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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Atrial fibrillation is associated with increased in-hospitality mortality during Chimeric Antigen Receptor T-cell therapy hospitalizations: a retrospective cohort study in the United States.
Atrial fibrillation is associated with increased in-hospitality mortality during Chimeric Antigen Receptor T-cell therapy hospitalizations: a retrospective cohort study in the United States.
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在接受 CAR-T 治疗的癌症患者中,住院期间发生的 AF 与院内死亡、急性肺水肿、胃肠道出血、急性心力衰竭和住院时间延长的风险升高独立相关。
嵌合抗原受体(CAR)T细胞疗法(CAR-T)已成为治疗特定血液系统恶性肿瘤的一种有前景的方法。虽然一些研究提示CAR-T 与心房颤动(AF)之间存在关联,但仍需要更多数据来阐明AF与CAR-T 结局之间的关系。
这项回顾性队列研究利用2017—2020年全国住院患者样本(NIS),探讨了接受CAR-T 治疗的癌症合并AF患者的院内结局。研究比较了住院期间伴有AF与不伴有AF的患者,评估了包括死亡率、住院时长以及急性心力衰竭、肺水肿和胃肠道(GI)出血发生率在内的多项参数。
在236,270例癌症相关住院病例中,1,030例(0.44%)接受了CAR-T。CAR-T 接受者的平均年龄为55.6岁 18.1岁,女性占所有CAR-T 接受者的40.5%。在1030例接受CAR-T 的患者中,97例(9.4%)在住院期间伴有AF诊断。一项针对年龄、性别、种族、合并症和收入进行调整的多变量logistic回归分析显示,与接受CAR-T 但无AF的住院患者相比,接受CAR-T 治疗且伴有AF的住院癌症患者院内死亡(调整比值比,aOR:3.87)、急性肺水肿(aOR:3.29)、GI出血(aOR:5.46)、急性心力衰竭(aOR:10.2)和住院时间延长(Beta系数:0.18)的几率增加。在两项敏感性分析中观察到类似结果:一项仅限于弥漫性B细胞淋巴瘤患者,另一项排除了在接受CAR-T 治疗期间发生脓毒症或呼吸衰竭的患者。
Chimeric Antigen Receptor (CAR) T-cell therapy (CAR-T) has emerged as a promising treatment for specific hematological malignancies. While some studies suggest an association between CAR-T and atrial fibrillation (AF), more data are needed on the association of AF with CAR-T outcomes.
This retrospective cohort study utilized the National Inpatient Sample (NIS) 2017-2020 to explore in-hospital outcomes in cancer patients with AF while undergoing CAR-T. Comparisons were drawn between patients with and without AF during the hospitalization, assessing various parameters including mortality rates, length of hospital stay, and occurrences of acute heart failure, pulmonary edema, and gastrointestinal (GI) bleeding.
Of the 236,270 cancer-related hospitalizations, 1,030 cases (0.44%) received CAR-T. The average age of CAR-T recipients was 55.6 years 18.1 years, and females constituted 40.5% of the total CAR-T recipients. Of the 1030 patients receiving CAR-T, 97 (9.4%) had an associated diagnosis of AF during their hospitalization. A multivariable logistic regression analysis, adjusted for age, sex, race, comorbidity, and income, revealed that hospitalized cancer patients who underwent CAR-T therapy with AF had increased odds of in-hospital mortality (adjusted odds ratio, aOR: 3.87), acute pulmonary edema (aOR: 3.29), GI bleeding (aOR: 5.46), acute heart failure (aOR: 10.2), and extended hospital stays (Beta coefficient: 0.18) compared to hospitalizations with CAR-T but without AF. Similar results were observed in two sensitivity analyses: one limited to patients with diffuse B-cell lymphoma, and another excluding patients who had sepsis or respiratory failure while receiving CAR-T therapy.
In cancer patients receiving CAR-T, inpatient AF is independently associated with a higher risk of in-hospital mortality, acute pulmonary edema, gastrointestinal bleeding, acute heart failure, and prolonged hospitalization.
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