CHA University, School of Medicine, Seongnam, Korea.
Hematology and Oncology, Department of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, Korea.
Medicine (Baltimore). 2022 Sep 9;101(36):e30236. doi: 10.1097/MD.0000000000030236.
The indications for immune checkpoint inhibitors (ICIs) are expanding for various cancers because of their durable responses and tolerable safety profiles. Immune-related adverse events (irAEs), including neurological adverse events (nAEs), are associated with ICIs therapy. However, there have been few studies on whether re-challenge with ICIs can be clinically acceptable after neurological AE has improved.
A 69-year-old woman with recurrent ovarian cancer undergoing palliative chemotherapy was admitted to our hospital with sudden development of diplopia, dizziness, and gait instability. The patient was administered ICI therapy with anti-angiogenic agents for 9 weeks for 3 cycles.
We performed neurological examination, brain imaging, nerve conduction studies, and serology tests. The patient was diagnosed with Guillain-Barré syndrome variant, an immune-mediated polyneuropathy characterized by a triad of ataxia, areflexia, and ophthalmoplegia.
After prompt discontinuation of pembrolizumab, the patient was taken intravenous methylprednisolone (2 mg/kg) was administered for 5 days, and her symptoms were partially resolved. With the addition of immunoglobulin 0.4 g/kg for 5 days, her symptoms gradually improved.
The patient's neurological symptoms improved after immunosuppressive therapy, without sequelae. The NCV showed normal nerve conduction. Unfortunately, because there was little evidence for pembrolizumab rechallenge, pembrolizumab therapy was permanently discontinued, and the tumors eventually progressed.
由于免疫检查点抑制剂 (ICI) 的持久反应和可耐受的安全性,其适应证正在不断扩大,适用于各种癌症。免疫相关不良事件 (irAE),包括神经不良事件 (nAE),与 ICI 治疗相关。然而,关于 nAE 改善后是否可以重新使用 ICI 进行临床治疗,目前研究较少。
一名 69 岁女性,患有复发性卵巢癌,正在接受姑息性化疗,因突发复视、头晕和步态不稳而被收入我院。该患者因 3 个周期共 9 周接受了抗血管生成药物的 ICI 治疗。
我们进行了神经科检查、脑部成像、神经传导研究和血清学检查。该患者被诊断为吉兰-巴雷综合征变异型,这是一种免疫介导的多神经病,其特征为共济失调、反射消失和眼肌瘫痪三联征。
在迅速停用 pembrolizumab 后,患者接受了 5 天 2mg/kg 的甲基泼尼松龙静脉注射治疗,症状部分缓解。加用免疫球蛋白 0.4g/kg 治疗 5 天后,症状逐渐改善。
患者的神经症状在免疫抑制治疗后得到改善,无后遗症。NCV 显示正常的神经传导。不幸的是,由于缺乏 pembrolizumab 再挑战的证据,永久性停止了 pembrolizumab 治疗,肿瘤最终进展。