Efficacy of ixazomib, lenalidomide, dexamethasone regimen in daratumumab-exposed relapsed/refractory multiple myeloma patients: A retrospective analysis
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
Grant support
LX22NPO5102
Ministry of Education, Youth, and Sports of the Czech Republic
LX22NPO5107
Ministry of Education, Youth, and Sports of the Czech Republic
FNBr
The Ministry of Health, Czech Republic-Conceptual Development of Research Organization
65269705
The Ministry of Health, Czech Republic-Conceptual Development of Research Organization
NU21-03-00076
Ministry of Health of the Czech Republic
PubMed
39187373
DOI
10.1111/ejh.14292
Knihovny.cz E-resources
- Keywords
- daratumumab, ixazomib, relapsed/refractory multiple myeloma,
- MeSH
- Drug Resistance, Neoplasm * MeSH
- Dexamethasone * administration & dosage therapeutic use MeSH
- Adult MeSH
- Glycine * analogs & derivatives administration & dosage therapeutic use MeSH
- Lenalidomide * administration & dosage therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Multiple Myeloma * drug therapy mortality MeSH
- Antibodies, Monoclonal * therapeutic use administration & dosage MeSH
- Retreatment MeSH
- Antineoplastic Combined Chemotherapy Protocols * therapeutic use adverse effects MeSH
- Recurrence MeSH
- Retrospective Studies MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Boron Compounds * administration & dosage therapeutic use MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- daratumumab MeSH Browser
- Dexamethasone * MeSH
- Glycine * MeSH
- ixazomib MeSH Browser
- Lenalidomide * MeSH
- Antibodies, Monoclonal * MeSH
- Boron Compounds * MeSH
We performed retrospective analysis of relapsed/refractory multiple myeloma (RRMM) patients previously exposed to daratumumab treated with ixazomib, lenalidomide, dexamethasone (IRd) regimen in real clinical practice. Our aim was to evaluate efficacy of IRd in these patients and select a subset of patients that would benefit from this treatment the most. In total, we analyzed 43 daratumumab-exposed RRMM patients treated in our center. Minimal response or better was achieved by 53.5% of patients from the cohort. Median progression free survival (PFS) was 4.56 months (95% CI: 2.56, 8.03) and median overall survival (OS) was 28.92 months (95% CI: 5.4, NR). Duration of response (DOR) was evaluable in 28 patients and reached a median of 21.3 months (95% CI: 6.85, NR). Next, we evaluated hazard ratios (HR) for OS and PFS. There was improved OS in patients that were not-triple refractory or worse (HR = 0.39, 95%Cl (0.14; 1.10), p = .07) and in patients, that had less than three previous lines of treatment (LOT) (HR = 0.13, 95%Cl (0.03; 0.6) p = .003). Similar to OS, there was improved PFS in patients, that were not triple-refractory or worse (HR = 0.52, 95%Cl (0.25; 1.10), p = .08). We concluded, that the best survival benefit for RRMM patients pretreated with daratumumab to IRd regimen was observed in patients that were not triple-refractory and had less than three previous lines of treatment (LOT). The DOR in these patients was 21.3 months (95% CI: 6.85, NR).
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