Albany Medical College, Albany, New York.
Weill Cornell Medicine, New York, NY.
J Clin Rheumatol. 2021 Dec 1;27(8):e317-e322. doi: 10.1097/RHU.0000000000001370.
We performed a systematic literature review to identify all reports of immune checkpoint inhibitor-associated inflammatory arthritis to describe it phenotypically and serologically.
PubMed, Embase, and Cochrane databases were searched for reports of musculoskeletal immune-related adverse events secondary to ICI treatment. Publications were included if they provided individual patient level data regarding the pattern of joint involvement. Descriptive statistics were used to summarize results.
A total of 4339 articles were screened, of which 67 were included, encompassing 372 patients. The majority of patients had metastatic melanoma (57%), and they were treated with anti-PD1 or anti-PDL1 therapy (78%). Median time to onset of arthritis was 4 months (range, 1 day to 53 months). Forty-nine percent had polyarthritis, 17% oligoarthritis, 3% monoarthritis, 10% arthralgia, and 21% polymyalgia rheumatica. More than half of patients were described as having a "rheumatoid arthritis-like" presentation. Nine percent tested positive for rheumatoid factor or anti-cyclic citrullinated peptide antibodies. Seventy-four percent required corticosteroids, and 45% required additional medications. Sixty-three percent achieved arthritis control, and 32% were ultimately able to discontinue antirheumatic treatments. Immune checkpoint inhibitors were continued in 49%, transiently withheld in 11%, and permanently discontinued due to musculoskeletal immune-related adverse events in 13%.
Half of reported immune checkpoint inhibitor-associated arthritis cases present with polyarthritis (often RA-like), but only 9% are seropositive. Polymyalgia rheumatica is also common. Most patients respond to steroids alone, but about half require additional medications. Further studies are needed to determine long-term musculoskeletal outcomes in these patients, and the impact of arthritis treatment on cancer survival.
我们进行了系统的文献回顾,以确定所有免疫检查点抑制剂相关炎症性关节炎的报告,以描述其表型和血清学特征。
检索 PubMed、Embase 和 Cochrane 数据库中与 ICI 治疗相关的肌肉骨骼免疫相关不良事件的报告。如果出版物提供了关于关节受累模式的个体患者水平数据,则将其纳入。使用描述性统计数据总结结果。
共筛选了 4339 篇文章,其中 67 篇被纳入,共纳入 372 例患者。大多数患者患有转移性黑色素瘤(57%),并接受了抗 PD1 或抗 PDL1 治疗(78%)。关节炎发病的中位时间为 4 个月(范围,1 天至 53 个月)。49%的患者有多发性关节炎,17%的患者为少发性关节炎,3%的患者为单发性关节炎,10%的患者为关节痛,21%的患者为多发性肌痛。超过一半的患者被描述为表现出“类风湿关节炎样”表现。9%的患者类风湿因子或抗环瓜氨酸肽抗体阳性。74%的患者需要使用皮质类固醇,45%的患者需要额外的药物治疗。63%的患者关节炎得到控制,32%的患者最终能够停止抗风湿治疗。49%的患者继续使用免疫检查点抑制剂,11%的患者暂时停药,由于肌肉骨骼免疫相关不良事件,13%的患者永久停药。
报告的免疫检查点抑制剂相关关节炎病例中,有一半表现为多发性关节炎(常为类风湿关节炎样),但只有 9%的患者血清学阳性。多发性肌痛也很常见。大多数患者单独使用类固醇即可缓解,但约一半的患者需要额外的药物治疗。需要进一步研究以确定这些患者的长期肌肉骨骼结局,以及关节炎治疗对癌症生存的影响。