Sjogren's syndrome due to immune checkpoint inhibitors (ICIs): Insights from a single-institution series and systematic review of the literature.

IF 1 4区 医学 Q4 ONCOLOGY Journal of Oncology Pharmacy Practice Pub Date : 2024-08-08 DOI:10.1177/10781552241271753
Abram Soliman, Ruba Hassan, Ion Codreanu, Steven C Plaxe, Constantin A Dasanu
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Abstract

Introduction: Careful adverse event assessment and management are important when prescribing immune checkpoint inhibitors (ICIs) to cancer patients. Iatrogenic Sjogren's syndrome is a relatively rare immune-related adverse event (irAEs) that affects the moisture-producing glands.

Methods: We describe a series of four patients who developed Sjogren's syndrome while being treated with ICIs at a community cancer center in Southern California, USA (1/1/2017-12/31/2023). Patient, drug and disease-related data were collected by retrospective chart review. A systematic search of the PubMed database was performed to identify similar cases in the literature (1/1/2016-12/31//2023).

Results: Of 224 cancer patients at our center treated with ICIs, four (1.8%) developed iatrogenic Sjogren's syndrome. All of our patients were male; three received PD-1 inhibitors (nivolumab, pembrolizumab) and one received the PD-L1 inhibitor atezolizumab. The median time to development of Sjogren's syndrome was 24 weeks (range, 8-36 weeks); dry mouth symptoms were more prominent than dry eye symptoms. None of the patients had elevated SS-A, SS-B or antinuclear antibodies. One patient developed multiple tooth cavities and had several extractions, due to severe xerostomia. Management of all patients was primarily symptomatic. Two cases were irreversible; one was reversible and the 4th case is undermined as he is still on ICI therapy. Our systematic review of the literature identified 80 cases in five articles. Incidence of xerostomia was twice of that of xerophthalmia. The male/female ratio was 1.5:1. SS-A, SS-B, or antinuclear antibodies were found in only 9% of patients. Steroids were reported to have had only a limited role in management.

Conclusions: The incidence of Sjogren's syndrome due to ICIs in our center was 1.8%. Details of clinical course and management in these patients are presented. Caring for patients with ICI-related Sjogren's syndrome is facilitated by a multidisciplinary effort including oncologists, otolaryngologists, dentists, ophthalmologists and rheumatologists. Expanding the knowledge base pertaining to iatrogenic Sjogren's syndrome in patients on ICIs will be helpful in promoting early detection and treatment, and improving outcomes.

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免疫检查点抑制剂(ICIs)导致的 Sjogren's 综合征:单个机构系列研究的启示和文献的系统回顾。
简介在为癌症患者开具免疫检查点抑制剂(ICIs)处方时,仔细评估和管理不良事件非常重要。先天性Sjogren综合征是一种相对罕见的免疫相关不良事件(irAEs),会影响湿润腺体:我们描述了在美国南加州一家社区癌症中心接受 ICIs 治疗期间(2017 年 1 月 1 日至 2023 年 12 月 31 日)发生 Sjogren's 综合征的四名患者。通过回顾性病历审查收集了患者、药物和疾病相关数据。对PubMed数据库进行了系统检索,以确定文献中的类似病例(1/1/2016-12/31/2023):在本中心接受 ICIs 治疗的 224 例癌症患者中,有 4 例(1.8%)出现了先天性 Sjogren's 综合征。所有患者均为男性;三人接受了PD-1抑制剂(nivolumab、pembrolizumab)治疗,一人接受了PD-L1抑制剂atezolizumab治疗。出现 Sjogren's 综合征的中位时间为 24 周(8-36 周不等);口干症状比眼干症状更为突出。没有一名患者出现 SS-A、SS-B 或抗核抗体升高。一名患者因严重的口腔干燥症而出现多个龋齿,并进行了数次拔牙手术。所有患者均以对症治疗为主。其中两例不可逆,一例可逆,第四例由于仍在接受 ICI 治疗,因此病情不乐观。我们对文献进行了系统性回顾,在 5 篇文章中发现了 80 个病例。口干症的发病率是眼干症的两倍。男女比例为 1.5:1。只有 9% 的患者发现 SS-A、SS-B 或抗核抗体。据报道,类固醇在治疗中的作用有限:结论:在我们中心,因 ICIs 引起的 Sjogren's 综合征的发病率为 1.8%。本文详细介绍了这些患者的临床病程和治疗方法。肿瘤科、耳鼻喉科、牙科、眼科和风湿免疫科等多学科专家的合作有助于治疗 ICI 相关 Sjogren's 综合征患者。扩大与使用 ICIs 患者的先天性 Sjogren's 综合征相关的知识库将有助于促进早期发现和治疗,并改善预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.70
自引率
7.70%
发文量
276
期刊介绍: Journal of Oncology Pharmacy Practice is a peer-reviewed scholarly journal dedicated to educating health professionals about providing pharmaceutical care to patients with cancer. It is the official publication of the International Society for Oncology Pharmacy Practitioners (ISOPP). Publishing pertinent case reports and consensus guidelines...
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