Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Pulmonary Division, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; Department of Medicine, Weill Cornell Medical Center, New York, New York.
J Thorac Oncol. 2021 Oct;16(10):1759-1764. doi: 10.1016/j.jtho.2021.06.024. Epub 2021 Jul 12.
The optimal management for immune-related adverse events (irAEs) in patients who do not respond or become intolerant to steroids is unclear. Guidelines suggest additional immunosuppressants on the basis of case reports and expert opinion.
We evaluated patients with lung cancers at Memorial Sloan Kettering Cancer Center treated with immune checkpoint blockade from 2011 to 2020. Pharmacy records were queried to identify patients who received systemic steroids and an additional immunosuppressant (e.g., tumor necrosis factor-α inhibitor, mycophenolate mofetil). Patient records were manually reviewed to evaluate baseline characteristics, management, and outcomes.
Among 2750 patients with lung cancers treated with immune checkpoint blockade, 51 (2%) received both steroids and an additional immunosuppressant for a severe irAE (tumor necrosis factor-α inhibitor (73%), mycophenolate mofetil (20%)). The most common events were colitis (53%), pneumonitis (20%), hepatitis (12%), and neuromuscular (10%). At 90 days after the start of an additional immunosuppressant, 57% were improved from their irAE, 18% were unchanged, and 25% were deceased. Improvement was more common in hepatitis (five of six) and colitis (18 of 27) but less common in neuromuscular (one of five) and pneumonitis (3 of 10). Of the patients who died, 8 of 13 were attributable directly to the irAE and 4 of 13 were related to toxicity from immunosuppression (three infection-related deaths, one drug-induced liver injury leading to acute liver failure).
Steroid-refractory or resistant irAEs events are rare. Although existing treatments help patients with hepatitis and colitis, many patients with other irAEs remain refractory or experience toxicities from immunosuppression. A more precise understanding of the pathophysiology of specific irAEs is needed to guide biologically-informed treatments for severe irAEs.
对于对类固醇无反应或不耐受的患者,免疫相关不良事件(irAE)的最佳治疗方法尚不清楚。指南基于病例报告和专家意见建议使用其他免疫抑制剂。
我们评估了 2011 年至 2020 年在纪念斯隆凯特琳癌症中心接受免疫检查点阻断治疗的肺癌患者。通过药房记录确定接受全身皮质类固醇和其他免疫抑制剂(例如肿瘤坏死因子-α抑制剂、霉酚酸酯)治疗的患者。通过手动审查患者记录来评估基线特征、治疗和结局。
在接受免疫检查点阻断治疗的 2750 例肺癌患者中,51 例(2%)因严重 irAE(肿瘤坏死因子-α抑制剂(73%)、霉酚酸酯(20%))同时接受皮质类固醇和其他免疫抑制剂治疗。最常见的事件是结肠炎(53%)、肺炎(20%)、肝炎(12%)和神经肌肉疾病(10%)。在开始使用其他免疫抑制剂后 90 天,57%的患者 irAE 得到改善,18%的患者无变化,25%的患者死亡。在肝炎(五例中的六例)和结肠炎(二十七例中的十八例)中,改善更为常见,但在神经肌肉疾病(五例中的一例)和肺炎(十例中的三例)中则不常见。在死亡的患者中,13 例中有 8 例直接归因于 irAE,13 例中有 4 例与免疫抑制毒性相关(三例感染相关死亡,一例药物性肝损伤导致急性肝衰竭)。
类固醇难治性或耐药性 irAE 事件很少见。尽管现有治疗方法可帮助患有肝炎和结肠炎的患者,但许多患有其他 irAE 的患者仍对治疗无反应或因免疫抑制而出现毒性。需要更深入地了解特定 irAE 的病理生理学,以指导针对严重 irAE 的基于生物学的治疗方法。