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FDA's and EMA's approval of brentuximab vedotin for advanced Hodgkin lymphoma: Another player in the town?
- Source :
-
European journal of haematology [Eur J Haematol] 2019 Sep; Vol. 103 (3), pp. 145-151. Date of Electronic Publication: 2019 Jun 17. - Publication Year :
- 2019
-
Abstract
- 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.<br /> (© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
- Subjects :
- Antineoplastic Agents, Immunological administration & dosage
Antineoplastic Agents, Immunological adverse effects
Antineoplastic Combined Chemotherapy Protocols adverse effects
Brentuximab Vedotin administration & dosage
Brentuximab Vedotin adverse effects
Clinical Trials, Phase III as Topic
Drug Approval
Europe
Hodgkin Disease diagnosis
Hodgkin Disease etiology
Humans
Multicenter Studies as Topic
Neoplasm Metastasis
Neoplasm Staging
Randomized Controlled Trials as Topic
Treatment Outcome
United States
United States Food and Drug Administration
Antineoplastic Agents, Immunological therapeutic use
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Brentuximab Vedotin therapeutic use
Hodgkin Disease drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1600-0609
- Volume :
- 103
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- European journal of haematology
- Publication Type :
- Academic Journal
- Accession number :
- 31166030
- Full Text :
- https://doi.org/10.1111/ejh.13269