articleNew England Journal of MedicineNov 3, 2010BRONZE OA

Brentuximab Vedotin (SGN-35) for Relapsed CD30-Positive Lymphomas

The University of Texas MD Anderson Cancer Center · Washington University in St. Louis · +3 more institutions

PubMed
Indexed incrossrefpubmed

Abstract

Background

Hodgkin's lymphoma and anaplastic large-cell lymphoma are the two most common tumors expressing CD30. Previous attempts to target the CD30 antigen with monoclonal-based therapies have shown minimal activity. To enhance the antitumor activity of CD30-directed therapy, the antitubulin agent monomethyl auristatin E (MMAE) was attached to a CD30-specific monoclonal antibody by an enzyme-cleavable linker, producing the antibody-drug conjugate brentuximab vedotin (SGN-35).

Methods

In this phase 1, open-label, multicenter dose-escalation study, we administered brentuximab vedotin (at a dose of 0.1 to 3.6 mg per kilogram of body weight) every 3 weeks to 45 patients with relapsed or refractory CD30-positive hematologic cancers, primarily Hodgkin's lymphoma and anaplastic large-cell lymphoma. Patients had received a median of three previous chemotherapy regimens (range, one to seven), and 73% had undergone autologous stem-cell transplantation.

Citation impact

1,347
total citations
FWCI
67.59
Percentile
100%
References
36
Citations per year

Authors

7

Topics & keywords

Keywords
  • Brentuximab vedotin
  • CD30
  • Medicine
  • Antibody-drug conjugate
  • Monoclonal antibody
  • Lymphoma
  • Anaplastic large-cell lymphoma
  • Conjugate
UN Sustainable Development Goals
  • Good health and well-being
No related works found for this paper.