Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD;
Seattle Children's Hospital, Seattle, WA;
Blood. 2014 Jul 10;124(2):188-95. doi: 10.1182/blood-2014-05-552729. Epub 2014 May 29.
As immune-based therapies for cancer become potent, more effective, and more widely available, optimal management of their unique toxicities becomes increasingly important. Cytokine release syndrome (CRS) is a potentially life-threatening toxicity that has been observed following administration of natural and bispecific antibodies and, more recently, following adoptive T-cell therapies for cancer. CRS is associated with elevated circulating levels of several cytokines including interleukin (IL)-6 and interferon γ, and uncontrolled studies demonstrate that immunosuppression using tocilizumab, an anti-IL-6 receptor antibody, with or without corticosteroids, can reverse the syndrome. However, because early and aggressive immunosuppression could limit the efficacy of the immunotherapy, current approaches seek to limit administration of immunosuppressive therapy to patients at risk for life-threatening consequences of the syndrome. This report presents a novel system to grade the severity of CRS in individual patients and a treatment algorithm for management of CRS based on severity. The goal of our approach is to maximize the chance for therapeutic benefit from the immunotherapy while minimizing the risk for life threatening complications of CRS.
随着癌症的免疫疗法变得更有效、更广泛可用,管理其独特毒性的最佳方法变得越来越重要。细胞因子释放综合征(CRS)是一种潜在的危及生命的毒性反应,在使用天然和双特异性抗体以及最近使用过继性 T 细胞疗法治疗癌症后均有观察到。CRS 与几种细胞因子(包括白细胞介素(IL)-6 和干扰素 γ)的循环水平升高有关,非对照研究表明,使用抗白细胞介素 6 受体抗体托珠单抗联合或不联合皮质类固醇的免疫抑制治疗可以逆转该综合征。然而,由于早期和积极的免疫抑制可能会限制免疫疗法的疗效,目前的方法旨在将免疫抑制治疗的给药限制在有发生危及生命的综合征后果风险的患者。本报告提出了一种新的系统,用于对个体患者的 CRS 严重程度进行分级,并提出了一种基于严重程度的 CRS 管理治疗算法。我们方法的目标是最大限度地提高免疫疗法的治疗获益机会,同时最大限度地降低 CRS 危及生命并发症的风险。