Demichelis Chiara, Balestra Andrea, Lapucci Caterina, Zuppa Angela, Grisanti Stefano G, Prada Valeria, Pesce Giampaola, Grasso Ilaria, Queirolo Paola, Schenone Angelo, Benedetti Luana, Grandis Marina
Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Neurol Sci. 2021 Apr;42(4):1405-1409. doi: 10.1007/s10072-020-04604-1. Epub 2020 Aug 11.
In the last years, many new drugs have been developed targeting different oncology pathways, overall improving both quality of life and survival in several malignancies. However, the increase of those therapies is associated with novel toxicities, mainly immune-related adverse events (irAEs), never observed before. Different irAEs are now well characterized, and, among them, neuromuscular complications, following immune checkpoint inhibitor (ICPi) therapy, are increasingly studied and described. However, there are also neurological complications related to the use of other targeted therapies, less known and probably underestimated. Herein we describe two oncological patients who developed neuromuscular diseases after administration of targeted therapies, different from ICPi.
The first patient was treated with the combination of Vemurafenib and Cobimetinib, BRAF and MEK inhibitors, respectively, for a cutaneous melanoma. One year after the beginning of the combined treatment, she developed a sub-acute motor neuropathy with predominant cranial nerve involvement. She was successfully treated with methylprednisolone. The second patient received therapy with Imatinib, tyrosine kinase inhibitor and precursor of the targeted therapy, for a gastrointestinal stromal tumour. Few days after the first administration, he developed generalized myasthenia gravis with respiratory failure. Clinical remission was obtained with plasma-exchange, intravenous immunoglobulins and steroids. DISCUSSION AND CONCLUSION: We strengthen the relevance of neuromuscular complications which may occur long after treatment start or in patients receiving not only the latest ICPi but also "older" and apparently better-known targeted therapies. Also in the latter cases, an immune-mediated "off-target" pathogenic mechanism can be hypothesized, and consequences can be life threatening, if not promptly diagnosed and appropriately managed.
在过去几年中,已经开发出许多针对不同肿瘤学途径的新药,总体上改善了几种恶性肿瘤患者的生活质量和生存率。然而,这些治疗方法的增加与新的毒性相关,主要是免疫相关不良事件(irAEs),这是以前从未观察到的。现在不同的irAEs已得到很好的表征,其中,免疫检查点抑制剂(ICPi)治疗后的神经肌肉并发症越来越受到研究和描述。然而,使用其他靶向治疗也会出现神经并发症,这些并发症鲜为人知且可能被低估。在此,我们描述了两名肿瘤患者,他们在接受不同于ICPi的靶向治疗后发生了神经肌肉疾病。
首例患者因皮肤黑色素瘤接受了分别为BRAF和MEK抑制剂的维莫非尼和考比替尼联合治疗。联合治疗开始一年后,她出现了以颅神经受累为主的亚急性运动神经病。她接受甲泼尼龙治疗后康复。第二例患者因胃肠道间质瘤接受了酪氨酸激酶抑制剂伊马替尼(靶向治疗的前身)治疗。首次给药后几天,他出现了伴有呼吸衰竭的全身重症肌无力。通过血浆置换、静脉注射免疫球蛋白和类固醇治疗获得了临床缓解。
我们强调了神经肌肉并发症的相关性,这些并发症可能在治疗开始后很长时间出现,或者发生在不仅接受最新ICPi治疗,还接受“较旧”且看似更知名靶向治疗的患者中。在后一种情况下,也可以假设存在免疫介导的“脱靶”致病机制,如果不及时诊断和适当处理,后果可能危及生命。