Department of Urology, Kindai University Faculty of Medicine, Osaka, Japan.
Anticancer Drugs. 2022 Jan 1;33(1):e818-e821. doi: 10.1097/CAD.0000000000001230.
Recently, combination therapy including immune checkpoint inhibition (ICI) has proven to be effective as first-line therapy for patients with metastatic renal cell carcinoma. Although the first-line combination therapies with ICI have shown clinical benefit, a number of patients require second-line treatment. We report a 60-year-old man with metastatic renal cell carcinoma who was treated with pazopanib soon after nivolumab plus ipilimumab combination therapy. He experienced Grade 3 disseminated intravascular coagulation (DIC). We suspect that this was caused by an interaction between pazopanib and nivolumab even though ICI therapy was discontinued. He was treated with thrombomodulin and platelet transfusion and recovered from DIC. Treatment with pazopanib was subsequently restarted. No evidence of DIC was observed thereafter. This severe adverse reaction may have been induced by an interaction between activated proinflammatory immune cells and cytokines from an exacerbated inflammatory state and pazopanib. This report highlights the need to perform careful monitoring of patients who receive molecular targeted therapy after ICI-based immunotherapy.
最近,包括免疫检查点抑制(ICI)在内的联合治疗已被证明对转移性肾细胞癌患者作为一线治疗有效。尽管具有 ICI 的一线联合治疗显示出了临床获益,但仍有许多患者需要二线治疗。我们报告了一名 60 岁男性转移性肾细胞癌患者,在纳武单抗加伊匹单抗联合治疗后很快接受了帕唑帕尼治疗。他出现了 3 级弥散性血管内凝血(DIC)。我们怀疑这是由帕唑帕尼与纳武单抗相互作用引起的,尽管已经停止了 ICI 治疗。他接受了血栓调节蛋白和血小板输注治疗,DIC 得到了缓解。随后重新开始使用帕唑帕尼治疗。此后未观察到 DIC 的证据。这种严重的不良反应可能是由激活的促炎免疫细胞与来自炎症加重状态的细胞因子和帕唑帕尼之间的相互作用引起的。本报告强调了在基于 ICI 的免疫治疗后接受分子靶向治疗的患者需要进行仔细监测的必要性。