Systemic light chain amyloidosis, version 2.2023, NCCN Clinical Practice Guidelines in Oncology Guidelines


Authors: Kumar, S. K.; Callander, N. S.; Adekola, K.; Anderson, L. D. Jr; Baljevic, M.; Campagnaro, E.; Castillo, J. J.; Costello, C.; D'Angelo, C.; Devarakonda, S.; Elsedawy, N.; Garfall, A.; Godby, K.; Hillengass, J.; Holmberg, L.; Htut, M.; Huff, C. A.; Hultcrantz, M.; Kang, Y.; Larson, S.; Lee, H. C.; Liedtke, M.; Martin, T.; Omel, J.; Rosenberg, A.; Sborov, D.; Valent, J.; Berardi, R.; Kumar, R.
Title: Systemic light chain amyloidosis, version 2.2023, NCCN Clinical Practice Guidelines in Oncology
Abstract: Primary systemic light chain amyloidosis (SLCA) is characterized by production of light chains that get converted to amyloid fibrils with an affinity for visceral organs and causing organ dysfunction. The therapy for SLCA is directed to recovering the function of the affected organs by targeting the abnormal plasma cell clone and slowing deposition of amyloid fibrils. The NCCN Guidelines for SLCA provide recommendations for workup, diagnosis, and treatment of primary as well as previously treated SLCA.
Journal Title: Journal of the National Comprehensive Cancer Network
Volume: 21
Issue: 1
ISSN: 1540-1405
Publisher: Harborside Press  
Date Published: 2023-01-01
Start Page: 67
End Page: 81
Language: English
DOI: 10.6004/jnccn.2023.0001
PUBMED: 36652935
PROVIDER: scopus
DOI/URL:
Notes: Article -- DOI is currently broken -- Export Date: 1 February 2023 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
Related MSK Work