Barton James C
Department of Medicine, Brookwood Medical Center, Birmingham, Alabama, USA.
Am J Hematol. 2003 Nov;74(3):205-7. doi: 10.1002/ajh.10416.
A 67-year-old woman with previously untreated lambda-positive B-chronic lymphocytic leukemia (CLL) had kappa-positive myeloma develop that was treated with daily thalidomide and intermittent dexamethasone. After 4 months, there was a marked reduction in marrow plasmacytosis, urine kappa chains, and peripheral blood and marrow lymphocytosis. She reduced her thalidomide (but not dexamethasone) doses after 6 months, because she had symptoms of peripheral neuropathy. Although blood lymphocyte concentrations remained normal, she had progression of myeloma and died. Thalidomide and dexamethasone therapy similar to that administered for myeloma alone may be effective treatment for myeloma in patients with preexisting B-CLL and may also have anti-B-CLL activity.
一名67岁、既往未经治疗的λ阳性B细胞慢性淋巴细胞白血病(CLL)女性患者发生了κ阳性骨髓瘤,接受了沙利度胺每日治疗及地塞米松间歇治疗。4个月后,骨髓浆细胞增多、尿κ链以及外周血和骨髓淋巴细胞增多均显著减轻。6个月后,她因出现周围神经病变症状而减少了沙利度胺(而非地塞米松)的剂量。尽管血液淋巴细胞浓度仍保持正常,但她的骨髓瘤病情进展,最终死亡。与单独用于骨髓瘤治疗类似的沙利度胺和地塞米松联合疗法,可能是既往存在B-CLL患者骨髓瘤的有效治疗方法,并且可能也具有抗B-CLL活性。