2019
Treatment of Relapsed/Refractory Hodgkin Lymphoma: Real-World Data from the Czech Republic and Slovakia
KRÁL, Zdeněk, Jozef MICHALKA, Heidi MOCIKOVA, Jana MARKOVA, Alice SYKOROVA et. al.Základní údaje
Originální název
Treatment of Relapsed/Refractory Hodgkin Lymphoma: Real-World Data from the Czech Republic and Slovakia
Autoři
KRÁL, Zdeněk (203 Česká republika, garant, domácí), Jozef MICHALKA (703 Slovensko, domácí), Heidi MOCIKOVA (203 Česká republika), Jana MARKOVA (203 Česká republika), Alice SYKOROVA (203 Česká republika), David BELADA (203 Česká republika), Alexandra JUNGOVA (203 Česká republika), Samuel VOKURKA (203 Česká republika), Marie LUKASOVA (203 Česká republika), Vit PROCHAZKA (203 Česká republika), Juraj DURAS (203 Česká republika), Roman HAJEK (203 Česká republika), Ladislav DUŠEK (203 Česká republika, domácí), L'ubos DRGONA (703 Slovensko), Miriam LADICKA (703 Slovensko), Veronika BALLOVA (756 Švýcarsko) a Andrei VRANOVSKY (703 Slovensko)
Vydání
Journal of Cancer, Australia, IVYSPRING INT PUBL, 2019, 1837-9664
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30204 Oncology
Stát vydavatele
Austrálie
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.565
Kód RIV
RIV/00216224:14110/19:00111949
Organizační jednotka
Lékařská fakulta
UT WoS
000484111400004
Klíčová slova anglicky
antibody-drug conjugate; CD30; brentuximab vedotin; Hodgkin lymphoma; registries; stem cell transplantation
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 11. 5. 2020 10:38, Mgr. Tereza Miškechová
Anotace
V originále
Introduction: Clinical trials have demonstrated the effectiveness of the CD30-targeted antibody- drug conjugate brentuximab vedotin (BV) for the treatment of relapsed/refractory Hodgkin lymphoma (R/R HL). In this study, we report on outcomes with BV in a real-world setting using data collected in clinics in the Czech Republic and Slovakia. Patients and Methods: Clinical and epidemiological data for patients with R/R HL who received treatment with BV at eight centers across the Czech Republic and Slovakia were examined. Data were amalgamated and analyzed retrospectively. Results: Clinical data for 58 patients (median age: 30.5 years) with R/R HL who received BV during the course of their treatment were collected and analyzed. Patients had received a median of 3 prior treatment regimens and most (91%) were treated with BV after relapse following autologous stem cell transplantation. Therapeutic responses after BV included 19 (33%) complete responses (CRs) and 8 (14%) partial responses. CRs occurred more frequently in patients who had received fewer prior treatment regimens. The 1-, 2-, and 3-year overall survival (OS) rates from initiation of BV were 78%, 62%, and 41%, respectively. Conclusion: Response rates and OS in this analysis of BV in real-world settings in the Czech Republic and Slovakia were consistent with those reported for pivotal clinical trials and from previous studies outside the clinical trial setting. The results support the efficacy of BV for treatment of R/R HL in real-life clinical practice.