State-of-the-art review on AL amyloidosis in Western Countries: Epidemiology, health economics, risk assessment and therapeutic management of a rare disease

Amyloidosis is the term to define a broad array of rare protein misfolding syndromes. Among them, light chain (AL) amyloidosis is the most common, affecting roughly 10 people per million/year. The core purpose of the present literature review is to shed light on the academic and clinical knowledge o...

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Vydáno v:	Blood reviews Ročník 59; s. 101040
Hlavní autoři:	Sabinot, Alice, Ghetti, Gianni, Pradelli, Lorenzo, Bellucci, Stefania, Lausi, Antonella, Palladini, Giovanni
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	England Elsevier Ltd 01.05.2023
Témata:	AL amyloidosis Amyloidosis - diagnosis Amyloidosis - epidemiology Amyloidosis - etiology Epidemiology Humans Immunoglobulin Light-chain Amyloidosis - diagnosis Immunoglobulin Light-chain Amyloidosis - epidemiology Immunoglobulin Light-chain Amyloidosis - therapy Light-chain amyloidosis PRISMA guidelines Quality of Life Rare Diseases Risk Assessment Risk-staging Systematic literature review cTnI PR PS BNP LDex CyBorDM dLFC Epidemiology HD-Dex UK cTnT Risk-staging PFS US PRISMA guidelines BorD AL amyloidosis Bor MS AL IT ER ES MDex EU SF36-v1 AT SF36-v2 NCI DaraLDex ASCT IMiD NL Systematic literature review SES N/A RS NR CyBorD FR L N QoL HDM SF36 BU NT-proBNP T NRes MPredDex VGPR DaraBorDex CA GE SR eGFR GI OS SW CI GR m MPred PMP TBor y Light-chain amyloidosis HD HR-QoL
ISSN:	0268-960X, 1532-1681, 1532-1681
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