Talamo G, Claxton D F, Dougherty D W, Ehmann C W, Sivik J, Drabick J J, Rybka W
Penn State Milton S Hershey Cancer Institute, Hershey, PA 17033-0850, USA.
Bone Marrow Transplant. 2009 Aug;44(3):157-61. doi: 10.1038/bmt.2008.446. Epub 2009 Feb 9.
High-dose melphalan is considered the current standard of care among the preparative regimens used in peripheral blood autologous SCT (ASCT) for multiple myeloma (MM). We report the results of a single ASCT in 79 MM patients using the BU/CY conditioning regimen, with BU 1 mg/kg p.o. or 0.8 mg/kg i.v. every 6 h x 16 doses, and CY 60 mg/kg per day i.v. for 2 days. ASCT was carried out in first (62%) or subsequent remission/refractory disease (38%). For an overall RR of 86%, 48 and 20 patients achieved PR and CR, respectively. At a median follow-up of 41 months (range 2-132 months), the estimated median OS and PFS were 45 months (95% confidence interval (CI)=38-92) and 20 months (95% CI=15-25), respectively. The BU/CY regimen was well tolerated, and transplant-related mortality was 4%. Clinical outcomes of the BU/CY regimen are not superior to those obtained in historical controls with high-dose melphalan followed by a single ASCT. Therefore, considering even the greater complexity of administration of the BU/CY regimen compared with that of single-agent melphalan, we believe the latter should remain the conditioning regimen of choice for ASCT in MM.
在用于多发性骨髓瘤(MM)外周血自体干细胞移植(ASCT)的预处理方案中,大剂量美法仑被认为是当前的标准治疗方法。我们报告了79例MM患者采用白消安/环磷酰胺(BU/CY)预处理方案进行单次ASCT的结果,其中白消安口服1mg/kg或静脉注射0.8mg/kg,每6小时1次,共16剂,环磷酰胺每天静脉注射60mg/kg,共2天。ASCT在首次缓解期(62%)或后续缓解期/难治性疾病期(38%)进行。总缓解率(RR)为86%,48例和20例患者分别达到部分缓解(PR)和完全缓解(CR)。中位随访41个月(范围2 - 132个月),估计中位总生存期(OS)和无进展生存期(PFS)分别为45个月(95%置信区间(CI)=38 - 92)和20个月(95%CI = 15 - 25)。BU/CY方案耐受性良好,移植相关死亡率为4%。BU/CY方案的临床结果并不优于既往采用大剂量美法仑后单次ASCT的对照结果。因此,考虑到与单药美法仑相比,BU/CY方案给药更为复杂,我们认为后者应仍然是MM患者ASCT的首选预处理方案。