Nivolumab和Ipilimumab联合免疫治疗一名黑色素瘤患者的噬血细胞淋巴组织细胞增多症的有效治疗。

Q4 Biochemistry, Genetics and Molecular Biology
R. Pacholczak-Madej, A. Grela-Wojewoda, Joanna Lompart, B. Żuchowska-Vogelgesang, M. Ziobro
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引用次数: 6

摘要

免疫检查点抑制剂显著改善了黑色素瘤患者的预后。然而,这些疗法可能引发意想不到的免疫相关不良事件(irAEs),这在做出正确的诊断和提供治疗方面具有挑战性。血液学毒性是可能的irAEs,但在临床试验中评价不佳,针对这一特定并发症的治疗建议有限。我们报告了一位IV期黑色素瘤患者,在纳武单抗和伊匹单抗联合免疫治疗第4个疗程后出现了极其罕见的毒性-噬血细胞性淋巴组织细胞增多症(HLH)。患者对类固醇有抵抗性,只有用各种免疫抑制剂治疗才能控制病情,最终使黑色素瘤消退。在本报告中,我们评估了治疗HLH的方法,并描述了我们对现有方案的修改。立即免疫抑制可以挽救生命,由于这种情况的罕见性以及缺乏具体建议,每一份报告对临床医生都很有价值,特别是在治疗有效的情况下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effective Treatment of a Melanoma Patient with Hemophagocytic Lymphohistiocytosis after Nivolumab and Ipilimumab Combined Immunotherapy.
Immune checkpoint inhibitors have significantly improved the prognosis of melanoma patients. However, these therapies may trigger unexpected immune-related adverse events (irAEs), which are challenging in making the proper diagnosis and providing treatment. Hematological toxicities are possible irAEs, but were poorly evaluated in clinical trials and treatment recommendations of this specific complications are limited. We present a stage IV melanoma patient who developed an extremely rare toxicity - hemophagocytic lymphohistiocytosis (HLH) after the 4th course of combined immunotherapy with nivolumab and ipilimumab. The patient was steroid resistant and only the treatment with various immunosuppressive agents provided control of the disease and finally melanoma regression. In this report, we evaluated the methods of HLH treatment and described our modification of available protocols. Immediate immunosuppression can be life-saving and due to rarity of this condition as well as lack of specific recommendations, every report is valuable for clinicians, especially when treatment was effective.
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来源期刊
Prague medical report
Prague medical report Medicine-Medicine (all)
CiteScore
1.10
自引率
0.00%
发文量
19
审稿时长
20 weeks
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