Cargando…

Depth of response and response kinetics of isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma

The IKEMA study (Randomized, Open Label, Multicenter Study Assessing the Clinical Benefit of Isatuximab Combined With Carfilzomib [Kyprolis®] and Dexamethasone Versus Carfilzomib With Dexamethasone in Patients With Relapse and/or Refractory Multiple Myeloma Previously Treated With 1 to 3 Prior Lines...

Descripción completa

Detalles Bibliográficos
Autores principales: Martin, Thomas, Mikhael, Joseph, Hajek, Roman, Kim, Kihyun, Suzuki, Kenshi, Hulin, Cyrille, Garg, Mamta, Quach, Hang, Sia, Hanlon, George, Anup, Konstantinova, Tatiana, Risse, Marie-Laure, Asset, Gaelle, Macé, Sandrine, van de Velde, Helgi, Moreau, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Hematology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636327/
https://www.ncbi.nlm.nih.gov/pubmed/35594559
http://dx.doi.org/10.1182/bloodadvances.2021006713
_version_ 1784824921564643328
author Martin, Thomas
Mikhael, Joseph
Hajek, Roman
Kim, Kihyun
Suzuki, Kenshi
Hulin, Cyrille
Garg, Mamta
Quach, Hang
Sia, Hanlon
George, Anup
Konstantinova, Tatiana
Risse, Marie-Laure
Asset, Gaelle
Macé, Sandrine
van de Velde, Helgi
Moreau, Philippe
author_facet Martin, Thomas
Mikhael, Joseph
Hajek, Roman
Kim, Kihyun
Suzuki, Kenshi
Hulin, Cyrille
Garg, Mamta
Quach, Hang
Sia, Hanlon
George, Anup
Konstantinova, Tatiana
Risse, Marie-Laure
Asset, Gaelle
Macé, Sandrine
van de Velde, Helgi
Moreau, Philippe
author_sort Martin, Thomas
collection PubMed
description The IKEMA study (Randomized, Open Label, Multicenter Study Assessing the Clinical Benefit of Isatuximab Combined With Carfilzomib [Kyprolis®] and Dexamethasone Versus Carfilzomib With Dexamethasone in Patients With Relapse and/or Refractory Multiple Myeloma Previously Treated With 1 to 3 Prior Lines; #NCT03275285) was a randomized, open-label, multicenter phase 3 study investigating isatuximab plus carfilzomib and dexamethasone (Isa-Kd) vs Kd in patients with relapsed multiple myeloma. This subanalysis analyzed the depth of response of Isa-Kd vs Kd. The primary end point was progression-free survival (PFS); secondary end points included overall response rate, very good partial response or better (≥VGPR) rate, complete response (CR) rate, and minimal residual disease (MRD) negativity rate (assessed in patients with ≥VGPR by next-generation sequencing at a 10(−5) sensitivity level). At a median follow-up of 20.7 months, deeper responses were observed in the Isa-Kd arm vs the Kd arm, with ≥VGPR 72.6% vs 56.1% and CR of 39.7% vs 27.6%, respectively. MRD negativity occurred in 53 (29.6%) of 179 patients in the Isa-Kd arm vs 16 (13.0%) of 123 patients in the Kd arm, with 20.1% (Isa-Kd, 36 of 179 patients) vs 10.6% (Kd, 13 of 123 patients) reaching MRD-negative CR status. Achieving MRD negativity resulted in better PFS in both arms. A positive PFS treatment effect was seen with Isa-Kd in both MRD-negative patients (hazard ratio, 0.578; 95% CI, 0.052-6.405) and MRD-positive patients (hazard ratio, 0.670; 95% CI, 0.452-0.993). Exploratory analysis indicates that both current CR and MRD-negative CR rates are underestimated due to M-protein interference (potential adjusted CR rate, 45.8%; potential adjusted MRD-negative CR rate, 24.0%). In conclusion, there was a clinically meaningful improvement in depth of response with Isa-Kd. The CR rate in Isa-Kd was 39.7%. Mass spectrometry suggests that the potential adjusted CR rate could reach an unprecedented 45.8% of patients treated with Isa-Kd.
format Online
Article
Text
id pubmed-9636327
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher The American Society of Hematology
record_format MEDLINE/PubMed
spelling pubmed-96363272022-11-07 Depth of response and response kinetics of isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma Martin, Thomas Mikhael, Joseph Hajek, Roman Kim, Kihyun Suzuki, Kenshi Hulin, Cyrille Garg, Mamta Quach, Hang Sia, Hanlon George, Anup Konstantinova, Tatiana Risse, Marie-Laure Asset, Gaelle Macé, Sandrine van de Velde, Helgi Moreau, Philippe Blood Adv Clinical Trials and Observations The IKEMA study (Randomized, Open Label, Multicenter Study Assessing the Clinical Benefit of Isatuximab Combined With Carfilzomib [Kyprolis®] and Dexamethasone Versus Carfilzomib With Dexamethasone in Patients With Relapse and/or Refractory Multiple Myeloma Previously Treated With 1 to 3 Prior Lines; #NCT03275285) was a randomized, open-label, multicenter phase 3 study investigating isatuximab plus carfilzomib and dexamethasone (Isa-Kd) vs Kd in patients with relapsed multiple myeloma. This subanalysis analyzed the depth of response of Isa-Kd vs Kd. The primary end point was progression-free survival (PFS); secondary end points included overall response rate, very good partial response or better (≥VGPR) rate, complete response (CR) rate, and minimal residual disease (MRD) negativity rate (assessed in patients with ≥VGPR by next-generation sequencing at a 10(−5) sensitivity level). At a median follow-up of 20.7 months, deeper responses were observed in the Isa-Kd arm vs the Kd arm, with ≥VGPR 72.6% vs 56.1% and CR of 39.7% vs 27.6%, respectively. MRD negativity occurred in 53 (29.6%) of 179 patients in the Isa-Kd arm vs 16 (13.0%) of 123 patients in the Kd arm, with 20.1% (Isa-Kd, 36 of 179 patients) vs 10.6% (Kd, 13 of 123 patients) reaching MRD-negative CR status. Achieving MRD negativity resulted in better PFS in both arms. A positive PFS treatment effect was seen with Isa-Kd in both MRD-negative patients (hazard ratio, 0.578; 95% CI, 0.052-6.405) and MRD-positive patients (hazard ratio, 0.670; 95% CI, 0.452-0.993). Exploratory analysis indicates that both current CR and MRD-negative CR rates are underestimated due to M-protein interference (potential adjusted CR rate, 45.8%; potential adjusted MRD-negative CR rate, 24.0%). In conclusion, there was a clinically meaningful improvement in depth of response with Isa-Kd. The CR rate in Isa-Kd was 39.7%. Mass spectrometry suggests that the potential adjusted CR rate could reach an unprecedented 45.8% of patients treated with Isa-Kd. The American Society of Hematology 2022-05-23 /pmc/articles/PMC9636327/ /pubmed/35594559 http://dx.doi.org/10.1182/bloodadvances.2021006713 Text en Copyright © 2022 The American Society of Hematology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Clinical Trials and Observations
Martin, Thomas
Mikhael, Joseph
Hajek, Roman
Kim, Kihyun
Suzuki, Kenshi
Hulin, Cyrille
Garg, Mamta
Quach, Hang
Sia, Hanlon
George, Anup
Konstantinova, Tatiana
Risse, Marie-Laure
Asset, Gaelle
Macé, Sandrine
van de Velde, Helgi
Moreau, Philippe
Depth of response and response kinetics of isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma
title Depth of response and response kinetics of isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma
title_full Depth of response and response kinetics of isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma
title_fullStr Depth of response and response kinetics of isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma
title_full_unstemmed Depth of response and response kinetics of isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma
title_short Depth of response and response kinetics of isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma
title_sort depth of response and response kinetics of isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma
topic Clinical Trials and Observations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636327/
https://www.ncbi.nlm.nih.gov/pubmed/35594559
http://dx.doi.org/10.1182/bloodadvances.2021006713
work_keys_str_mv AT martinthomas depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT mikhaeljoseph depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT hajekroman depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT kimkihyun depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT suzukikenshi depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT hulincyrille depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT gargmamta depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT quachhang depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT siahanlon depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT georgeanup depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT konstantinovatatiana depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT rissemarielaure depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT assetgaelle depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT macesandrine depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT vandeveldehelgi depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma
AT moreauphilippe depthofresponseandresponsekineticsofisatuximabpluscarfilzomibanddexamethasoneinrelapsedmultiplemyeloma