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First report of ibrutinib in IgM-related amyloidosis: few responses, poor tolerability, and short survival

TO THE EDITOR: Light-chain amyloidosis (AL) is a rare systemic protein deposition disorder that belongs to the group of plasma cell dyscrasias. Approximately 10% to 22% of cases are associated with symptomatic multiple myeloma or Waldenström macroglobulinemia (WM). The disease is characterized by

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Bibliographische Detailangaben
Hauptverfasser: Pica, Tomas (VerfasserIn) , Hegenbart, Ute (VerfasserIn) , Maier, Bettina (VerfasserIn) , Kimmich, Christoph (VerfasserIn) , Schönland, Stefan (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2018
In: Blood
Year: 2018, Jahrgang: 131, Heft: 3, Pages: 368-371
ISSN:1528-0020
DOI:10.1182/blood-2017-09-806463
Online-Zugang:Verlag, Volltext: http://dx.doi.org/10.1182/blood-2017-09-806463
Verlag, Volltext: http://www.bloodjournal.org/content/131/3/368
Volltext
Verfasserangaben:Tomas Pika, Ute Hegenbart, Pavla Flodrova, Bettina Maier, Christoph Kimmich, Stefan O. Schönland
Beschreibung
Zusammenfassung:TO THE EDITOR: Light-chain amyloidosis (AL) is a rare systemic protein deposition disorder that belongs to the group of plasma cell dyscrasias. Approximately 10% to 22% of cases are associated with symptomatic multiple myeloma or Waldenström macroglobulinemia (WM). The disease is characterized by
Beschreibung:First edition: November 27, 2017
Gesehen am 02.10.2018
Beschreibung:Online Resource
ISSN:1528-0020
DOI:10.1182/blood-2017-09-806463

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