Tandem autologous vs autologous plus reduced intensity allogeneic transplantation in the upfront management of multiple myeloma: meta-analysis of trials with biological assignment

被引:53
|
作者
Armeson, K. E. [1 ]
Hill, E. G. [1 ]
Costa, L. J. [2 ]
机构
[1] Med Univ S Carolina, Dept Med, Div Biostat & Epidemiol, Charleston, SC 29414 USA
[2] Med Univ S Carolina, Dept Med, Div Hematol & Med Oncol, Charleston, SC 29414 USA
关键词
meta-analysis; multiple myeloma; allogeneic transplantation; autologous transplantation; HLA; STEM-CELL TRANSPLANTATION; DONOR LYMPHOCYTE INFUSIONS; HIGH-DOSE THERAPY; TERM-FOLLOW-UP; MARROW-TRANSPLANTATION; STANDARD CHEMOTHERAPY; BONE-MARROW; BLOOD; IFM99-03; RESCUE;
D O I
10.1038/bmt.2012.173
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We utilized meta-analysis to compare tandem autologous (TA) hematopoietic SCT (auto-HSCT) or single auto-HSCT followed by reduced intensity conditioning (RIC), allogeneic (AR) hematopoietic SCT in the upfront management of patients with multiple myeloma (MM). A comprehensive search strategy of published and unpublished reports utilized the following entry criteria: newly diagnosed patients, first autologous transplantation in both arms, use of an RIC regimen and assignment to TA or AR based exclusively on the availability of an HLA matched donor. Six trials were identified yielding 1192 subjects in TA and 630 in AR. Patients in AR had higher likelihoods of TRM (relative risk (RR) = 3.3, 95% confidence interval (CI) = 2.2-4.8) and CR (RR = 1.4, 95% CI = 1.1-1.8). OS was not different in the first 36 months (hazard ratio (HR) = 1.15, 95% CI = 0.91-1.45) or after (HR = 0.74, 95% CI = 0.53-1.04) 36 months from assignment. Similar findings were seen for PFS. When compared with TA in the upfront management of MM, AR is associated with higher TRM and CR without improvement in PFS or OS. Bone Marrow Transplantation (2013) 48, 562-567; doi: 10.1038/bmt.2012.173; published online 10 September 2012
引用
收藏
页码:562 / 567
页数:6
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