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Venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory AL amyloidosis

Authors :
Vikram J. Premkumar
Suzanne Lentzsch
Samuel Pan
Divaya Bhutani
Joshua Richter
Sundar Jagannath
Michaela Liedtke
Arnaud Jaccard
Ashutosh D. Wechalekar
Raymond Comenzo
Vaishali Sanchorawala
Bruno Royer
Michael Rosenzweig
Jason Valent
Stefan Schönland
Rafael Fonseca
Sandy Wong
Prashant Kapoor
Source :
Blood Cancer Journal, Vol 11, Iss 1, Pp 1-10 (2021)
Publication Year :
2021
Publisher :
Nature Publishing Group, 2021.

Abstract

Abstract Venetoclax is efficacious in relapsed/refractory t(11;14) multiple myeloma, thus warranting investigation in light-chain amyloidosis (AL). This retrospective cohort includes 43 patients with previously treated AL, from 14 centers in the US and Europe. Thirty-one patients harbored t(11;14), 11 did not, and one t(11;14) status was unknown. Patients received a venetoclax-containing regimen for at least one 21- or 28-day cycle; the median prior treatments was three. The hematologic response rate for all patients was 68%; 63% achieved VGPR/CR. t(11;14) patients had higher hematologic response (81% vs. 40%) and higher VGPR/CR rate (78% vs. 30%, odds ratio: 0.12, 95% CI 0.02–0.62) than non-t(11;14) patients. For the unsegregated cohort, median progression-free survival (PFS) was 31.0 months and median OS was not reached (NR). For t(11;14), median PFS was NR and for non-t(11;14) median PFS was 6.7 months (HR: 0.14, 95% CI 0.04–0.53). Multivariate analysis incorporating age, sex, prior lines of therapy, and disease stage suggested a risk reduction for progression or death in t(11;14) patients. Median OS was NR for either subgroup. The organ response rate was 38%; most responders harbored t(11;14). Grade 3 or higher adverse events occurred in 19% with 7% due to infections. These promising results require confirmation in a randomized clinical trial.

Details

Language :
English
ISSN :
20445385
Volume :
11
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Blood Cancer Journal
Publication Type :
Academic Journal
Accession number :
edsdoj.013c38376a484b75ab2ff3152ca40fbf
Document Type :
article
Full Text :
https://doi.org/10.1038/s41408-020-00397-w