Department of Dermatology, University Hospital of Zurich.
Faculty of Medicine, University of Zurich, Zurich, Switzerland.
J Immunother. 2019 Jan;42(1):29-32. doi: 10.1097/CJI.0000000000000236.
Switching from immunotherapy to targeted therapy in metastasized melanoma can be complicated by a cytokine release syndrome (CRS). CRS is a serious complication, which is induced by high levels of circulating cytokines, associated with T-cell engagement and proliferation, and results in a constellation of symptoms with variable organ involvement. We report 2 patients with BRAF V600 mutant melanoma who were previously treated with anti-PD-1±anti-LAG-3 antibodies and were switched to BRAF/MEK-inhibitors because of progressive disease. Both cases depict the complexity of interactions occurring during sequential treatment with immune checkpoint inhibitors and kinase inhibitors. Early identification and management of CRS is crucial to decrease its toxicity and improve safety of further drugs to be given in a therapeutic ladder.
转移性黑色素瘤从免疫治疗转换为靶向治疗可能会因细胞因子释放综合征(CRS)而变得复杂。CRS 是一种严重的并发症,由循环细胞因子水平升高引起,与 T 细胞的参与和增殖有关,导致一系列症状,并伴有不同的器官受累。我们报告了 2 例 BRAF V600 突变型黑色素瘤患者,他们之前曾接受过抗 PD-1±抗 LAG-3 抗体治疗,由于疾病进展而改用 BRAF/MEK 抑制剂。这两种情况都描绘了在免疫检查点抑制剂和激酶抑制剂序贯治疗过程中发生的相互作用的复杂性。早期识别和管理 CRS 对于降低其毒性并提高治疗阶梯中给予的其他药物的安全性至关重要。