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。

Sehrish Qureshi, Naszrin Arani, Vishnu Parvathareddy, Amanda Tchakarov, Maen Abdelrahim, Maria Suarez-Almazor, Jianjun Zhang, Don Lynn Gibbons, John Heymach, Mehmet Altan, Ala Abudayyeh
{"title":"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。","authors":"Sehrish Qureshi,&nbsp;Naszrin Arani,&nbsp;Vishnu Parvathareddy,&nbsp;Amanda Tchakarov,&nbsp;Maen Abdelrahim,&nbsp;Maria Suarez-Almazor,&nbsp;Jianjun Zhang,&nbsp;Don Lynn Gibbons,&nbsp;John Heymach,&nbsp;Mehmet Altan,&nbsp;Ala Abudayyeh","doi":"10.3389/fneph.2023.1168614","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":73091,"journal":{"name":"Frontiers in nephrology","volume":"3 ","pages":"1168614"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10479603/pdf/","citationCount":"0","resultStr":"{\"title\":\"Case Report: Immune checkpoint inhibitor-induced multiorgan vasculitis successfully treated with rituximab.\",\"authors\":\"Sehrish Qureshi,&nbsp;Naszrin Arani,&nbsp;Vishnu Parvathareddy,&nbsp;Amanda Tchakarov,&nbsp;Maen Abdelrahim,&nbsp;Maria Suarez-Almazor,&nbsp;Jianjun Zhang,&nbsp;Don Lynn Gibbons,&nbsp;John Heymach,&nbsp;Mehmet Altan,&nbsp;Ala Abudayyeh\",\"doi\":\"10.3389/fneph.2023.1168614\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":73091,\"journal\":{\"name\":\"Frontiers in nephrology\",\"volume\":\"3 \",\"pages\":\"1168614\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10479603/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in nephrology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3389/fneph.2023.1168614\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in nephrology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fneph.2023.1168614","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信