沙利度胺联合地塞米松有效治疗原发性浆细胞白血病1例。

Stefan Wöhrer, Jutta Ackermann, Catrin Baldia, Sonja Seidl, Markus Raderer, Ingrid Simonitsch, Johannes Drach
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引用次数: 18

摘要

浆细胞白血病(PCL)是一种侵袭性疾病,预后差,中位生存期仅为2-6个月。目前,尚无标准的治疗方法,但强化综合化疗似乎比传统的美法兰加强的松更有效。然而,沙利度胺在PCL中的疗效尚未得到广泛评价。最近,据报道,沙利度胺治疗难治性多发性骨髓瘤取得了令人鼓舞的结果。在这里,我们报告了一位原发性PCL患者,他在一线使用沙利度胺/地塞米松治疗后迅速反应,并取得了非常好的部分缓解。
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Effective treatment of primary plasma cell leukemia with thalidomide and dexamethasone - a case report.

Plasma cell leukemia (PCL) is an aggressive disease with poor prognosis and a median survival of only 2-6 months. Currently, no standard therapy is available, but intensive polychemotherapy appears to be more effective than the conventional melphalan plus prednisone. However, the efficacy of thalidomide in PCL has not yet been widely evaluated. Recently, treatment with thalidomide has been reported to yield promising results in refractory multiple myeloma. Here, we report on a patient with primary PCL in whom first-line treatment with thalidomide/dexamethasone resulted in a rapid response and achievement of a very good partial remission.

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