Creţu Ioana, Bojincă Mihai, Milicescu Mihaela, Cursaru Adrian, Șerban Bogdan, Crețu Bogdan, Iordache Sergiu, Pop Corina Silvia, Cîrstoiu Cătălin, Ionescu Ruxandra
Department of Internal Medicine and Rheumatology, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania.
Department of Internal Medicine and Rheumatology, 'Dr. Ion Cantacuzino' Hospital, 917151 Bucharest, Romania.
Exp Ther Med. 2021 Sep;22(3):1027. doi: 10.3892/etm.2021.10459. Epub 2021 Jul 16.
Immunotherapy has revolutionized cancer treatment. Immune checkpoint inhibitors (ICIs) including antibodies targeting cytotoxic T lymphocyte associated antigen-4 and programmed cell death 1 have been shown to be effective in the treatment of certain types of cancer. The benefit of these therapies is to prolong life expectancy in the case of metastatic malignancies. Rheumatic adverse events are not very common. In the present study, 9 patients were monitored between November 2018 and January 2020. The oncologist, who identified the occurrence of rheumatic toxicities after the treatment with ICIs, evaluated the patients. Only oncological patients with rheumatic manifestations after the start of immunotherapy were included. Toxicity grading was performed by both the oncologist and the rheumatologist, on a scale from 1 to 5 (1, mild; 2, moderate; 3, severe; 4, life-threatening; 5, death related to toxicity). The results showed that rheumatoid factor, which was sampled in each patient, was negative in all cases. Patients were treated with nonsteroidal anti-inflammatory drugs or prednisone depending on the severity of the adverse events. The results varied with the severity of the adverse events. In conclusion, as the number of patients treated with ICIs increases, so will the number of patients presenting with immune-related adverse events (irAEs). The collaboration between oncologists and rheumatologists should be intimate to provide optimal treatment to patients. Musculoskeletal manifestations secondary to ICIs are slightly different from other rheumatologically conditions making diagnosis, treatment and monitoring difficult. Thus, irAEs are new and challenging for oncologists, thus understanding of the pathogenesis and clinical characteristics must be improved for better treatment guidelines.
免疫疗法彻底改变了癌症治疗方式。包括靶向细胞毒性T淋巴细胞相关抗原4和程序性细胞死亡蛋白1的抗体在内的免疫检查点抑制剂已被证明在治疗某些类型的癌症方面有效。这些疗法的益处在于可延长转移性恶性肿瘤患者的预期寿命。风湿性不良事件并不常见。在本研究中,于2018年11月至2020年1月期间对9例患者进行了监测。肿瘤学家在患者接受免疫检查点抑制剂治疗后确定出现风湿毒性反应,并对患者进行了评估。仅纳入免疫治疗开始后出现风湿表现的肿瘤患者。毒性分级由肿瘤学家和风湿病学家共同进行,分级范围为1至5级(1级,轻度;2级,中度;3级,重度;4级,危及生命;5级,与毒性相关的死亡)。结果显示,每位患者采集的类风湿因子在所有病例中均为阴性。根据不良事件的严重程度,患者接受了非甾体抗炎药或泼尼松治疗。结果因不良事件的严重程度而异。总之,随着接受免疫检查点抑制剂治疗的患者数量增加,出现免疫相关不良事件(irAEs)的患者数量也会增加。肿瘤学家和风湿病学家之间应密切合作,以便为患者提供最佳治疗。免疫检查点抑制剂继发的肌肉骨骼表现与其他风湿性疾病略有不同,这使得诊断、治疗和监测都很困难。因此,免疫相关不良事件对肿瘤学家来说是新的且具有挑战性,必须提高对其发病机制和临床特征的认识,以制定更好的治疗指南。