Fu Chengcheng, Wang Juan, Xin Xue, Liu Hui, Xue Shengli, Ma Xiao, Jin Zhengming, Sun Aining, Qiu Huiying, Wu Depei
Jiangsu Institute of Hematology, Key Laboratory of Thrombosis and Hemostasis, Ministry of Health, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, P.R. China.
Exp Ther Med. 2013 Oct;6(4):977-982. doi: 10.3892/etm.2013.1261. Epub 2013 Aug 16.
The present study aimed to evaluate the effect of autologous hematopoietic stem cell transplantation (ASCT) on the response and outcome of patients with multiple myeloma (MM) and to analyze the factors influencing the prognosis of the disease. Retrospective analysis was performed in 27 patients with MM who had been treated by ASCT (ASCT group) and 28 patients treated with combined chemotherapy only (non-ASCT group) from May 2004 to August 2011. The impact on the depth of response, progression-free survival (PFS) and overall survival (OS) times, as well as associated prognostic factors of patients with MM, were analyzed. All patients successfully underwent hematopoietic reconstruction without transplantation-related mortality. The complete remission (CR) rate of patients in the ASCT group significantly increased from 25.9% (7/27) before ASCT to 70.4% (19/27) following ASCT (P<0.01). The probability of OS for 5 years was 52.2% for the patients in the ASCT group and 33.1% for those in the non-ASCT group (P>0.05). Univariate analysis in the ASCT group demonstrated that maintenance and consolidation therapies were associated with significant increases in PFS (P=0.01) and OS (P<0.01) times. The present study demonstrated that ASCT further increases the CR rate, prolongs PFS time and potentially increases the OS time. Incorporation of these novel agents, including the protea-some inhibitor bortezomib and the immunomodulatory drugs thalidomide and lenalidomide, into the induction, consolidation and maintenance phases has optimized the anti-myeloma activity of ASCT.
本研究旨在评估自体造血干细胞移植(ASCT)对多发性骨髓瘤(MM)患者缓解情况及预后的影响,并分析影响该疾病预后的因素。对2004年5月至2011年8月期间接受ASCT治疗的27例MM患者(ASCT组)和仅接受联合化疗的28例患者(非ASCT组)进行回顾性分析。分析了其对MM患者缓解深度、无进展生存期(PFS)和总生存期(OS)的影响以及相关预后因素。所有患者均成功实现造血重建,无移植相关死亡。ASCT组患者的完全缓解(CR)率从ASCT前的25.9%(7/27)显著提高至ASCT后的70.4%(19/27)(P<0.01)。ASCT组患者5年OS概率为52.2%,非ASCT组为33.1%(P>0.05)。ASCT组的单因素分析表明,维持和巩固治疗与PFS(P=0.01)和OS(P<0.01)时间的显著延长相关。本研究表明,ASCT进一步提高了CR率,延长了PFS时间,并可能延长OS时间。将这些新型药物,包括蛋白酶体抑制剂硼替佐米以及免疫调节药物沙利度胺和来那度胺,纳入诱导、巩固和维持阶段,优化了ASCT的抗骨髓瘤活性。