Alexanian R, Barlogie B, Tucker S
University of Texas, M.D. Anderson Cancer Center, Houston 77030.
Am J Hematol. 1990 Feb;33(2):86-9. doi: 10.1002/ajh.2830330203.
An alternating VCAD-VAD regimen, combining vincristine-doxorubicin by continuous infusion with cyclophosphamide and pulse dexamethasone, or VAD alone, was given to 175 previously untreated patients with multiple myeloma. The response rate with primary VAD-based regimens of 55% was virtually identical to the 54% in comparable patients treated previously with similar programs by using bolus vincristine-doxorubicin. Despite responses to VAD that were more rapid in onset than any previous treatment, remission and survival times were similar. This may be due to major differences in drug sensitivity between progenitor and differentiated plasma cells. A VAD-based regimen seems better for newly diagnosed patients when rapid control of multiple myeloma is necessary.
对175例未经治疗的多发性骨髓瘤患者采用交替的VCAD-VAD方案,即持续输注长春新碱-阿霉素联合环磷酰胺和脉冲地塞米松,或单独使用VAD方案。以VAD为主的初始方案的缓解率为55%,与之前使用大剂量长春新碱-阿霉素的类似方案治疗的可比患者的54%几乎相同。尽管VAD治疗的起效比以往任何治疗都更快,但缓解期和生存期相似。这可能是由于祖细胞和分化浆细胞之间药物敏感性的重大差异。当需要快速控制多发性骨髓瘤时,基于VAD的方案对新诊断患者似乎更好。