首页> 外文期刊>Journal for ImmunoTherapy of Cancer >A case of dual-mechanism immune-related anaemia in a patient with metastatic melanoma treated with nivolumab and ipilimumab
【24h】

A case of dual-mechanism immune-related anaemia in a patient with metastatic melanoma treated with nivolumab and ipilimumab

机译:用Nivolumab和Ipilimalab治疗转移性黑素瘤的患者双机制免疫相关贫血的情况

获取原文
获取外文期刊封面目录资料

摘要

Background The combination of the immune checkpoint inhibitors (ICIs) ipilimumab and nivolumab is a mainstay of treatment for selected patients with metastatic melanoma. This combination also results in more frequent immune-related adverse events (irAEs) than either ICI alone. These irAEs can be severe and their pathogenesis is poorly understood. Case presentation We report a case of a woman with metastatic melanoma, treated with combined ipilimumab and nivolumab, who developed severe anaemia. While initial workup revealed autoimmune haemolytic anaemia, the anaemia persisted despite corticosteroids and paradoxical reticulocytopenia was observed. Bone marrow biopsy demonstrated a CD8 T cell-mediated destruction of the red cell precursors implying concurrent pure red cell aplasia. Both processes resolved after the addition of cyclosporine A. Conclusions This report describes a rare case of two concurrent mechanisms of haematological irAE in a patient treated with combined ICI therapy. Successful treatment resulted only after the second underlying mechanism of toxicity was uncovered. Prompt recognition of these unusual presentations of rare irAEs is now key to effective irAE management.
机译:背景技术免疫检查点抑制剂(ICIS)IPILIMIMAB和NIVOLUMAB的组合是对选定的转移性黑素瘤患者的治疗方法。这种组合还会导致比单独的ICI更频繁的免疫相关的不良事件(IRAES)。这些伊拉斯可能是严重的,并且他们的发病机制很难理解。案例介绍我们报告了一种患有转移性黑素瘤的女性的案例,用合并的IPILIMIMAB和Nivolumab进行治疗,他们开发出严重贫血。虽然初始次处理揭示了自身免疫血液解性贫血,但贫血仍然存在尽管皮质类固醇和矛盾的网状细胞缺乏症。骨髓活检表明了CD8 T细胞介导的红细胞前体的破坏,暗示同时纯红色细胞APLASIA。两种过程在加入环孢菌素A后解决了。结论本报告描述了少数罕见的ICI治疗治疗治疗患者中的血液学IRAE两种并发机制。只有在发现第二个毒性的毒性机制之后,才会成功治疗。迅速承认这些不寻常的罕见伊拉斯的陈述现在是有效的IRAE管理的关键。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号