Guidelines for non-transplant chemotherapy for treatment of systemic AL amyloidosis: EHA-ISA working group.


Journal

Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
ISSN: 1744-2818
Titre abrégé: Amyloid
Pays: England
ID NLM: 9433802

Informations de publication

Date de publication:
Mar 2023
Historique:
pubmed: 16 7 2022
medline: 7 3 2023
entrez: 15 7 2022
Statut: ppublish

Résumé

This guideline has been developed jointly by the European Society of Haematology and International Society of Amyloidosis recommending non-transplant chemotherapy treatment for patients with AL amyloidosis. A review of literature and grading of evidence as well as expert recommendations by the ESH and ISA guideline committees. The recommendations of this committee suggest that treatment follows the clinical presentation which determines treatment tolerance tempered by potential side effects to select and modify use of drugs in AL amyloidosis. All patients with AL amyloidosis should be considered for clinical trials where available. Daratumumab-VCD is recommended from most untreated patients (VCD or VMDex if daratumumab is unavailable). At relapse, the two guiding principles are the depth and duration of initial response, use of a class of agents not previously exposed as well as the limitation imposed by patients' fitness/frailty and end organ damage. Targeted agents like venetoclax need urgent prospective evaluation. Future prospective trials should include advanced stage patients to allow for evidence-based treatment decisions. Therapies targeting amyloid fibrils or those reducing the proteotoxicity of amyloidogenic light chains/oligomers are urgently needed.

Sections du résumé

BACKGROUND UNASSIGNED
This guideline has been developed jointly by the European Society of Haematology and International Society of Amyloidosis recommending non-transplant chemotherapy treatment for patients with AL amyloidosis.
METHODS UNASSIGNED
A review of literature and grading of evidence as well as expert recommendations by the ESH and ISA guideline committees.
RESULTS AND CONCLUSIONS UNASSIGNED
The recommendations of this committee suggest that treatment follows the clinical presentation which determines treatment tolerance tempered by potential side effects to select and modify use of drugs in AL amyloidosis. All patients with AL amyloidosis should be considered for clinical trials where available. Daratumumab-VCD is recommended from most untreated patients (VCD or VMDex if daratumumab is unavailable). At relapse, the two guiding principles are the depth and duration of initial response, use of a class of agents not previously exposed as well as the limitation imposed by patients' fitness/frailty and end organ damage. Targeted agents like venetoclax need urgent prospective evaluation. Future prospective trials should include advanced stage patients to allow for evidence-based treatment decisions. Therapies targeting amyloid fibrils or those reducing the proteotoxicity of amyloidogenic light chains/oligomers are urgently needed.

Identifiants

pubmed: 35838162
doi: 10.1080/13506129.2022.2093635
doi:

Substances chimiques

Amyloid 0

Types de publication

Guideline Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

3-17

Auteurs

Ashutosh D Wechalekar (AD)

National Amyloidosis Centre, University College London (Royal Free Campus), London, UK.

M Teresa Cibeira (MT)

Amyloidosis and Myeloma Unit, Hospital Clinic of Barcelona, IDIBAPS, Barcelona, Spain.

Simon D Gibbs (SD)

Victorian and Tasmanian Amyloidosis Service, Eastern Health Monash University Clinical School, Box Hill, VIC, Australia.

Arnaud Jaccard (A)

Hematology Department, French Reference Center for AL Amyloidosis (Limoges-Poitiers), CHU Limoges, Limoges, France.

Shaji Kumar (S)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Giampaolo Merlini (G)

Amyloidosis Research and Treatment Center, Foundation "Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo" and Department of Molecular Medicine, University of Pavia, Pavia, Italy.

Giovanni Palladini (G)

Amyloidosis Research and Treatment Center, Foundation "Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo" and Department of Molecular Medicine, University of Pavia, Pavia, Italy.

Vaishali Sanchorawala (V)

Amyloidosis Center, Boston University School of Medicine and Boston Medical Center, Boston, MA, USA.

Stefan Schönland (S)

Medical Department V, Amyloidosis Center, University Hospital Heidelberg, Heidelberg, Germany.

Christopher Venner (C)

BC Cancer, Vancouver Centre, Vancouver, Canada.

Mario Boccadoro (M)

Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.

Efstathios Kastritis (E)

Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.

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