| Literature DB >> 31571160 |
Hongli Chen1, Fangxia Wang1, Pengyu Zhang1, Yilin Zhang1, Yinxia Chen1, Xiaohu Fan2, Xingmei Cao1, Jie Liu1, Yun Yang1, Baiyan Wang1, Bo Lei1, Liufang Gu1, Ju Bai1, Lili Wei1, Ruili Zhang1, Qiuchuan Zhuang2, Wanggang Zhang3, Wanhong Zhao4, Aili He5.
Abstract
Chimeric antigen receptor T (CAR-T) cell therapy is a novel cellular immunotherapy that is widely used to treat hematological malignancies, including acute leukemia, lymphoma, and multiple myeloma. Despite its remarkable clinical effects, this therapy has side effects that cannot be underestimated. Cytokine release syndrome (CRS) is one of the most clinically important and potentially life-threatening toxicities. This syndrome is a systemic immune storm that involves the mass cytokines releasing by activated immune cells. This phenomenon causes multisystem damages and sometimes even death. In this study, we reported the management of a patient with recurrent and refractory multiple myeloma and three patients with acute lymphocytic leukemia who suffered CRS during CAR-T treatment. The early application of tocilizumab, an anti-IL-6 receptor antibody, according to toxicity grading and clinical manifestation is recommended especially for patients who suffer continuous hyperpyrexia, hypotensive shock, acute respiratory failure, and whose CRS toxicities deteriorated rapidly. Moreover, low doses of dexamethasone (5-10 mg/day) were used for refractory CRS not responding to tocilizumab. The effective management of the toxicities associated with CRS will bring additional survival opportunities and improve the quality of life for patients with cancer.Entities:
Keywords: chimeric antigen receptor T cell; cytokine release syndrome; tocilizumab
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Year: 2019 PMID: 31571160 DOI: 10.1007/s11684-019-0714-8
Source DB: PubMed Journal: Front Med ISSN: 2095-0217 Impact factor: 4.592