首页> 外文期刊>Experimental Hematology: Official Publication of the International Society for Experimental Hematology >Post-transplant immunotherapy with donor-lymphocyte infusion and novel agents to upgrade partial into complete and molecular remission in allografted patients with multiple myeloma.
【24h】

Post-transplant immunotherapy with donor-lymphocyte infusion and novel agents to upgrade partial into complete and molecular remission in allografted patients with multiple myeloma.

机译:移植后免疫治疗,供体淋巴细胞输注和新型药物可将同种异体移植多发性骨髓瘤患者的部分缓解升级为完全缓解和分子缓解。

获取原文
获取原文并翻译 | 示例
           

摘要

OBJECTIVE: To investigate post-transplant immunotherapy with escalating donor-lymphocyte infusions (DLI) and novel agents (thalidomide, bortezomib, and lenalidomide) to target complete remission (CR). MATERIALS AND METHODS: Thirty-two patients with multiple myeloma who achieved only partial remission after allogeneic stem cell transplantation were treated with DLI. If no CR was achieved, one of the novel agents was added to target CR. RESULTS: CR defined either by European Group for Blood and Marrow Transplantation criteria, flow cytometry, or molecular methods as assessed by patient-specific immunoglobulin H-polymerase chain reaction or plasma cell chimerism polymerase chain reaction was accomplished in 59%, 63%, and 50% of patients, respectively. Achievement of CR resulted in improved 5-year progressive-free and overall survival, according to European Group for Blood and Marrow Transplantation criteria (53% vs 35%; p=0.03 and 90% vs 62%; p=0.06), flow cytometry (74% vs 15%; p=0.001 and 100% vs 52%; p=0.1), or molecular methods (84% vs 38%; p=0.001 and 100% vs 71%; p=0.03). CONCLUSIONS: Our finding demonstrates the clinical relevance of posttransplantation therapies to upgrade remission, and of remission's depth for long-term survival in myeloma patients.
机译:目的:研究移植后免疫疗法,以逐步提高的供体淋巴细胞输注(DLI)和新型药物(沙利度胺,硼替佐米和来那度胺)为靶点,以达到完全缓解(CR)的目的。材料与方法:异基因干细胞移植后仅获得部分缓解的32例多发性骨髓瘤患者接受DLI治疗。如果未实现CR,则将一种新型药物添加到目标CR中。结果:由欧洲血液和骨髓移植标准,流式细胞术或通过患者特异性免疫球蛋白H聚合酶链反应或浆细胞嵌合体聚合酶链反应评估的分子方法定义的CR的完成率分别为59%,63%和分别有50%的患者。根据欧洲血液和骨髓移植小组的标准(53%vs 35%; p = 0.03和90%vs 62%; p = 0.06),流式细胞术可以提高CR的获得率,从而改善5年无进展生存期和总生存期。 (74%vs 15%; p = 0.001和100%vs 52%; p = 0.1)或分子方法(84%vs 38%; p = 0.001和100%vs 71%; p = 0.03)。结论:我们的发现证明了骨髓瘤患者移植后治疗对改善缓解的临床意义以及缓解深度对长期生存的意义。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号