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

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 no...

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Autores principales: Premkumar, Vikram J., Lentzsch, Suzanne, Pan, Samuel, Bhutani, Divaya, Richter, Joshua, Jagannath, Sundar, Liedtke, Michaela, Jaccard, Arnaud, Wechalekar, Ashutosh D., Comenzo, Raymond, Sanchorawala, Vaishali, Royer, Bruno, Rosenzweig, Michael, Valent, Jason, Schönland, Stefan, Fonseca, Rafael, Wong, Sandy, Kapoor, Prashant
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801694/
https://www.ncbi.nlm.nih.gov/pubmed/33431806
http://dx.doi.org/10.1038/s41408-020-00397-w
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author Premkumar, Vikram J.
Lentzsch, Suzanne
Pan, Samuel
Bhutani, Divaya
Richter, Joshua
Jagannath, Sundar
Liedtke, Michaela
Jaccard, Arnaud
Wechalekar, Ashutosh D.
Comenzo, Raymond
Sanchorawala, Vaishali
Royer, Bruno
Rosenzweig, Michael
Valent, Jason
Schönland, Stefan
Fonseca, Rafael
Wong, Sandy
Kapoor, Prashant
author_facet Premkumar, Vikram J.
Lentzsch, Suzanne
Pan, Samuel
Bhutani, Divaya
Richter, Joshua
Jagannath, Sundar
Liedtke, Michaela
Jaccard, Arnaud
Wechalekar, Ashutosh D.
Comenzo, Raymond
Sanchorawala, Vaishali
Royer, Bruno
Rosenzweig, Michael
Valent, Jason
Schönland, Stefan
Fonseca, Rafael
Wong, Sandy
Kapoor, Prashant
author_sort Premkumar, Vikram J.
collection PubMed
description 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.
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spelling pubmed-78016942021-01-21 Venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory AL amyloidosis Premkumar, Vikram J. Lentzsch, Suzanne Pan, Samuel Bhutani, Divaya Richter, Joshua Jagannath, Sundar Liedtke, Michaela Jaccard, Arnaud Wechalekar, Ashutosh D. Comenzo, Raymond Sanchorawala, Vaishali Royer, Bruno Rosenzweig, Michael Valent, Jason Schönland, Stefan Fonseca, Rafael Wong, Sandy Kapoor, Prashant Blood Cancer J Article 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. Nature Publishing Group UK 2021-01-11 /pmc/articles/PMC7801694/ /pubmed/33431806 http://dx.doi.org/10.1038/s41408-020-00397-w Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Premkumar, Vikram J.
Lentzsch, Suzanne
Pan, Samuel
Bhutani, Divaya
Richter, Joshua
Jagannath, Sundar
Liedtke, Michaela
Jaccard, Arnaud
Wechalekar, Ashutosh D.
Comenzo, Raymond
Sanchorawala, Vaishali
Royer, Bruno
Rosenzweig, Michael
Valent, Jason
Schönland, Stefan
Fonseca, Rafael
Wong, Sandy
Kapoor, Prashant
Venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory AL amyloidosis
title Venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory AL amyloidosis
title_full Venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory AL amyloidosis
title_fullStr Venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory AL amyloidosis
title_full_unstemmed Venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory AL amyloidosis
title_short Venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory AL amyloidosis
title_sort venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory al amyloidosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801694/
https://www.ncbi.nlm.nih.gov/pubmed/33431806
http://dx.doi.org/10.1038/s41408-020-00397-w
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