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Updated: Jun 15, 2026

Intrafemoral Injection of Human Hematopoietic Stem and Progenitor Cells into Immunocompromised Mice
Published on: December 8, 2023
Hematopoietic stem cell transplantation for multiple myeloma beyond 2010
Joan Bladé1, Laura Rosiñol, Maria Teresa Cibeira
1Department of Hematology and Bone Marrow Transplant Unit, Institut of Hematology and Oncology, Hospital Clinic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Spain. jblade@clinic.ub.es
Autologous stem cell transplantation (ASCT) improves outcomes for multiple myeloma patients. Novel agents enhance complete remission rates, suggesting high-dose therapy optimization is key.
Area of Science:
- Hematology
- Oncology
- Stem Cell Transplantation
Background:
- Autologous stem cell transplantation (ASCT) is the standard frontline therapy for younger multiple myeloma patients, offering superior complete remission (CR) and event-free survival compared to chemotherapy.
- Achieving CR post-ASCT is crucial for patient benefit, with M-protein levels pre-transplant influencing CR likelihood.
Purpose of the Study:
- To evaluate the impact of novel agents on ASCT outcomes in multiple myeloma.
- To assess the role of optimized high-dose therapy in the era of novel agents.
- To review the advancements in allogeneic transplantation strategies for multiple myeloma.
Main Methods:
- Analysis of outcomes data for multiple myeloma patients undergoing ASCT with novel agent incorporation.
- Review of studies on reduced-intensity conditioning allogeneic transplantation.
- Evaluation of post-transplantation consolidation and maintenance strategies.
Main Results:
- Novel agents increase pre- and post-transplant CR rates, with bortezomib-containing regimens showing promise in poor-risk cytogenetics.
- Reduced-intensity conditioning allogeneic transplantation shows a progression-free survival plateau of 25-30% beyond 6 years.
- Post-transplant consolidation/maintenance with new drugs yields encouraging results.
Conclusions:
- High-dose therapy should be optimized, not replaced, in the era of novel agents for multiple myeloma.
- Reduced-intensity conditioning allogeneic transplantation is a viable option, with ongoing research focused on preparative regimens and GVHD/graft-versus-myeloma strategies.
- Further follow-up is needed to confirm the long-term survival impact of increased CR rates achieved with novel agents.
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