Coates Stephanie, Barker Alan, Spurgeon Stephen
Division of Pulmonary and Critical Care Medicine, Oregon Health and Science University, Portland, OR 97239, USA.
J Oncol Pharm Pract. 2012 Jun;18(2):284-6. doi: 10.1177/1078155211408374. Epub 2011 Jul 8.
Lenalidomide is a derivative of thalidomide and is FDA-approved for the treatment of myelodysplastic syndrome and, in combination with dexamethasone, for the treatment of relapsed multiple myeloma. Pulmonary toxicity with thalidomide is a recognized potential complication; however, there have only been two case reports in the literature of lenalidomide-associated pulmonary toxicity. In this case, we describe a patient who developed profound dyspnea, decreased exercisetolerance, and new ground-glass opacities with reticulation, consistent with a nonspecific interstitial pneumonia pattern. Clinical suspicion for pulmonary drug toxicity was high and lenalidomide was discontinued. Within 2 weeks of stopping lenalidomide, the patient had significant improvement in dyspnea and interstitial changes on CT were resolving. After 8 weeks, there was complete resolution of symptoms. Lenalidomide-induced pulmonary toxicity is significantly debilitating but, to date, it appears to be reversible with discontinuation of the medication.
来那度胺是沙利度胺的衍生物,已获美国食品药品监督管理局(FDA)批准用于治疗骨髓增生异常综合征,以及与地塞米松联合用于治疗复发的多发性骨髓瘤。沙利度胺所致的肺部毒性是一种公认的潜在并发症;然而,文献中仅有两例来那度胺相关肺部毒性的病例报告。在此病例中,我们描述了一名患者,该患者出现严重呼吸困难、运动耐量下降,以及新出现的伴有网状影的磨玻璃样混浊,符合非特异性间质性肺炎的表现。临床高度怀疑肺部药物毒性,遂停用了来那度胺。在停用来那度胺的2周内,患者的呼吸困难有显著改善,CT上的间质性改变也在逐渐消退。8周后,症状完全消失。来那度胺所致的肺部毒性会严重损害身体,但迄今为止,停药后似乎是可逆的。