Hemophagocytic Lymphohistiocytosis (HLH) Following Immune Checkpoint Therapy (ICT).

IF 0.6 Q4 ONCOLOGY Case Reports in Oncological Medicine Pub Date : 2025-01-06 eCollection Date: 2025-01-01 DOI:10.1155/crom/5582848
Saivaroon Gajagowni, Emily Wang, Jianbo Wang, Matthew T Campbell, Bilal A Siddiqui
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Abstract

In the past decade, the use of immune checkpoint therapy (ICT) has increased across many malignancies, including metastatic renal cell carcinoma as an option for frontline and subsequent lines of therapy. Despite the many therapeutic benefits of ICT, its use is complicated by the potential risk of immune-related adverse events (irAEs). One rare but potentially life-threatening irAE is hemophagocytic lymphohistiocytosis (HLH). HLH is a systemic inflammatory disorder resulting in multiorgan failure. The diagnosis of HLH is a challenge due to nonspecific symptoms and overlap with other systemic conditions, which can lead to delays in receiving appropriate treatment and potentially poor patient outcomes. This case illustrates the management of HLH caused by nivolumab plus ipilimumab combination therapy through the use of corticosteroids and tocilizumab in a patient with metastatic clear cell renal cell carcinoma.

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免疫检查点治疗(ICT)后的噬血细胞淋巴组织细胞病(HLH)。
在过去的十年中,免疫检查点疗法(ICT)的使用在许多恶性肿瘤中都有所增加,包括转移性肾细胞癌作为一线和后续治疗的选择。尽管ICT具有许多治疗益处,但其使用因免疫相关不良事件(irAEs)的潜在风险而变得复杂。一种罕见但可能危及生命的irAE是噬血细胞性淋巴组织细胞增多症(HLH)。HLH是一种导致多器官衰竭的全身性炎症性疾病。由于非特异性症状和与其他全身性疾病的重叠,HLH的诊断是一项挑战,这可能导致接受适当治疗的延误和潜在的不良患者预后。该病例说明了在转移性透明细胞肾细胞癌患者中,通过使用皮质类固醇和托珠单抗,尼伏单抗加伊匹单抗联合治疗引起的HLH的管理。
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来源期刊
自引率
0.00%
发文量
11
审稿时长
16 weeks
期刊介绍: Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.
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