2023
Daratumumab with lenalidomide and dexamethasone in relapsed or refractory multiple myeloma patients – real world evidence analysis
ŠTORK, Martin; Ivan SPICKA; Jakub RADOCHA; Jiri MINARIK; Tomas JELINEK et al.Základní údaje
Originální název
Daratumumab with lenalidomide and dexamethasone in relapsed or refractory multiple myeloma patients – real world evidence analysis
Autoři
ŠTORK, Martin; Ivan SPICKA; Jakub RADOCHA; Jiri MINARIK; Tomas JELINEK; Alexandra JUNGOVA; Petr PAVLICEK; Lenka POSPISILOVA; Frantisek SEDLAK; Jan STRAUB; Tomas PIKA; Zdeňka KNECHTOVÁ; Anna FIDRICHOVA; Ivanna BOICHUK; Sabina ŠEVČÍKOVÁ; Vladimir MAISNAR; Roman HAJEK a Luděk POUR
Vydání
Annals of Hematology, NEW YORK, SPRINGER, 2023, 0939-5555
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30205 Hematology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.000
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/23:00130652
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Multiple myeloma; Treatment; Response rate; Relapse
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 30. 1. 2024 08:08, Mgr. Tereza Miškechová
Anotace
V originále
We performed real world evidence (RWE) analysis of daratumumab, lenalidomide and dexamethasone (Dara-Rd) versus lenalidomide and dexamethasone (Rd) treatment in relapsed/refractory multiple myeloma patients (RRMM). In total, 240 RRMM patients were treated with Dara-Rd from 2016 to 2022 outside of clinical trials in all major Czech hematology centers. As a reference, 531 RRMM patients treated with Rd were evaluated. Patients’ data were recorded in the Czech Registry of Monoclonal Gammopathies (RMG). Partial response (PR) or better response (ORR) was achieved in significantly more patients in Dara-Rd than in Rd group (91.2% vs. 69.9%; p < 0.001). The median progression free survival (PFS) was 26.9 months in the Dara-Rd and 12.8 months in the Rd group (p < 0.001). Median overall survival (OS) was not reached in the Dara-Rd compared to 27.2 months in the Rd group (p = 0.023). In patients with 1–3 previous treatment lines, there was significant PFS benefit of Dara-Rd compared to Rd (median PFS not reached vs. 13.2 months; p < 0.001). In patients with > 3 previous treatment lines, there was no significant PFS benefit of Dara-Rd treatment (7.8 months vs. 9.9 months; p = 0.874), similarly in patients refractory to PI + IMIDs (11.5 months vs. 9.2 months; p = 0.376). In RWE conditions, the median PFS in RRMM patients treated with Dara-Rd is shorter when compared to clinical trials. In heavily pretreated RRMM patients, efficacy of Dara-Rd treatment is limited; best possible outcomes of Dara-Rd are achieved in minimally pretreated patients.
Návaznosti
| LX22NPO5102, projekt VaV |
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| NU21-03-00076, projekt VaV |
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