FDA Approval Summary: Brentuximab Vedotin in First-Line Treatment of Peripheral T-Cell Lymphoma.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
05 2019
Historique:
received: 01 02 2019
accepted: 01 03 2019
pubmed: 28 3 2019
medline: 12 5 2020
entrez: 28 3 2019
Statut: ppublish

Résumé

In November 2018, the U.S. Food and Drug Administration (FDA) approved brentuximab vedotin (BV) for the treatment of adult patients with previously untreated systemic anaplastic large cell lymphoma or other CD30-expressing peripheral T-cell lymphomas (PTCL), including angioimmunoblastic T-cell lymphoma and PTCL not otherwise specified, in combination with cyclophosphamide, doxorubicin, and prednisone (CHP). Approval was based on ECHELON-2, a randomized, double-blind, actively controlled trial that compared BV+CHP with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) in 452 patients with newly diagnosed, CD30-expressing PTCL. Efficacy was based on independent review facility-assessed progression-free survival (PFS). The median PFS was 48.2 months with BV+CHP versus 20.8 months with CHOP, resulting in a hazard ratio (HR) of 0.71 (95% confidence interval [CI]: 0.54-0.93). The trial also demonstrated improvement in overall survival (HR 0.66; 95% CI: 0.46-0.95), complete response rate (68% vs. 56%), and overall response rate (83% vs. 72%) with BV+CHP. The most common adverse reactions (incidence ≥20%) observed ≥2% more with BV+CHP were nausea, diarrhea, fatigue or asthenia, mucositis, pyrexia, vomiting, and anemia. Peripheral neuropathy rates were similar (52% with BV+CHP, 55% with CHOP). Through the Real-Time Oncology Review pilot program, which allows FDA early access to key data, FDA granted this approval less than 2 weeks after official submission of the application. IMPLICATIONS FOR PRACTICE: This is the first U.S. Food and Drug Administration approval for treatment of patients with newly diagnosed peripheral T-cell lymphomas (PTCL). Improvement in progression-free and overall survival over cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy, which has been the standard of care for decades, is unprecedented. The new regimen represents a major advance for the frontline treatment of patients with CD30-expressing PTCL.

Identifiants

pubmed: 30914464
pii: theoncologist.2019-0098
doi: 10.1634/theoncologist.2019-0098
pmc: PMC6516120
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Brentuximab Vedotin 7XL5ISS668

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e180-e187

Informations de copyright

Published 2019. This article is a U.S. Government work and is in the public domain in the USA.

Déclaration de conflit d'intérêts

Disclosures of potential conflicts of interest may be found at the end of this article.

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Auteurs

Nicholas C Richardson (NC)

Office of Hematology and Oncology Products, Center for Drug Evaluation and Research, Silver Spring, Maryland, USA nicholas.richardson@fda.hhs.gov.

Yvette L Kasamon (YL)

Office of Hematology and Oncology Products, Center for Drug Evaluation and Research, Silver Spring, Maryland, USA.

Haiyan Chen (H)

Office of Biostatistics, Center for Drug Evaluation and Research, Silver Spring, Maryland, USA.

R Angelo de Claro (RA)

Office of Hematology and Oncology Products, Center for Drug Evaluation and Research, Silver Spring, Maryland, USA.

Jingjing Ye (J)

Office of Biostatistics, Center for Drug Evaluation and Research, Silver Spring, Maryland, USA.

Gideon M Blumenthal (GM)

Office of Hematology and Oncology Products, Center for Drug Evaluation and Research, Silver Spring, Maryland, USA.
Oncology Center of Excellence, U.S. Food and Drug Administration, Silver Spring, Maryland, USA.

Ann T Farrell (AT)

Office of Hematology and Oncology Products, Center for Drug Evaluation and Research, Silver Spring, Maryland, USA.

Richard Pazdur (R)

Office of Hematology and Oncology Products, Center for Drug Evaluation and Research, Silver Spring, Maryland, USA.
Oncology Center of Excellence, U.S. Food and Drug Administration, Silver Spring, Maryland, USA.

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