Case Report: Immune checkpoint inhibitor-induced multiorgan vasculitis successfully treated with rituximab.

Sehrish Qureshi, Naszrin Arani, Vishnu Parvathareddy, Amanda Tchakarov, Maen Abdelrahim, Maria Suarez-Almazor, Jianjun Zhang, Don Lynn Gibbons, John Heymach, Mehmet Altan, Ala Abudayyeh
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Abstract

Immune checkpoint inhibitors (ICIs) have revolutionized the treatment of cancer. ICIs have a unique side effect profile, generally caused by inflammatory tissue damage, with clinical features similar to autoimmune conditions. Acute kidney injury from ICIs has been well studied; incidence ranges from 1% to 5%, with higher incidence when combination ICI therapies are used. Although the overall reported incidence of ICI-associated glomerulonephritis is less than 1%, vasculitis is the most commonly reported ICI-related glomerulonephritis. Other biopsy findings include thrombotic microangiopathy, focal segmental glomerulosclerosis, minimal change disease, and IgA nephropathy with secondary amyloidosis. We report a case in which a woman previously treated with the PD-L1 inhibitor durvalumab for locally advanced non-small cell lung cancer with pre-existing antineutrophil cytoplasmic (anti-PR3) antibody who later developed multi-organ vasculitis after ICI exposure, which was successfully treated with rituximab, with continued cancer remission for 3 years.

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病例报告:利妥昔单抗成功治疗免疫检查点抑制剂诱导的多器官血管炎。
免疫检查点抑制剂(ICIs)已经彻底改变了癌症的治疗。ICIs具有独特的副作用,通常由炎症组织损伤引起,其临床特征与自身免疫性疾病相似。ICIs引起的急性肾损伤已经得到了很好的研究;发病率从1%到5%不等,当联合使用ICI治疗时发病率更高。虽然总体报道的ici相关肾小球肾炎发病率不到1%,但血管炎是最常报道的ici相关肾小球肾炎。其他活检结果包括血栓性微血管病、局灶节段性肾小球硬化、微小病变和IgA肾病伴继发性淀粉样变性。我们报告了一个病例,一名妇女先前使用PD-L1抑制剂durvalumab治疗局部晚期非小细胞肺癌,先前存在抗中性粒细胞细胞质(抗pr3)抗体,后来在ICI暴露后发展为多器官血管炎,利妥昔单抗成功治疗,癌症持续缓解3年。
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