Blood Res 2017; 52(4):
Published online December 31, 2017
https://doi.org/10.5045/br.2017.52.4.243
© The Korean Society of Hematology
1Division of Hematology-Oncology, Department of Medicine, Chung-Ang University Hospital, Seoul, Korea.
2Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Correspondence to : Won Seog Kim, M.D., Ph.D. Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul 06351, Korea. wskimsmc@skku.edu
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Brentuximab vedotin (BV), a potent antibody-drug conjugate, targets the CD30 antigen. Owing to the remarkable efficacy shown in CD30-positive lymphomas, such as Hodgkin's lymphoma and systemic anaplastic large-cell lymphoma, BV was granted accelerated approval in 2011 by the US Food and Drug Administration. Thereafter, many large-scale trials in various situations have been performed, which led to extensions of the original indication. The aim of this review was to describe the latest updates on clinical trials of BV and the in-practice guidance for the use of BV.
Keywords Brentuximab vedotin, CD30, Antibody-drug conjugate, Hodgkin's lymphoma, Anaplastic large cell lymphoma
Blood Res 2017; 52(4): 243-253
Published online December 31, 2017 https://doi.org/10.5045/br.2017.52.4.243
Copyright © The Korean Society of Hematology.
Jun Ho Yi1, Seok Jin Kim2, and Won Seog Kim2*
1Division of Hematology-Oncology, Department of Medicine, Chung-Ang University Hospital, Seoul, Korea.
2Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Correspondence to:Won Seog Kim, M.D., Ph.D. Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul 06351, Korea. wskimsmc@skku.edu
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Brentuximab vedotin (BV), a potent antibody-drug conjugate, targets the CD30 antigen. Owing to the remarkable efficacy shown in CD30-positive lymphomas, such as Hodgkin's lymphoma and systemic anaplastic large-cell lymphoma, BV was granted accelerated approval in 2011 by the US Food and Drug Administration. Thereafter, many large-scale trials in various situations have been performed, which led to extensions of the original indication. The aim of this review was to describe the latest updates on clinical trials of BV and the in-practice guidance for the use of BV.
Keywords: Brentuximab vedotin, CD30, Antibody-drug conjugate, Hodgkin's lymphoma, Anaplastic large cell lymphoma
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Abbreviations: CR, complete response; ORR, overall response rate; PFS, progression-free survival; SCT, stem cell transplantation (either autologous and/or allogeneic)..
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