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Updated: Jun 16, 2026

Induction of Alloantigen-specific Anergy in Human Peripheral Blood Mononuclear Cells by Alloantigen Stimulation with Co-stimulatory Signal Blockade
Published on: March 14, 2011
Non-myeloablative conditioning and allogeneic transplantation for multiple myeloma
Keren Osman1, Brian Elliott, John Mandeli
1The Bone Marrow Transplant Program, The Mount Sinai Medical Center, New York, NY, USA. keren.osman@mountsinai.org
Nonmyeloablative allogeneic stem cell transplantation (NST) shows promise for relapsed/refractory multiple myeloma (MM). While transplant-related mortality was 25%, NST may offer survival benefits in select MM patients.
Area of Science:
- Hematology
- Oncology
- Stem Cell Transplantation
Background:
- Allogeneic stem cell transplantation (alloHCT) reduces relapse in multiple myeloma (MM) but has high mortality.
- Nonmyeloablative conditioning for allogeneic transplantation (NST) aims to decrease toxicity.
- NST efficacy is less established in relapsed/refractory MM compared to first remission.
Purpose of the Study:
- To evaluate the outcomes of NST in previously treated multiple myeloma patients.
- To assess transplant-related mortality, overall survival, and progression-free survival after NST.
- To identify patient factors influencing survival post-NST.
Main Methods:
- Retrospective analysis of 20 previously treated MM patients undergoing NST.
- Conditioning regimen included total body irradiation, antithymocyte globulin, and fludarabine.
- Immunosuppression with oral mycofenolate mofetil and cyclosporine was administered.
Main Results:
- 50% complete remission at day 100; 25% transplant-related mortality.
- Median overall survival (OS) was 21.2 months; 3-year OS was 24%.
- Median progression-free survival (PFS) was 6.6 months; 3-year PFS was 24%.
- Younger age (<52 years) and lower beta2 microglobulin (<2.5 mg/l) correlated with improved OS.
Conclusions:
- NST may offer a survival benefit for relapsed/refractory multiple myeloma.
- Younger age and favorable biomarkers predict better outcomes.
- Randomized trials are needed to confirm these findings and guide clinical practice.
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