2025
De-escalated Teclistamab dosing in relapsed/refractory multiple myeloma: Czech myeloma group real-world evidence analysis
ŠTORK, Martin; Jakub RADOCHA; Jana MIHALYOVA; Ivan SPICKA; Tomas PIKA et al.Základní údaje
Originální název
De-escalated Teclistamab dosing in relapsed/refractory multiple myeloma: Czech myeloma group real-world evidence analysis
Autoři
ŠTORK, Martin; Jakub RADOCHA; Jana MIHALYOVA; Ivan SPICKA; Tomas PIKA; Alexandra JUNGOVA; Ivanna BOICHUK; Klára MENŠÍKOVÁ; Jan STRAUB; Frantisek SEDLAK; Jiri MINARIK; Petra KRHOVSKA; Denisa NOVAKOVA; Michaela HORNAKOVA; Zdeňka KNECHTOVÁ; Nela SENDLEROVÁ; Tereza DEKOJOVA; Vladimir MAISNAR; Tomas JELINEK; Roman HAJEK a Luděk POUR
Vydání
Annals of hematology, New York, Springer Verlag, 2025, 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: 2.400 v roce 2024
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/25:00143747
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Multiple myeloma; Teclistamab; Immunotherapy; Real-world-evidence
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 24. 2. 2026 10:22, Mgr. Tereza Miškechová
Anotace
V originále
Teclistamab, a BCMAxCD3 bispecific antibody, demonstrates high efficacy in relapsed/refractory multiple myeloma (RRMM). However, optimal dosing strategies outside clinical trials remain undefined. Thus, we performed a retrospective, multicentre analysis of 73 RRMM patients treated with teclistamab monotherapy at Czech Myeloma Group centres between 2023 and 2025. The study compared efficacy and safety between patients receiving standard weekly dosing and those with reduced-frequency dosing. The whole cohort had a median age of 67 years; 68.5% were penta-refractory. Dosing was de-escalated in 24.7% of patients, typically within one month of treatment initiation. Median progression-free survival (PFS) was 9.41 months and was comparable between weekly and non-weekly groups (9.1 vs. 11.3 months; p = 0.141), despite a significantly lower relative dose intensity in the latter (60.5% vs. 87.0%; p < 0.001). Infection rates and severe adverse events were similar between groups. A lower incidence of neutropenia was observed with less frequent dosing, but this did not translate into reduced infection burden. In conclusion, in real-world practice, early de-escalation of teclistamab dosing appears to maintain clinical efficacy. These findings support ongoing efforts to individualize treatment schedules with the aim of balancing effectiveness, tolerability, and patient-specific factors in BCMA-targeted therapy.