Efficacy and Safety of Isatuximab, Carfilzomib, and Dexamethasone (IsaKd) in Multiple Myeloma Patients at the First Relapse After Autologous Stem Cell Transplantation and Lenalidomide Maintenance: Results from the Multicenter, Real-Life AENEID Study

<b>Background</b>: In the randomized, phase-3 IKEMA trial, the triplet isatuximab, carfilzomib, and dexamethasone (IsaKd) demonstrated superior clinical benefit compared to those of carfilzomib and dexamethasone alone in patients with relapsed/refractory multiple myeloma after 1-3 prior treatments. <b>Methods</b>: Our real-world, AENEID study aimed to evaluate the efficacy and safety of IsaKd in patients who relapsed after frontline lenalidomide treatment, poorly represented in the IKEMA trial. Specifically, in the present multicenter analysis, we enrolled eighty-two patients who received, between April 2022 and September 2024 and outside of clinical trials, at least one cycle of IsaKd as a second-line treatment at the first relapse after induction therapy, autologous stem cell transplantation (ASCT), and lenalidomide maintenance. <b>Results</b>: After a median follow-up time of 12.9 months (range, 1-77), the overall response rate, at least a very good partial response rate, and median progression-free survival time were 79.3%, 56.1%, and 24.4 months, respectively. This slightly lower performance compared to that in the IKEMA study may be attributed to the well-known poor prognostic impact of lenalidomide refractoriness (len-R), developed by all our patients during maintenance therapy, and to a higher proportion of patients with extramedullary disease present in our series, which was identified as the only factor significantly affecting the PFS in multivariable analysis. The median overall survival was not reached, as in the pivotal trial, while the 1-year survival probability was 85.1%. Regarding the safety profile, our findings were consistent with those of the IKEMA trial, with no new safety signals reported. <b>Conclusions</b>: These real-world data support the use of IsaKd as a valuable option for len-R MM patients relapsing after the first-line therapy, including ASCT and lenalidomide maintenance.

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Publication Details

Journal
Pharmaceuticals
Published
2025-04-19
DOI
https://doi.org/10.3390/ph18040595
Citations
2
Primary Topic
Multiple Myeloma Research and Treatments
Type
article
Field-Weighted Citation Impact
3.54

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article

Efficacy and Safety of Isatuximab, Carfilzomib, and Dexamethasone (IsaKd) in Multiple Myeloma Patients at the First Relapse After Autologous Stem Cell Transplantation and Lenalidomide Maintenance: Results from the Multicenter, Real-Life AENEID Study

Emanuela Resta, Concetta Conticello, Enrica Antonia Martino, Daniela Roccotelli et al.
2 citations
Pharmaceuticals
Multiple Myeloma Research and Treatments
3.54
article

Efficacy and Safety of Isatuximab, Carfilzomib, and Dexamethasone (IsaKd) in Multiple Myeloma Patients at the First Relapse After Autologous Stem Cell Transplantation and Lenalidomide Maintenance: Results from the Multicenter, Real-Life AENEID Study

Emanuela Resta, Concetta Conticello, Enrica Antonia Martino, Daniela Roccotelli, Candida Germano, Olga Battisti, Pellegrino Musto, Giuseppe Mele, Maria Teresa Petrucci, Roberta Della Pepa, Fabrizio Pane, Salvatore Palmieri, Anna Mele, Paola Curci, Francesca Fazio, Daniele Derudas, Domenico Pastore, Nicola Sgherza, Giuseppe Tarantini, Francesco Di Raimondo, Bernardo Rossini, Giulia Palazzo, Simona Rasola
article en
2 citations

Abstract

<b>Background</b>: In the randomized, phase-3 IKEMA trial, the triplet isatuximab, carfilzomib, and dexamethasone (IsaKd) demonstrated superior clinical benefit compared to those of carfilzomib and dexamethasone alone in patients with relapsed/refractory multiple myeloma after 1-3 prior treatments. <b>Methods</b>: Our real-world, AENEID study aimed to evaluate the efficacy and safety of IsaKd in patients who relapsed after frontline lenalidomide treatment, poorly represented in the IKEMA trial. Specifically, in the present multicenter analysis, we enrolled eighty-two patients who received, between April 2022 and September 2024 and outside of clinical trials, at least one cycle of IsaKd as a second-line treatment at the first relapse after induction therapy, autologous stem cell transplantation (ASCT), and lenalidomide maintenance. <b>Results</b>: After a median follow-up time of 12.9 months (range, 1-77), the overall response rate, at least a very good partial response rate, and median progression-free survival time were 79.3%, 56.1%, and 24.4 months, respectively. This slightly lower performance compared to that in the IKEMA study may be attributed to the well-known poor prognostic impact of lenalidomide refractoriness (len-R), developed by all our patients during maintenance therapy, and to a higher proportion of patients with extramedullary disease present in our series, which was identified as the only factor significantly affecting the PFS in multivariable analysis. The median overall survival was not reached, as in the pivotal trial, while the 1-year survival probability was 85.1%. Regarding the safety profile, our findings were consistent with those of the IKEMA trial, with no new safety signals reported. <b>Conclusions</b>: These real-world data support the use of IsaKd as a valuable option for len-R MM patients relapsing after the first-line therapy, including ASCT and lenalidomide maintenance.

PharmaceuticalsVol. 18(4)
Casa Sollievo della Sofferenza (IT), University of Catania (IT), Ospedale Antonio Cardarelli (IT), Ospedale A. Perrino (IT), Azienda Ospedaliera S.Giuseppe Moscati (IT), Federico II University Hospital (IT), Policlinico Universitario di Catania (IT), Istituto Tumori Bari (IT), Ospedale Annunziata di Cosenza (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT), University of Calabria (IT), University of Bari Aldo Moro (IT), Sapienza University of Rome (IT)
Università degli Studi di Palermo, Università degli Studi di Messina
Openalex Percentile: Top 8%
Multiple Myeloma Research and Treatments
3.54
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