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


ABSTRACT:

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.

Funding

Janssen Pharmaceuticals, Takeda Pharmaceutical Company Limited.

SUBMITTER: Groen K 

PROVIDER: S-EPMC10481174 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature

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

Groen Kaz K   Stege Claudia A M CAM   Nasserinejad Kazem K   de Heer Koen K   van Kampen Roel J W RJW   Leys Rineke B L RBL   Thielen Noortje N   Westerman Matthijs M   Wu Ka-Lung KL   Ludwig Inge I   Issa Djamila E DE   Velders Gerjo A GA   Vekemans Marie-Christiane MC   Timmers Gert-Jan GJ   de Boer Fransien F   Tick Lidwine W LW   Verbrugge Annelies A   Buitenhuis Danny D   Cunha Sonia M SM   van der Spek Ellen E   de Waal Esther G M EGM   Sohne Maaike M   Sonneveld Pieter P   Nijhof Inger S IS   Klein Saskia K SK   van de Donk Niels W C J NWCJ   Levin Mark-David MD   Ypma Paula F PF   Zweegman Sonja S  

EClinicalMedicine 20230829


<h4>Background</h4>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.<h4>Methods</h4>In this phase II multicenter HOVON-143 study, IMWG Frailty index based intermediate-fit patients, were treated with 9 induction cycles of Ixa-Dara-de  ...[more]

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