Cyclophosphamide, Bortezomib and Methylprednisolone (CyBorMe) for the Treatment of AL Amyloidosis: Initial Experience From a Single Center.

AL amyloidosis CyBorD CyBorMe Organ response

Journal

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
ISSN: 0971-4502
Titre abrégé: Indian J Hematol Blood Transfus
Pays: India
ID NLM: 9425818

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 10 09 2020
accepted: 02 02 2021
entrez: 8 11 2021
pubmed: 9 11 2021
medline: 9 11 2021
Statut: ppublish

Résumé

The use of cyclophosphamide, bortezomib and dexamethasone (CyBorD) is widely accepted in the treatment of AL amyloidosis (AL). Recently, the substitution of dexamethasone by methylprednisolone (CyBorMe) appeared to improve response rates and survival outcomes. All consecutive newly diagnosed AL amyloidosis treated with CyBorMe from 01/19 to 08/20 were evaluated. A historic cohort of patients treated with CyBorD was used for comparison (01/13-08/20). Methylprednisolone was given IV at 500 mg weekly for 4 weeks in the CyBorMe group. 43 patients were treated with CyBorD and 14 with CyBorMe. After a median of 4 cycles of CyBorD and 3 cycles of CyBorMe, Hematological Response was seen in 90.6% and 92.8% of cases, including CR in 28.5% and 35.7%, VGPR in 33.3% and 35.7% and PR in 30.9% and 21.4% for CyBorD and CyBorMe, respectively. Time to first response was faster in the CyBorMe group (4 vs. 6 weeks) and cardiac response was observed in 44% and 31% of patients treated with CyBorMe and CyBorD, respectively. CyBorMe appeared to be efficacious and well tolerated in patients with AL amyloidosis. Prospective studies with CyBorMe in the stage III/IV group are warranted aiming to minimize toxicity.

Identifiants

pubmed: 34744351
doi: 10.1007/s12288-021-01406-z
pii: 1406
pmc: PMC8523610
doi:

Types de publication

Journal Article

Langues

eng

Pagination

675-678

Informations de copyright

© Indian Society of Hematology and Blood Transfusion 2021.

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Auteurs

Victor H Jimenez-Zepeda (VH)

Tom Baker Cancer Center/University of Calgary, 1331 29th St, NW, Calgary, AB T2N 4N2 Canada.

Holly Lee (H)

Tom Baker Cancer Center/University of Calgary, 1331 29th St, NW, Calgary, AB T2N 4N2 Canada.

Nowell Fine (N)

Division of Cardiology, Department of Cardiac Sciences, Libin Cardiovascular Institute of Alberta, Calgary, AB Canada.

Sylvia McCulloch (S)

Tom Baker Cancer Center/University of Calgary, 1331 29th St, NW, Calgary, AB T2N 4N2 Canada.

Jason Tay (J)

Tom Baker Cancer Center/University of Calgary, 1331 29th St, NW, Calgary, AB T2N 4N2 Canada.

Peter Duggan (P)

Tom Baker Cancer Center/University of Calgary, 1331 29th St, NW, Calgary, AB T2N 4N2 Canada.

Paola Neri (P)

Tom Baker Cancer Center/University of Calgary, 1331 29th St, NW, Calgary, AB T2N 4N2 Canada.

Nizar Bahlis (N)

Tom Baker Cancer Center/University of Calgary, 1331 29th St, NW, Calgary, AB T2N 4N2 Canada.

Classifications MeSH