| Literature DB >> 34783272 |
Vaishali Sanchorawala1, Mario Boccadoro2, Morie Gertz3, Ute Hegenbart4, Efstathios Kastritis5, Heather Landau6, Peter Mollee7, Ashutosh Wechalekar8, Giovanni Palladini9.
Abstract
AL amyloidosis is a systemic amyloidosis and is associated with an underlying plasma cell dyscrasia. High dose intravenous melphalan and autologous stem cell transplantation was developed for the treatment of AL amyloidosis in the early 1990s and was prompted by its success in multiple myeloma. This application has evolved significantly over the past three decades. These guidelines provide a comprehensive assessment of eligibility criteria, stem cell collection and mobilisation strategies and regimens, risk-adapted melphalan dosing, role for induction and consolidation therapies, specific supportive care management, long-term outcome with respect to survival, haematologic response and relapse and organ responses following stem cell transplantation. These guidelines are developed by the experts in the field on behalf of the stem cell transplant working group of the International Society of Amyloidosis (ISA) and European Haematology Association (EHA).Entities:
Keywords: AL amyloidosis; melphalan; patient selection; stem cell transplantation; supportive care
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Year: 2021 PMID: 34783272 DOI: 10.1080/13506129.2021.2002841
Source DB: PubMed Journal: Amyloid ISSN: 1350-6129 Impact factor: 7.141