Report of Consensus Panel 6 from the 11 th International Workshop on Waldenström's Macroglobulinemia on Management of Waldenström's Macroglobulinemia Related Amyloidosis.
AL amyloidosis
Diagnostic criteria
Response assessment
Therapy
Waldenström macroglobulinemia
Journal
Seminars in hematology
ISSN: 1532-8686
Titre abrégé: Semin Hematol
Pays: United States
ID NLM: 0404514
Informations de publication
Date de publication:
Mar 2023
Mar 2023
Historique:
received:
08
03
2023
accepted:
09
03
2023
medline:
19
6
2023
pubmed:
26
4
2023
entrez:
26
4
2023
Statut:
ppublish
Résumé
Consensus Panel 6 (CP6) of the 11th International Workshop on Waldenström's Macroglobulinemia (IWWM-11) was tasked with reviewing the state of the art for diagnosis, prognosis, and therapy of AL amyloidosis associated with Waldenström macroglobulinemia (WM). Since significant advances have been made in the management of AL amyloidosis an update for this rare disease associated with WM was necessary. The key recommendations from IWWM-11 CP6 included: (1) The need to improve the diagnostic process by recognizing red flags and using biomarkers and imaging; (2) The essential tests for appropriate workup; (3) The diagnostic flowchart, including mandatory amyloid typing, that improves the differential diagnosis with transthyretin amyloidosis; (4) Criteria for therapy response assessment; (5) State of the art of the treatment including therapy of wild type transthyretin amyloidosis associated with WM.
Identifiants
pubmed: 37099030
pii: S0037-1963(23)00022-7
doi: 10.1053/j.seminhematol.2023.03.002
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
113-117Informations de copyright
Copyright © 2023 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest GM has no disclosures. MCM received research funding from Beigene, and consulting fees from BMS, GSK, Jansen Cilag, and CDR life. SRS received research funding and/or consulting fees from Beigene, Cellectar Biosciences, and ADC Therapeutics. GB declares participation on advisory boards and speakers bureau for Janssen-Cilag, Bristol Myers Squibb and Novartis. SPT received research funding, and/or consulting fees from Abbvie/Pharmacyclics Inc., Janssen Oncology Inc., Beigene Inc., Eli Lilly Pharmaceuticals, and Bristol Myers Squibb. CFL reports: consultancy: Janssen, BeiGene, BMS, Amgen, GSK; reserach grants: Janssen, Amgen, BMS; Advisory: BeiGene, Janssen, Amgen, BMS, GSK. JSM declares participation on advisory boards and consulting services, on behalf of my Institution, for Abbvie, Amgen, BMS, Celgene, GSK, Haemalogix, Janssen-Cilag, Karyopharm, MSD, Novartis, Pfizer, Takeda, Regeneron, Roche, Sanofi, and SecuraBio. MD received honoraria from Amgen, Bristol Myers Squibb, GSK, Janssen, Beigene Inc, Sanofi and Takeda. RGS declares honoraria from Amgen, Takeda, Janssen, Incyte, Astellas, BeiGene, AstraZeneca, Pfizer; and research funding from Novartis, Gilead, Astellas, Janssen; and participation in advisory boards for Amgen, Pharmacyclics, Takeda. XC reports no disclosures. MG reports no disclosures.