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:Acute kidney injury in hematological patients treated with CAR-T cells: risk factors, clinical presentation and impact on outcomes.
Acute kidney injury in hematological patients treated with CAR-T cells: risk factors, clinical presentation and impact on outcomes.
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CAR-T 细胞疗法彻底改变了血液系统恶性肿瘤的治疗,但也伴有显著风险,包括急性肾损伤(AKI)。本研究调查接受CAR-T 治疗患者发生AKI的危险因素及其临床影响。这项回顾性研究纳入接受CAR-T 治疗的血液系统疾病患者,收集临床和实验室数据,并在CAR-T 输注后随访期间监测临床结局。AKI按KDIGO标准定义。结局指标包括早期死亡率、总生存期(OS)和无病生存期(DFS)。分析的48例患者中,14例(29%)发生AKI,平均发生于CAR-T 输注后6天。AKI风险与基线体能状态相关(OR=8.65,95% CI:6.2–12,p=0.032),也与治疗后发生重度细胞因子释放综合征相关(OR=16.4,95% CI:1.9–138.5,p=0.01)。AKI患者更常需要重症监护。
此外,重度AKI是临床结局较差的独立相关因素,包括OS和DFS降低(HR=18.2,95% CI:2.6–27.3,p=0.003)。
此外,CAR-T 治疗后发生AKI的患者在随访期间更易进展为慢性肾病。总之,接受CAR-T 治疗的虚弱患者发生AKI的风险较高,且AKI可显著影响短期和长期结局。对这些患者而言,预防策略和早期识别AKI至关重要。
Chimeric antigen receptor T-cell (CAR-T) therapy has revolutionized the treatment of hematologic malignancies, yet it carries significant risks, including acute kidney injury (AKI). In this study, we investigated the risk factors and clinical impact of AKI in patients undergoing CAR-T cell therapy. This retrospective study involved hematologic patients treated with CAR-T therapy. Clinical and laboratory data were collected, and clinical outcomes were monitored during follow-up after CAR-T infusion.
AKI was defined according to KDIGO criteria. The outcome measures included early mortality, overall survival (OS), and disease-free survival (DFS). Among the 48 patients analyzed, 14 (29%) developed AKI, with a mean onset of 6 days after CAR-T infusion. The risk of AKI was associated with baseline performance status (OR 8. 65, IC95% 6. 2-12, p = 0. 032) and the development of severe cytokine release syndrome post-therapy (OR 16. 4 95%CI 1. 9-138. 5, p = 0. 01). Patients with AKI more frequently required intensive care.
Furthermore, severe AKI was independently associated with worse clinical outcomes, including reduced OS and DFS (HR 18. 2, 95%CI 2. 6-27. 3, p = 0. 003).
Additionally, patients who developed AKI post-CAR-T therapy were more likely to progress to chronic kidney disease during follow-up.
In conclusion, frail patients undergoing CAR-T therapy are at an increased risk of developing AKI, which can significantly affect both short- and long-term outcomes. Preventive strategies and early recognition of AKI are essential in these patients.
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