Ixazomib, daratumumab and low-dose dexamethasone in intermediate-fit patients with newly diagnosed multiple myeloma: an open-label phase 2 trial

被引:6
|
作者
Groen, Kaz [1 ,2 ]
Stege, Claudia A. M. [1 ,2 ]
Nasserinejad, Kazem [3 ,4 ]
de Heer, Koen [5 ]
van Kampen, Roel J. W. [6 ]
Leys, Rineke B. L. [7 ]
Thielen, Noortje [8 ]
Westerman, Matthijs [9 ]
Wu, Ka-Lung [10 ]
Ludwig, Inge [11 ]
Issa, Djamila E. [12 ]
Velders, Gerjo A. [13 ]
Vekemans, Marie-Christiane [14 ]
Timmers, Gert-Jan [15 ]
de Boer, Fransien [16 ]
Tick, Lidwine W. [17 ]
Verbrugge, Annelies [3 ]
Buitenhuis, Danny [3 ]
Cunha, Sonia M. [3 ]
van der Spek, Ellen [18 ]
de Waal, Esther G. M. [19 ]
Sohne, Maaike [20 ]
Sonneveld, Pieter [21 ]
Nijhof, Inger S. [20 ]
Klein, Saskia K. [22 ,23 ]
van der Donk, Niels W. C. J. [1 ,2 ]
Levin, Mark-David [24 ]
Ypma, Paula F. [25 ]
Zweegman, Sonja [1 ,2 ,26 ]
机构
[1] Vrije Univ Amsterdam, Dept Hematol, Amsterdam UMC, Amsterdam, Netherlands
[2] Canc Ctr Amsterdam, Treatment & Qual Life, Amsterdam, Netherlands
[3] Erasmus MC Canc Inst, HOVON Data Ctr, Dept Hematol, Rotterdam, Netherlands
[4] Cytel Inc, Therapeut Dev Team, Innovat Stat Consulting, Waltham, MA USA
[5] Flevoziekenhuis, Dept Internal Med, Almere, Netherlands
[6] Zuyderland Hosp, Dept Internal Med, Sittard Geleen, Netherlands
[7] Maasstad Hosp, Dept Internal Med, Rotterdam, Netherlands
[8] Diakonessen Hosp, Dept Internal Med, Utrecht, Netherlands
[9] Northwest Clin, Dept Internal Med, Alkmaar, Netherlands
[10] ZNA Stuivenberg, Dept Hematol, Antwerp, Belgium
[11] Ziekenhuis Bernhoven, Dept Internal Med, Uden, Netherlands
[12] Jeroen Bosch Hosp, Dept Internal Med, Den Bosch, Netherlands
[13] Gelderse Vallei, Dept Internal Med, Ede, Netherlands
[14] UCL, Dept Hematol, Clin Univ St Luc, Brussels, Belgium
[15] Amstelland Hosp, Dept Internal Med, Amstelveen, Netherlands
[16] Ikazia Hosp, Dept Internal Med, Rotterdam, Netherlands
[17] Maxima Med Ctr, Dept Internal Med, Eindhoven, Netherlands
[18] Rijnstate Hosp, Dept Internal Med, Arnhem, Netherlands
[19] Med Ctr Leeuwarden, Dept Internal Med, Leeuwarden, Netherlands
[20] Antonius Ziekenhuis, Dept Internal Med, Nieuwegein, Netherlands
[21] Erasmus MC Canc Inst, Dept Hematol, Rotterdam, Netherlands
[22] Meander Med Ctr, Dept Internal Med, Amersfoort, Netherlands
[23] Univ Med Ctr Groningen, Dept Hematol, Groningen, Netherlands
[24] Albert Schweitzer Hosp, Dept Internal Med, Dordrecht, Netherlands
[25] Haga Hosp, Dept Internal Med, The Hague, Netherlands
[26] Dept Hematol, Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
关键词
Multiple myeloma; Elderly; Daratumumab; Ixazomib; Intermediate-fit; IMWG frailty index; STEM-CELL TRANSPLANTATION; ORAL IXAZOMIB; LENALIDOMIDE; MAINTENANCE; BORTEZOMIB; SURVIVAL; THALIDOMIDE; PREDNISONE; MELPHALAN; CONSENSUS;
D O I
10.1016/j.eclinm.2023.102167
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The outcome of non-transplant eligible newly diagnosed multiple myeloma (NDMM) patients is heterogeneous, partly depending on frailty level. The aim of this study was to prospectively investigate the efficacy and safety of Ixazomib-Daratumumab-low-dose dexamethasone (Ixa-Dara-dex) in NDMM intermediate-fit patients. Methods In this phase II multicenter HOVON-143 study, IMWG Frailty index based intermediate-fit patients, were treated with 9 induction cycles of Ixa-Dara-dex, followed by maintenance with ID for a maximum of 2 years. The primary endpoint was overall response rate on induction treatment. Patients were included from October 2017 until May 2019. Trial Registration Number: NTR6297. Findings Sixty-five patients were included. Induction therapy resulted in an overall response rate of 71%. Early mortality was 1.5%. At a median follow-up of 41.0 months, median progression-free survival (PFS) was 18.2 months and 3-year overall survival 83%. Discontinuation of therapy occurred in 77% of patients, 49% due to progression, 9% due to toxicity, 8% due to incompliance, 3% due to sudden death and 8% due to other reasons. Dose modifications of ixazomib were required frequently (37% and 53% of patients during induction and maintenance, respectively), mainly due to, often low grade, polyneuropathy. During maintenance 23% of patients received daratumumab alone. Global quality of life (QoL) improved significantly and was clinically relevant, which persisted during maintenance treatment. Interpretation Ixazomib-Daratumumab-low-dose dexamethasone as first line treatment in intermediate -fit NDMM patients is safe and improves global QoL. However, efficacy was limited, partly explained by ixazomib-induced toxicity, hampering long term tolerability of this 3-drug regimen. This highlights the need for more efficacious and tolerable regimens improving the outcome in vulnerable intermediate -fit patients.
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