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:Risk Factors, Prevalence, and Outcomes of Invasive Fungal Disease Post Hematopoietic Cell Transplantation and Cellular Therapies: A Retrospective Monocenter Real-Life Analysis.
Risk Factors, Prevalence, and Outcomes of Invasive Fungal Disease Post Hematopoietic Cell Transplantation and Cellular Therapies: A Retrospective Monocenter Real-Life Analysis.
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(1) 背景:自体、异基因造血细胞移植(HCT)以及其他细胞疗法,包括 CAR-T 细胞和基因治疗,构成了多种良性和恶性血液病管理的基石。侵袭性真菌感染(IFD)仍然是 HCT 受者发病和死亡的重要原因。
因此,我们研究了在新一代抗真菌预防时代,HCT 和其他细胞疗法后 IFD 的患病率和危险因素。(2) 方法:在本研究中,我们回顾性纳入了过去十年(2013-2022)在我们 JACIE 认证中心按照标准操作流程接受治疗的成人 HCT 受者。(3) 结果:共研究了 950 例接受细胞疗法的患者。19 例 CAR-T 细胞受者和 2 例基因治疗受者均未发生 IFD,而 456 例自体 HCT 受者中有 3 例患有原发性难治/复发性淋巴瘤的患者出现 probable IFD。
总体而言,接受异基因 HCT 的患者中有 11 例发生 probable IFD,473 例中有 31 例发现 possible IFD,473 例中有 10 例为 proven IFD。3 例患者出现第二次 IFD 发作。proven IFD 相比 probable IFD 的 4 年 OS 显著更低(p = 0.041),并且与 HCT-CI(p = 0.040)和慢性 GVHD(p = 0.045)独立相关。(4) 结论:在这个真实世界队列中,在新一代抗真菌预防时代,proven 和 probable IFD 的患病率相对较低。然而,IFD 与接受异基因 HCT 患者的不良结局相关。
(1) Background: Autologous, allogeneic hematopoietic cell transplantation (HCT) and other cellular therapies, including CAR T cell and gene therapy, constitute a cornerstone in the management of various benign and malignant hematological disorders. Invasive fungal infections (IFD) remain a significant cause of morbidity and mortality in HCT recipients.
Therefore, we investigated the prevalence and risk factors of IFD following HCT and other cellular therapies in an era of novel antifungal prophylaxis. (2) Methods: In this study, we retrospectively enrolled adult HCT recipients who were treated at our JACIE-accredited center according to standard operating procedures over the last decade (2013-2022).
(3) Results: 950 patients who received cellular therapies were studied. None of the 19 CAR T cell and neither of the two gene therapy recipients developed IFD whereas 3/456 autologous HCT recipients who suffered from primary refractory/relapsed lymphomas presented with probable IFD.
Overall, 11 patients who received allogeneic HCT experienced probable IFD, possible IFD was found in 31/473, and IFD was proven in 10/473. A second IFD episode was present in three patients. Four-year OS was significantly lower in proven compared to probable IFD ( p = 0. 041) and was independently associated with HCT-CI ( p = 0. 040) and chronic GVHD ( p = 0. 045). (4) Conclusions: In this real-world cohort, the prevalence of proven and probable IFD in an era of novel antifungal prophylaxis was found to be relatively low.
However, IFDs were associated with poor outcomes for patients who received allogeneic HCT.
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