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A phase 1b dose-escalation study of carfilzomib in combination with thalidomide and dexamethasone in patients with relapsed/refractory systemic immunoglobulin light chain amyloidosis.

Authors :
Ravichandran S
Hall A
Jenner M
Garg M
Kishore B
Lachmann H
Gillmore J
Pitchford A
Oughton JB
Mahmood S
Sachchithantham S
Hawkins P
Brown S
Wechalekar A
Source :
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis [Amyloid] 2023 Sep; Vol. 30 (3), pp. 290-296. Date of Electronic Publication: 2023 May 22.
Publication Year :
2023

Abstract

Introduction: Proteasome inhibitors are the backbone of AL amyloidosis treatment - bortezomib being most widely used. Carfilzomib is a proteasome inhibitor licenced to treat multiple myeloma; autonomic and peripheral neuropathy are uncommon toxicities with carfilzomib. There is limited data on the use of carfilzomib in AL amyloidosis. Here, we report the results of a phase Ib dose-escalation study of Carfilzomib-Thalidomide-Dexamethasone (KTD) in relapsed/refractory AL amyloidosis.<br />Results: The trial registered 11 patients from 6 UK centres from September 2017 to January 2019; 10 patients received at least one dose of trial treatment. 80 adverse events were reported from 10 patients in the 1 <superscript>st</superscript> three cycles. One patient experienced dose-limiting toxicity (acute kidney injury) at a dose of 45 mg/m <superscript>2,</superscript> and another patient had a SAR (fever). Five patients experienced an AE ≥ grade 3. There were no haematologic, infectious, or cardiac AE ≥ grade 3. The overall haematological response rate (ORR) at the end of three cycles of treatment was 60%.<br />Conclusion: Carfilzomib 45 mg/m <superscript>2</superscript> weekly can be safely given with thalidomide and dexamethasone. The efficacy and tolerability profile appears comparable to other agents in relapsed AL amyloidosis. These data provide a framework for further studies of carfilzomib combinations in AL amyloidosis.

Details

Language :
English
ISSN :
1744-2818
Volume :
30
Issue :
3
Database :
MEDLINE
Journal :
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Publication Type :
Academic Journal
Accession number :
37216268
Full Text :
https://doi.org/10.1080/13506129.2023.2169124