FDA's and EMA's approval of brentuximab vedotin for advanced Hodgkin lymphoma: Another player in the town? (CROSBI ID 282274)
Prilog u časopisu | pregledni rad (znanstveni) | međunarodna recenzija
Podaci o odgovornosti
Milunović, Vibor ; Mišura Jakobac, Karla ; Kursar, Marin ; Mandac Rogulj, Inga ; Ostojić Kolonić, Slobodanka
engleski
FDA's and EMA's approval of brentuximab vedotin for advanced Hodgkin lymphoma: Another player in the town?
ECHELON-1 study is a randomized open-labeled controlled trial investigating whether addition of brentuximab vedotin to chemotherapy offers benefit over the standard chemotherapy regimen in advanced Hodgkin lymphoma. After a median follow-up of 24.6 months, it has met its primary endpoint the reduction of modified progression-free survival being 23 percent. However, the beneficial effects have not been seen across all subgroups leading to further questions. The main aim of this review is to tackle these questions to provide the reader with in-depth insight of pros and cons of this novel, promising but ultimately controversial regimen.
Hodgkin lymphoma ; brentuximab vedotin ; induction chemotherapy ; monoclonal antibodies.
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Podaci o izdanju
103 (3)
2019.
145-151
objavljeno
0902-4441
1600-0609
10.1111/ejh.13269
Povezanost rada
Kliničke medicinske znanosti