Dasanu Constantin A, Alexandrescu Doru T
Department of Hematology-Oncology, Saint Francis Hospital and Medical Center, Hartford, CT, USA.
Eur J Haematol. 2009 Mar;82(3):231-4. doi: 10.1111/j.1600-0609.2008.01176.x. Epub 2008 Nov 6.
Lenalidomide is an important contemporary treatment option for patients with multiple myeloma (MM). Rare instances of autoimmune conditions have been observed in association with its use. Although moderate myelosuppression is not uncommonly seen in patients treated with lenalidomide, aplastic anemia has not previously been reported to be associated with this agent. We describe a case of severe aplastic anemia (AA) that was probably induced by lenalidomide. A 64-year-old male patient developed progressive pancytopenia three weeks into therapy with lenalidomide for his relapsed MM. A bone marrow aspirate and biopsy confirmed the diagnosis of AA and suggested the existence of an immunological reaction at the level of marrow. A gradual spontaneous recovery of normal hematopoiesis followed after the lenalidomide discontinuation.
来那度胺是多发性骨髓瘤(MM)患者重要的现代治疗选择。使用该药物时曾观察到罕见的自身免疫性疾病病例。虽然在接受来那度胺治疗的患者中,中度骨髓抑制并不少见,但此前尚未有报道称再生障碍性贫血与该药物有关。我们描述了一例可能由来那度胺诱发的严重再生障碍性贫血(AA)病例。一名64岁男性患者在使用来那度胺治疗复发MM三周后出现进行性全血细胞减少。骨髓穿刺和活检确诊为AA,并提示骨髓水平存在免疫反应。停用 来那度胺后,正常造血功能逐渐自发恢复。