Bashey Asad, Pérez Waleska S, Zhang Mei-Jie, Anderson Kenneth C, Ballen Karen, Berenson James R, To L Bik, Fonseca Rafael, Freytes César O, Gale Robert Peter, Gibson John, Giralt Sergio A, Kyle Robert A, Lazarus Hillard M, Maharaj Dipnarine, McCarthy Philip L, Milone Gustavo A, Nimer Stephen, Pavlovsky Santiago, Reece Donna E, Schiller Gary, Vesole David H, Hari Parameswaran
BMT Group of Georgia, Atlanta, Georgia.
Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
Biol Blood Marrow Transplant. 2008 Oct;14(10):1118-1124. doi: 10.1016/j.bbmt.2008.07.007.
Relapse is the overwhelming cause of treatment failure after autologous transplantation for multiple myeloma (MM). For patients with a syngeneic donor, twin transplants provide a healthy graft that is free of myeloma. The relative impact of the graft on posttransplant relapse can be estimated by comparing risk of relapse after hematopoietic cell transplantation from genetically identical twins versus autotransplants because confounding differences in minor or major histocompatibility antigens are absent in the syngeneic transplant setting. Outcomes of 43 subjects who received twin transplants for MM were compared to 170 matched autotransplant recipients reported to the Center for International Blood and Marrow Transplant Research (CIBMTR). Multivariate analysis was performed by fitting a Cox model stratified on matched pairs. The matched transplant patients studied were similar with respect to subject-, disease-, and transplant-related characteristics. Cumulative incidence of relapse/progression was significantly lower, and progression-free survival (PFS) was significantly higher following twin transplants. In multivariate analysis, the probability of relapse/progression was lower in twins (relative risk [RR] = 0.49, 95% confidence interval [CI] 0.28-0.86, P = .011). Twin transplants have a significantly lower relapse risk than autotransplants in MM, suggesting that graft composition may impact outcomes following high-dose chemotherapy.
复发是多发性骨髓瘤(MM)自体移植后治疗失败的主要原因。对于有同基因供体的患者,双胞胎移植可提供无骨髓瘤的健康移植物。通过比较来自基因相同双胞胎的造血细胞移植与自体移植后复发风险,可评估移植物对移植后复发的相对影响,因为在同基因移植环境中不存在次要或主要组织相容性抗原的混杂差异。将43例接受MM双胞胎移植的受试者的结果与向国际血液和骨髓移植研究中心(CIBMTR)报告的170例匹配自体移植受者的结果进行比较。通过拟合按匹配对分层的Cox模型进行多变量分析。所研究的匹配移植患者在受试者、疾病和移植相关特征方面相似。双胞胎移植后复发/进展的累积发生率显著更低,无进展生存期(PFS)显著更长。在多变量分析中,双胞胎复发/进展的概率更低(相对风险[RR]=0.49,95%置信区间[CI]0.28 - 0.86,P = 0.011)。在MM中,双胞胎移植的复发风险显著低于自体移植,这表明移植物组成可能影响大剂量化疗后的结果。