Systemic AL Amyloidosis: Current Approaches to Diagnosis and Management

Abstract. AL amyloidosis is characterized by a low-level expansion of an indolent, small plasma cell clone that produces amyloidogenic light chains. Amyloid aggregates or preceding intermediaries cause direct cell damage through their proteotoxicity, and amyloid deposits distort tissue architecture,...

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Main Authors: Despina Fotiou, Meletios Athanasios Dimopoulos, Efstathios Kastritis
Format: Article
Language:English
Published: Wolters Kluwer 2020-08-01
Series:HemaSphere
Online Access:http://journals.lww.com/10.1097/HS9.0000000000000454
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spelling doaj-c55f210cd98148ae942b265b80ed260d2020-11-25T01:25:10ZengWolters KluwerHemaSphere2572-92412020-08-0144e45410.1097/HS9.0000000000000454202008000-00012Systemic AL Amyloidosis: Current Approaches to Diagnosis and ManagementDespina Fotiou0Meletios Athanasios Dimopoulos1Efstathios Kastritis2Plasma Cell Dyscrasia Unit, Department of Clinical Therapeutics, National and Kapodistrian University of Athens, Athens, Greece.Plasma Cell Dyscrasia Unit, Department of Clinical Therapeutics, National and Kapodistrian University of Athens, Athens, Greece.Plasma Cell Dyscrasia Unit, Department of Clinical Therapeutics, National and Kapodistrian University of Athens, Athens, Greece.Abstract. AL amyloidosis is characterized by a low-level expansion of an indolent, small plasma cell clone that produces amyloidogenic light chains. Amyloid aggregates or preceding intermediaries cause direct cell damage through their proteotoxicity, and amyloid deposits distort tissue architecture, and, eventually, lead to organ impairment. It is a rare, underdiagnosed disease with a diverse clinical presentation depending on the organ tropism of the amyloid fibrils; cardiac and renal involvement is most common, but any organ can be affected, excluding the central nervous system. A high level of awareness and a systematic approach using newly emerging screening biomarkers is required to achieve early diagnosis. Management should be multidisciplinary as supportive management tailored to management of organ dysfunction is paramount to survival and minimization of treatment-associated toxicity. The initial therapeutic aim is to rapidly eliminate the clonal plasma cell that produces the circulating amyloid precursor and achieve a complete hematologic response, and if possible with undetectable minimal residual disease as assessed by next-generation methods (flow and sequencing), with minimal toxicity. Treatment is tailored to the initial risk assessment of the patients. Treatments are based on regimens adapted from the expanding options that are available for multiple myeloma patients and hematological response rates have improved. Organ response rates are strongly associated with deeper hematologic response but usually lag behind hematological response and are also dependent on the initial organ function reserve. Agents directed against the amyloid deposits have been explored to aid amyloid clearance and improve organ function, but data are still negative.http://journals.lww.com/10.1097/HS9.0000000000000454
collection DOAJ
language English
format Article
sources DOAJ
author Despina Fotiou
Meletios Athanasios Dimopoulos
Efstathios Kastritis
spellingShingle Despina Fotiou
Meletios Athanasios Dimopoulos
Efstathios Kastritis
Systemic AL Amyloidosis: Current Approaches to Diagnosis and Management
HemaSphere
author_facet Despina Fotiou
Meletios Athanasios Dimopoulos
Efstathios Kastritis
author_sort Despina Fotiou
title Systemic AL Amyloidosis: Current Approaches to Diagnosis and Management
title_short Systemic AL Amyloidosis: Current Approaches to Diagnosis and Management
title_full Systemic AL Amyloidosis: Current Approaches to Diagnosis and Management
title_fullStr Systemic AL Amyloidosis: Current Approaches to Diagnosis and Management
title_full_unstemmed Systemic AL Amyloidosis: Current Approaches to Diagnosis and Management
title_sort systemic al amyloidosis: current approaches to diagnosis and management
publisher Wolters Kluwer
series HemaSphere
issn 2572-9241
publishDate 2020-08-01
description Abstract. AL amyloidosis is characterized by a low-level expansion of an indolent, small plasma cell clone that produces amyloidogenic light chains. Amyloid aggregates or preceding intermediaries cause direct cell damage through their proteotoxicity, and amyloid deposits distort tissue architecture, and, eventually, lead to organ impairment. It is a rare, underdiagnosed disease with a diverse clinical presentation depending on the organ tropism of the amyloid fibrils; cardiac and renal involvement is most common, but any organ can be affected, excluding the central nervous system. A high level of awareness and a systematic approach using newly emerging screening biomarkers is required to achieve early diagnosis. Management should be multidisciplinary as supportive management tailored to management of organ dysfunction is paramount to survival and minimization of treatment-associated toxicity. The initial therapeutic aim is to rapidly eliminate the clonal plasma cell that produces the circulating amyloid precursor and achieve a complete hematologic response, and if possible with undetectable minimal residual disease as assessed by next-generation methods (flow and sequencing), with minimal toxicity. Treatment is tailored to the initial risk assessment of the patients. Treatments are based on regimens adapted from the expanding options that are available for multiple myeloma patients and hematological response rates have improved. Organ response rates are strongly associated with deeper hematologic response but usually lag behind hematological response and are also dependent on the initial organ function reserve. Agents directed against the amyloid deposits have been explored to aid amyloid clearance and improve organ function, but data are still negative.
url http://journals.lww.com/10.1097/HS9.0000000000000454
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