Williams Sarah, Liang Christina, Guminski Alexander, Hruby George, Chan David
Medical Oncology Department, Royal North Shore Hospital, Reserve Rd, St Leonards, NSW 2065, Australia.
Neurology, Royal North Shore Hospital, St. Leonards, NSW, Australia.
Oxf Med Case Reports. 2022 Feb 19;2022(2):omac012. doi: 10.1093/omcr/omac012. eCollection 2022 Feb.
We report on a 79-year-old man diagnosed with localized Merkel cell carcinoma (MCC) who also had acetylcholine receptor antibody (Ach-R-Ab)-positive myasthenia gravis (MG) controlled on prednisolone, mycophenolate and intravenous immunoglobulin (IVIG). His MCC was initially treated with radiation, followed by chemotherapy on metastatic recurrence. Chemotherapy initially stabilized the disease, but he experienced significant fatigue and his disease progressed within 3 months. After careful consideration of the risk of a myasthenic crisis, he was commenced on avelumab. He had initial partial response, though he ultimately developed progressive disease which led to a decision for best supportive care at 10 months post starting immunotherapy. Importantly, as per spirometry, his MG remained stable throughout immunotherapy. We present the current case to demonstrate that MG should not be viewed as an absolute contraindication to immunotherapy in scenarios where there are limited alternate therapeutic options.
我们报告了一名79岁男性,被诊断为局限性默克尔细胞癌(MCC),同时患有乙酰胆碱受体抗体(Ach-R-Ab)阳性重症肌无力(MG),通过泼尼松龙、霉酚酸酯和静脉注射免疫球蛋白(IVIG)进行控制。他的MCC最初接受放射治疗,转移性复发后接受化疗。化疗最初使病情稳定,但他出现了严重疲劳,且疾病在3个月内进展。在仔细考虑重症肌无力危象的风险后,他开始使用阿维鲁单抗治疗。他最初有部分缓解,尽管最终疾病进展,在开始免疫治疗10个月后决定给予最佳支持治疗。重要的是,根据肺活量测定,他的MG在整个免疫治疗过程中保持稳定。我们展示当前病例以证明,在替代治疗选择有限的情况下,MG不应被视为免疫治疗的绝对禁忌证。