医学
阿纳基纳
细胞因子释放综合征
巨噬细胞活化综合征
依托泊苷
托珠单抗
内科学
并发症
化疗
胃肠病学
外科
免疫学
嵌合抗原受体
免疫疗法
癌症
关节炎
疾病
作者
Jean‐Jacques Tudesq,Mathilde Yakoub-Agha,Jacques‐Olivier Bay,Corinne Courbon,Franciane Paul,Muriel Picard,Cécile Pochon,Arthur Sterin,Céline Vicente,Emmanuel Canet,Ibrahim Yakoub‐Agha,Anne‐Sophie Moreau
标识
DOI:10.1016/j.bulcan.2021.11.002
摘要
The use of chimeric antigen receptor T cells (CAR-T) has increased since their approval in the treatment of several relapsed/refractory B cell malignancies. The management of their specific toxicities, such as cytokine release syndrome (CRS), tends to be better understood and well-defined. During the twelfth edition of practice harmonization workshops of the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC), a working group focused its work on the management of patients developing CRS following CAR-T cell therapy. A special chapter has been allocated to macrophage activation syndrome (MAS), a rare but life-threatening complication post-CAR-T. In addition to symptomatic measures and preemptive broad-spectrum antibiotics, immunomodulators such as tocilizumab and corticosteroids remain the corner stone for the treatment of CRS. Tocilizumab/corticosteroids-resistant CRS associated with haemophagocytosis markers (spleen and liver enlargement, hyperferritinaemia>10,000ng/mL, hypofibrinogenemia…) should direct the diagnosis towards an overlapping CRS/MAS. An adapted treatment will be based on high-dose IV anakinra and corticosteroids and chemotherapy with etoposide at late refractory stages. These complications and others delignate the need of close collaboration with an intensive care unit.
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