Department of General Surgery, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu 210001, P.R. China.
Department of General Surgery, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu 210001, P.R. China.
Int J Oncol. 2022 Jun;60(6). doi: 10.3892/ijo.2022.5364. Epub 2022 Apr 29.
In 2020, there were an estimated 19.3 million new cancer cases and close to 10 million cancer deaths worldwide. Cancer remains one of the leading causes of death. In recent years, with the continuous improvement of our understanding of tumor immunotherapy, immunotherapeutics, such as immune checkpoint inhibitors, have gradually become a hot spot for tumor treatment. Amongst these, programmed cell death protein 1/programmed cell death protein ligand 1 (PD‑1/PD‑L1) related inhibitors, such as nivolumab and pembrolizumab, atezolizumab, avelumab and durvalumab have been shown to exhibit a high level of efficacy in several types of tumors. It has been confirmed that these inhibitors play an important role in the anti‑tumor process, significantly improving the survival rate of patients and delaying the progress of the underlying cancer. However, its method of therapeutic interference and potential for damaging the immune system has caused concern regarding its suitability. As these adverse effects are caused by an immune response to endogenous tissues, they are designated as immune‑related adverse events (irAEs). In this review, the typical irAEs reported in recent years and the management strategies adopted are highlighted, to serve as a reference in assessing the clinical response to these adverse reactions.
2020 年,全球估计有 1930 万例新癌症病例和近 1000 万癌症死亡病例。癌症仍然是主要死亡原因之一。近年来,随着我们对肿瘤免疫治疗的不断深入了解,免疫疗法,如免疫检查点抑制剂,逐渐成为肿瘤治疗的热点。在这些免疫疗法中,程序性细胞死亡蛋白 1/程序性细胞死亡蛋白配体 1(PD-1/PD-L1)相关抑制剂,如 nivolumab 和 pembrolizumab、atezolizumab、avelumab 和 durvalumab,已被证明在几种类型的肿瘤中具有很高的疗效。已经证实,这些抑制剂在抗肿瘤过程中发挥着重要作用,显著提高了患者的生存率并延缓了癌症的进展。然而,其治疗干扰方法及其对免疫系统造成损害的潜力引起了人们对其适用性的关注。由于这些不良反应是由对内源性组织的免疫反应引起的,因此将其指定为免疫相关不良反应(irAEs)。在这篇综述中,强调了近年来报告的典型 irAEs 及其采用的管理策略,为评估这些不良反应的临床反应提供参考。