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:Less frequent complications following CAR T-cell therapies: hemophagocytic lymphohistiocytosis, graft-versus-host disease, thrombotic microangiopathy, coagulation disorders and secondary malignancies: best practice recommendations from the EBMT Practice Harmonization and Guidelines Committee.
Less frequent complications following CAR T-cell therapies: hemophagocytic lymphohistiocytosis, graft-versus-host disease, thrombotic microangiopathy, coagulation disorders and secondary malignancies: best practice recommendations from the EBMT Practice Harmonization and Guidelines Committee.
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CAR-T 细胞疗法已改变血液系统恶性肿瘤的治疗格局,但除已知的细胞因子释放综合征(CRS)、神经毒性、免疫效应细胞相关血液毒性(ICAHT)和感染外,其他非典型毒性也逐渐显现。本综述由欧洲血液和骨髓移植学会(EBMT)实践协调与指南委员会制定,讨论CAR-T 治疗后其他重要并发症的管理,包括噬血细胞性淋巴组织细胞增多症(HLH)、移植物抗宿主病(GvHD)、血栓性微血管病(TMA)、凝血障碍及继发恶性肿瘤。这些并发症虽不常见,却构成重大挑战,常导致发病和死亡,目前尚无标准化管理方案。本文基于有限但不断涌现的临床证据,提出早期识别、风险降低及治疗干预的最佳实践建议。对于这些研究不足的CAR-T 相关毒性,全面的专家指导对优化管理至关重要。
CAR T-cell therapies have revolutionized the treatment of hematologic malignancies; however, alongside the well-known complications of cytokine release syndrome (CRS), neurotoxicity, immune effector cell-associated hematotoxicity (ICAHT), and infections, other non-classical toxicities are emerging. This review, developed by the EBMT Practice Harmonization and Guidelines Committee, addresses the management of other critical post-CAR T-cell complications including hemophagocytic lymphohistiocytosis (HLH), graft-versus-host disease (GvHD), thrombotic microangiopathy (TMA), coagulation disorders and secondary malignancies.
These complications, though less frequent, present a significant challenge, often contributing to morbidity and mortality with no standardized management protocols. This review provides best practice recommendations for early identification, risk mitigation, and therapeutic interventions, supported by limited but emerging clinical evidence. Comprehensive expert guidance is essential for optimal management of these under-explored toxicities following CAR T-cell therapies.
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