MINARIK, J., T. PIKA, J. RADOCHA, A. JUNGOVA, J. STRAUB, T. JELINEK, Luděk POUR, P. PAVLICEK, M. MISTRIK, Lucie BROŽOVÁ, P. KRHOVSKA, K. MACHALKOVA, P. JINDRA, I. SPICKA, H. PLONKOVA, Martin ŠTORK, J. BACOVSKY, L. CAPKOVA, M. SYKORA, P. KESSLER, L. STEJSKAL, A. HEINDORFER, J. ULLRYCHOVA, T. SKACEL, V. MAISNAR and R. HAJEK. Survival benefit of ixazomib, lenalidomide and dexamethasone (IRD) over lenalidomide and dexamethasone (Rd) in relapsed and refractory multiple myeloma patients in routine clinical practice. BMC Cancer. LONDON: BMC, 2021, vol. 21, No 1, p. 1-13. ISSN 1471-2407. Available from: https://dx.doi.org/10.1186/s12885-020-07732-1.
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Basic information
Original name Survival benefit of ixazomib, lenalidomide and dexamethasone (IRD) over lenalidomide and dexamethasone (Rd) in relapsed and refractory multiple myeloma patients in routine clinical practice
Authors MINARIK, J. (203 Czech Republic, guarantor), T. PIKA (203 Czech Republic), J. RADOCHA (203 Czech Republic), A. JUNGOVA (203 Czech Republic), J. STRAUB (203 Czech Republic), T. JELINEK (203 Czech Republic), Luděk POUR (203 Czech Republic, belonging to the institution), P. PAVLICEK (203 Czech Republic), M. MISTRIK (203 Czech Republic), Lucie BROŽOVÁ (203 Czech Republic), P. KRHOVSKA (203 Czech Republic), K. MACHALKOVA (203 Czech Republic), P. JINDRA (203 Czech Republic), I. SPICKA (203 Czech Republic), H. PLONKOVA (203 Czech Republic), Martin ŠTORK (203 Czech Republic, belonging to the institution), J. BACOVSKY (203 Czech Republic), L. CAPKOVA (203 Czech Republic), M. SYKORA (203 Czech Republic), P. KESSLER (203 Czech Republic), L. STEJSKAL (203 Czech Republic), A. HEINDORFER (203 Czech Republic), J. ULLRYCHOVA (203 Czech Republic), T. SKACEL (203 Czech Republic), V. MAISNAR (203 Czech Republic) and R. HAJEK (203 Czech Republic).
Edition BMC Cancer, LONDON, BMC, 2021, 1471-2407.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30204 Oncology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.638
RIV identification code RIV/00216224:14110/21:00120101
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1186/s12885-020-07732-1
UT WoS 000610557500001
Keywords in English Multiple myeloma; Ixazomib; Lenalidomide; Dexamethasone; Clinical trial; Patient registry
Tags 14110212, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 3/6/2021 09:42.
Abstract
Background We have performed a head to head comparison of all-oral triplet combination of ixazomib, lenalidomide and dexamethasone (IRD) versus lenalidomide and dexamethasone (RD) in patients with relapsed and refractory multiple myeloma (RRMM) in the routine clinical practice. Methods A total of 344 patients treated with IRD (N = 127) or RD (N = 217) were selected for analysis from the Czech Registry of Monoclonal Gammopathies (RMG). Descriptive statistics were used to assess patient's characteristics associated with the respective therapy. The primary endpoint was progression free survival (PFS), secondary end points included response rates and overall survival (OS). Survival endpoints were plotted using Kaplan-Meier methodology at 95% Greenwood confidence interval. Univariable and multivariable Cox proportional hazards models were used to evaluate the effect of treatment regimens and the significance of uneven variables. Statistical tests were performed at significance level 0.05. Results In the whole cohort, median PFS for IRD was 17.5 and for RD was 11.5 months favoring the all-oral triplet, p = 0.005; in patients within relapse 1-3, the median PFS was 23.1 vs 11.6 months, p = 0.001. The hazard ratio for PFS was 0.67 (95% confidence interval [CI] 0.51-0.89, p = 0.006). The PFS advantage translated into improved OS for patients treated with IRD, median 36.6 months vs 26.0 months (p = 0.008). The overall response rate (ORR) was 73.0% in the IRD group vs 66.2% in the RD group with a complete response rate (CR) of 11.1% vs 8.8%, and very good partial response (VGPR) 22.2% vs 13.9%, IRD vs RD respectively. The IRD regimen was most beneficial in patients <= 75 years with ISS I, II, and in the first and second relapse. Patients with the presence of extramedullary disease did not benefit from IRD treatment (median PFS 6.5 months). Both regimens were well tolerated, and the incidence of total as well as grade 3/4 toxicities was comparable. Conclusions Our analysis confirms the results of the TOURMALINE-MM1 study and shows benefit of all-oral triplet IRD treatment versus RD doublet. It demonstrates that the addition of ixazomib to RD improves key survival endpoints in patients with RRMM in a routine clinical setting.
Links
NV17-29343A, research and development projectName: Analýza mikroprostředí kostní dřeně u extramedulárního relapsu mnohočetného myelomu
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