Abstract
Systemic light chain (AL) amyloidosis is a rare protein misfolding and deposition disorder. Clonal plasma cells or rarely B cells produce immunoglobulin light chains with the potential to misfold. Treatment is clone directed with the goal to achieve a complete or at least very good hematological remission. AutoHCT is an option in a selected group of patients. Results from cellular therapies are encouraging and will play an important role in the future.
| Original language | English |
|---|---|
| Title of host publication | The EBMT Handbook |
| Subtitle of host publication | Hematopoietic Cell Transplantation and Cellular Therapies |
| Publisher | Springer |
| Pages | 751-755 |
| Number of pages | 5 |
| ISBN (Electronic) | 9783031440809 |
| ISBN (Print) | 9783031440793 |
| DOIs | |
| Publication status | Published - 11 Apr 2024 |
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