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Clinical Trial Summary

The clinical trial was conducted in a cohort of young, high-risk myeloma patients who were designed to receive a combination of high-dose chemotherapy with allogeneic or autologous hematopoietic stem cell transplantation. The objective was to assess the progression free survival (PFS), overall survival (OS),and overall response rate (ORR) of the overall treatment.


Clinical Trial Description

50 cases of HR-NDMM patients were divided into two groups nonrandomizedly. TE group received hematopoietic stem cell transplantation after induction therapy. Allo-sct for the young patients with suitable donors, Asct for the others. TNE group received consolidation therapy after induction therapy. All patients received PI-based maintenance therapy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04008888
Study type Interventional
Source Institute of Hematology & Blood Diseases Hospital
Contact WEI W SUI, Dr.
Phone 86-022-23909171
Email suiweiwei@ihcams.ac.cn
Status Recruiting
Phase N/A
Start date January 5, 2018
Completion date August 1, 2020

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