸衰竭(aOR,9.96)和休克(aOR,18.55)的更高风险相关,并与肾脏替代治疗、机械通气和血管升压药的使用增加相关。DIC还与胃肠道出血的更高风险(aOR,12.41)和更高的输血需求相关。DIC与更长的住院时间(= +17.6天;P < .001)和更高的住院费用(= +$523,323;P = .02)相关。
Disseminated intravascular coagulation (DIC) is a recognized complication of chimeric antigen receptor (CAR) T-cell therapy and contributes to treatment-related morbidity and mortality. However, data on its clinical and financial impact remain limited.
This study examined the characteristics and outcomes associated with DIC among hospitalizations for hematologic malignancies undergoing CAR-T cell therapy using national U.S. data.
Adult hospitalizations with acute lymphoblastic leukemia, non-Hodgkin lymphoma, or multiple myeloma who received CAR T-cell therapy (2017-2022) were identified from the National Inpatient Sample. Hospitalizations were stratified by DIC status, and survey-weighted analyses were performed to generate national estimates. Multivariable regression was used to assess differences in mortality and other outcomes ( P < .05).
Among 10,450 weighted CAR T-cell therapy hospitalizations, 220 (2.1%) developed DIC. In-hospital mortality was significantly higher in hospitalizations with DIC (22.7% vs 2.4%; adjusted odds ratio [aOR], 10.96; 95% confidence interval [CI], 4.78-25.09). DIC was associated with higher odds of acute kidney injury (aOR, 6.01), respiratory failure (aOR, 9.96), and shock (aOR, 18.55) and greater use of renal replacement therapy, mechanical ventilation, and vasopressors. DIC was also associated with higher odds of gastrointestinal hemorrhage (aOR, 12.41) and greater transfusion needs. DIC was associated with longer hospital stays ( = +17.6 days; P < .001) and higher hospitalization charges ( = +$523,323; P = .02).
DIC is an infrequent yet severe complication of CAR T-cell therapy, associated with increased mortality, organ dysfunction, critical care utilization, transfusion needs, prolonged hospitalization, and higher charges. These findings underscore the importance of clinical vigilance and early intervention strategies.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。