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Lambert-Eaton Myasthenic Syndrome Secondary to Nivolumab and Ipilimumab in a Patient with Small-Cell Lung Cancer

机译:小细胞肺癌患者继发于Nivolumab和Ipilimumab的Lambert-Eaton重症肌无力综合征

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摘要

We present a case of a 59-year-old male with a confirmed diagnosis of small-cell lung cancer (SCLC). He had progressive disease even after four cycles of cisplatin and etoposide chemotherapy and 21 cycles of radiation. He was therefore started on immunotherapy with nivolumab every 2 weeks and ipilimumab every 6 weeks. After 4 months of starting immunotherapy, he reported extreme fatigue, muscular weakness, and poor appetite. He was diagnosed with hypothyroidism, primary adrenal insufficiency, and Lambert-Eaton Myasthenic Syndrome (LEMS). LEMS can be both a paraneoplastic syndrome of SCLC and an adverse effect of immunotherapy. Currently, there is no diagnostic test available to determine if a case of LEMS is a paraneoplastic syndrome or immunotherapy-related adverse effect. In our patient, we felt that LEMS was an immunotherapy-related adverse effect rather being a paraneoplastic syndrome. Our determination was based on the time of onset of muscular weakness, presence of other immunotherapy-mediated adverse events, and the appearance of symptoms in spite of SCLC that had been stabilized on immunotherapy. Accordingly, immunotherapy was stopped and a brief tapering course of steroids was initiated. Our patient's muscular weakness from LEMS responded well. His clinical improvement persisted even with radiologic progression of disease after cessation of immunotherapy.
机译:我们介绍了一例确诊为小细胞肺癌(SCLC)的59岁男性。即使进行了四个周期的顺铂和依托泊苷化疗和21个放射周期,他仍患有疾病。因此,他开始每2周进行一次nivolumab免疫治疗,每6周进行一次ipilimumab免疫治疗。开始免疫治疗4个月后,他报告出现极度疲劳,肌肉无力和食欲不振。他被诊断患有甲状腺功能减退,原发性肾上腺皮质功能不全和兰伯特-伊顿肌无力综合症(LEMS)。 LEMS既可以是SCLC的副肿瘤综合征,也可以是免疫治疗的不良反应。当前,没有可用的诊断测试来确定LEMS病例是副肿瘤综合症还是免疫治疗相关的不良反应。在我们的患者中,我们认为LEMS是与免疫治疗相关的不良反应,而不是副肿瘤综合征。我们的确定是基于肌肉无力发作的时间,其他免疫疗法介导的不良事件的出现以及尽管在免疫疗法上已稳定的SCLC症状的出现。因此,停止了免疫治疗并开始了短暂的类固醇逐渐减少过程。 LEMS患者的肌肉无力反应良好。即使在停止免疫治疗后,即使疾病的放射学进展,他的临床改善仍然持续。

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