Acquired lipodystrophy following use of pembrolizumab

Maya Weitzen , Marcus DaSilva Goncalves , Shaheer Khan , Alexander Barbaro , Richard Carvajal , Keyur Thakar
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Abstract

This case report details a 65-year-old female with Hashimoto's hypothyroidism and stage III melanoma who developed acquired generalized lipodystrophy (AGL), a rare immune-mediated adverse event, following pembrolizumab treatment. The patient was initially treated with nivolumab but was switched to pembrolizumab after developing optic neuritis. After starting pembrolizumab, the patient experienced significant weight loss and lipoatrophy in the face, thighs, and buttocks, alongside hypertrophy of the fat pads in her axillae, supraclavicular, and suprapubic areas. The patient also exhibited symptoms of marked insulin resistance and hypertriglyceridemia, indicative of AGL. Pembrolizumab treatment was discontinued after the patient developed additional side effects including hepatitis, hypophysitis, and thyroiditis, and the patient was commenced on steroid therapy. The patients insulin resistance and hypertriglyceridemia subsequently improved. Genetic sequencing excluded a genetic cause for her lipodystrophy. This is the fourth case of a patient developing AGL following administration of pembrolizumab, and the third for advanced melanoma. Since pembrolizumab administration for treatment of advanced melanoma is becoming more common, it necessitates clinician awareness to potential, rare complications not commonly defined in initial clinical trials.
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使用 Pembrolizumab 后获得性脂肪营养不良
本病例报告详细描述了一名患有桥本氏甲状腺功能减退症和黑色素瘤 III 期的 65 岁女性患者在接受 pembrolizumab 治疗后出现获得性全身脂肪营养不良(AGL)这一罕见的免疫介导不良事件。患者最初接受的是 nivolumab 治疗,但在出现视神经炎后改用了 pembrolizumab。开始使用 pembrolizumab 后,患者体重明显下降,脸部、大腿和臀部出现脂肪萎缩,腋窝、锁骨上和耻骨上区域的脂肪垫肥厚。患者还表现出明显的胰岛素抵抗症状和高甘油三酯血症,这表明她患有 AGL。在患者出现肝炎、肾上腺皮质功能减退症和甲状腺炎等其他副作用后,彭博利珠单抗治疗被中止,患者开始接受类固醇治疗。患者的胰岛素抵抗和高甘油三酯血症随后得到改善。基因测序排除了导致其脂肪营养不良的遗传原因。这是第四例服用 Pembrolizumab 后出现 AGL 的患者,也是第三例晚期黑色素瘤患者。由于使用 pembrolizumab 治疗晚期黑色素瘤越来越常见,因此临床医生有必要认识到潜在的罕见并发症,这些并发症在最初的临床试验中并不常见。
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CiteScore
0.40
自引率
0.00%
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0
审稿时长
96 days
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