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一名患有胃癌和强直性脊柱炎的患者在使用抗PD-1药物纳武单抗后发生噬血细胞性淋巴组织细胞增生症。

Haemophagocytic Lymphohistiocytosis Following the anti-PD-1 Nivolumab in a Patient with Gastric Cancer and Ankylosing Spondylitis.

作者信息

Long Clara, Al-Abdulmalek Abdulrahman, Lai Jonathan, Haegert David G, Isnard Stephane, Cournoyer Denis, Routy Jean-Pierre

机构信息

Department of Medicine, McGill University Health Centre, Montreal, Canada.

Department of Pathology, McGill University Health Centre, Montreal, Canada.

出版信息

Eur J Case Rep Intern Med. 2024 Mar 28;11(5):004370. doi: 10.12890/2024_004370. eCollection 2024.

Abstract

BACKGROUND

Autoimmune diseases are not contraindications for immune checkpoint inhibitors (ICI) therapy in patients with cancer. However, immune-related adverse events (irAEs) are frequently observed in patients receiving ICIs including dermatitis, thyroiditis, colitis, and pneumonitis. Thrombocytopenic purpura, aplasia, and haemophagocytic lymphohistiocytosis (HLH) are rarely observed during ICIs.

CASE DESCRIPTION

We report the case of a male patient with pre-existing untreated HLA B27 and ankylosing spondylitis with gastric cancer and liver metastases. The 79-year-old man was treated with anti-HER2 trastuzumab and anti-PD-1 nivolumab. Seventeen days after the seventh cycle of treatment, he presented at the emergency department with acute fever, confusion, and hypotension. Laboratory results showed pancytopenia, and elevation of ferritin and triglyceride. No infections were detected. Although not seen in a bone marrow biopsy, clinical presentation, and absence of infection, together with an H-score of 263, indicated HLH. The patient was treated with dexamethasone for four days and discharged on a tapering dose of steroids. At the two-month follow-up, clinical presentation was normal and blood test almost normalised. At 8 months, no liver metastases were observed.

CONCLUSIONS

In a patient with a pre-existing autoimmune condition, immunotherapy led to the development of HLH, which was controlled by glucocorticoid. Absence of the feature of haemophagocytosis in the bone marrow biopsy did not exclude the diagnosis, as HLH can occur in the spleen or in the liver. Glucocorticoid therapy did not prevent the anti-cancer effect of ICIs, and liver metastases disappeared 8 months post-HLH. This case warrants further research on the interplay between autoimmunity and ICI response, as well as ICI-induced irAEs.

LEARNING POINTS

Haemophagocytic lymphohistiocytosis (HLH) post seventh cycle of trastuzumab (anti-HER2) and nivolumab (anti-PD-1) was controlled with glucocorticoid.Breach of tolerance was due to immunotherapy-induced HLH in a patient with pre-existing autoimmune condition (HLA B27- positive ankylosing spondylitis).There was a complete disappearance of liver metastases 8 months post-HLH.

摘要

背景

自身免疫性疾病并非癌症患者免疫检查点抑制剂(ICI)治疗的禁忌证。然而,接受ICI治疗的患者中经常会观察到免疫相关不良事件(irAE),包括皮炎、甲状腺炎、结肠炎和肺炎。在ICI治疗期间,血小板减少性紫癜、再生障碍性贫血和噬血细胞性淋巴组织细胞增生症(HLH)很少见。

病例描述

我们报告了一例患有未经治疗的HLA B27和强直性脊柱炎且伴有胃癌和肝转移的男性患者。这名79岁的男性接受了抗HER2曲妥珠单抗和抗PD-1纳武单抗治疗。在第七周期治疗后的第17天,他因急性发热、意识模糊和低血压到急诊科就诊。实验室检查结果显示全血细胞减少,铁蛋白和甘油三酯升高。未检测到感染。尽管骨髓活检未发现噬血细胞现象,但临床表现及无感染情况,结合H评分263,提示HLH。患者接受地塞米松治疗4天,然后逐渐减量的类固醇药物出院。在两个月的随访中,临床表现正常,血液检查几乎恢复正常。在8个月时,未观察到肝转移。

结论

在一名患有自身免疫性疾病的患者中,免疫治疗导致了HLH的发生,该疾病通过糖皮质激素得到控制。骨髓活检中未出现噬血细胞特征并不排除诊断,因为HLH可发生在脾脏或肝脏中。糖皮质激素治疗并未阻止ICI的抗癌作用,且HLH发生8个月后肝转移消失。该病例值得进一步研究自身免疫与ICI反应之间的相互作用以及ICI诱导的irAE。

学习要点

曲妥珠单抗(抗HER2)和纳武单抗(抗PD-1)第七周期治疗后发生的噬血细胞性淋巴组织细胞增生症(HLH)通过糖皮质激素得到控制。在一名患有既往自身免疫性疾病(HLA B27阳性强直性脊柱炎)的患者中,免疫治疗导致的HLH引发了免疫耐受的突破。HLH发生8个月后肝转移完全消失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90ec/11073590/2d0df60ae9ff/4370_Fig1.jpg

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