Hussein Mohamad A
Cleveland Clinic Multidisciplinary Multiple Myeloma Research Program, Cleveland, OH 44195, USA. mah+
Expert Rev Anticancer Ther. 2005 Feb;5(1):25-31. doi: 10.1586/14737140.5.1.25.
Multiple myeloma continues to be an incurable disease. The understanding of the disease's pathophysiology has significantly improved over the past few years, partly due to the discovery of the role of immunomodulatory agents and the study of their mechanism of action. Thalidomide, the first of the immunomodulatory family to be used in the management of multiple myeloma, proved not only to be effective in the treatment of multiple myeloma, but also instigated a wide range of in vitro and in vivo studies to define the pathophysiology of the plasma cell dyscrasia. The attention thalidomide has received in the past and recent history has not been without a price. The drug has a side-effect profile that, if managed appropriately, provides the most unique active molecule in the management of the disease, where it maintains the same response rate in newly diagnosed patients as in advanced relapsed/refractory multiple myeloma patients.
多发性骨髓瘤仍然是一种无法治愈的疾病。在过去几年中,对该疾病病理生理学的理解有了显著提高,部分原因是免疫调节剂作用的发现及其作用机制的研究。沙利度胺是免疫调节家族中首个用于治疗多发性骨髓瘤的药物,它不仅被证明对多发性骨髓瘤的治疗有效,还引发了广泛的体外和体内研究,以明确浆细胞发育异常的病理生理学。沙利度胺在过去和近期受到的关注并非没有代价。该药物具有一些副作用,如果管理得当,它是治疗该疾病最独特的活性分子,在新诊断患者中的缓解率与晚期复发/难治性多发性骨髓瘤患者相同。