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:Variance in development of early and late cardiotoxicities in patients with lymphoma and myeloma receiving CAR T-cell therapies.
Variance in development of early and late cardiotoxicities in patients with lymphoma and myeloma receiving CAR T-cell therapies.
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心血管不良事件(CVAE)是嵌合抗原受体(CAR)T细胞治疗已知并发症。然而,针对不同恶性肿瘤患者会发生哪些不良事件亚型的数据不足,且人们对CAR-T 治疗后不同心脏毒性最可能发生的时间范围知之甚少。本研究回顾性纳入211例接受CAR-T 治疗的患者,包括138例淋巴瘤患者和66例骨髓瘤患者。其中42例(19.9%)治疗后发生CVAE。骨髓瘤患者主要发生心力衰竭,淋巴瘤患者则主要发生心律失常。治疗后超过12个月仍可观察到严重CVAE。基线整体纵向应变较低与淋巴瘤及骨髓瘤患者CAR-T 治疗后CVAE发生显著相关。这些发现突显淋巴瘤和骨髓瘤患者CAR-T 治疗后心脏毒性的多种表现,也表明治疗前超声心动图风险分层及长期监测的重要性。
Cardiovascular adverse events (CVAEs) are recognized complications of chimeric antigen receptor (CAR) T-cell therapies.
However, data are lacking regarding subtypes of adverse events that develop in patients with different malignancies, and little is known about the timeframe in which different cardiotoxicities are most likely to occur post-CAR T-cell therapies. In this study, 211 patients, including 138 lymphoma patients and 66 myeloma patients who received CAR T-cell therapies were retrospectively identified.
Of these, 42 patients (19. 9%) developed CVAEs post-treatment. Myeloma patients predominantly experienced heart failure while lymphoma patients predominantly experienced arrhythmia. Severe CVAEs were observed even at >12 months post-treatment. Lower baseline global longitudinal strain was significantly associated with development of post-CAR T-cell therapy CVAEs in both lymphoma and myeloma patients.
These findings highlight the spectra of post-CAR T-cell cardiotoxicities in lymphoma and myeloma patients and the importance of echocardiography for pretreatment risk stratification and long-term surveillance.
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