Six events that shaped antibody approvals in oncology
A little over twenty-five years ago, the European Medicines Agency (EMA) and the Food and Drug Administration (FDA) approved the chimeric antibody rituximab which fundamentally altered the landscape of anti-cancer drugs. While only a few antibodies were approved in the immediate years that followed...
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Frontiers Media S.A.
2025-02-01
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Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2025.1533796/full |
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author | Suman Paul Suman Paul Shibin Zhou Shibin Zhou |
author_facet | Suman Paul Suman Paul Shibin Zhou Shibin Zhou |
author_sort | Suman Paul |
collection | DOAJ |
description | A little over twenty-five years ago, the European Medicines Agency (EMA) and the Food and Drug Administration (FDA) approved the chimeric antibody rituximab which fundamentally altered the landscape of anti-cancer drugs. While only a few antibodies were approved in the immediate years that followed the rituximab approval, the last decade saw a wave of antibody-drug approvals in the oncology arena. In the last three years, the EMA and FDA greenlighted eighteen antibodies, the majority of them designed in the formats of antibody-drug conjugates (ADC) and bispecific antibodies (BsAb). While the use of ADC and BsAb formats and the current rapid pace of approvals appear routine and almost inevitable, such progress was thought to be quite improbable in the early days of therapeutic antibody development. To understand how we arrived at the current state of antibody development in oncology, we focus on six monumental events that shaped antibody approvals over the last two and half decades. We examine the circumstances that led to the approval of rituximab and trastuzumab, the first successful antibodies for the treatment of hematologic and solid cancers. We detail the generation of the ADC and BsAb formats that dramatically augmented antibody-mediated precision cytotoxicity. Finally, we explore the development of ipilimumab, the first immune checkpoint-inhibiting antibody that activates the immune system to kill cancer cells, and the discovery that allowed the use of checkpoint inhibitors across all cancer types based on the presence of genetic markers. Revisiting these key events provides critical insights into the process of antibody development in oncology. |
format | Article |
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institution | Kabale University |
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language | English |
publishDate | 2025-02-01 |
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spelling | doaj-art-94685ff1e35b4f0bbd93f278f675e89b2025-02-10T05:16:12ZengFrontiers Media S.A.Frontiers in Immunology1664-32242025-02-011610.3389/fimmu.2025.15337961533796Six events that shaped antibody approvals in oncologySuman Paul0Suman Paul1Shibin Zhou2Shibin Zhou3Department of Oncology, Johns Hopkins School of Medicine, Baltimore, MD, United StatesLudwig Center for Cancer Genetics and Therapeutics, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, MD, United StatesDepartment of Oncology, Johns Hopkins School of Medicine, Baltimore, MD, United StatesLudwig Center for Cancer Genetics and Therapeutics, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, MD, United StatesA little over twenty-five years ago, the European Medicines Agency (EMA) and the Food and Drug Administration (FDA) approved the chimeric antibody rituximab which fundamentally altered the landscape of anti-cancer drugs. While only a few antibodies were approved in the immediate years that followed the rituximab approval, the last decade saw a wave of antibody-drug approvals in the oncology arena. In the last three years, the EMA and FDA greenlighted eighteen antibodies, the majority of them designed in the formats of antibody-drug conjugates (ADC) and bispecific antibodies (BsAb). While the use of ADC and BsAb formats and the current rapid pace of approvals appear routine and almost inevitable, such progress was thought to be quite improbable in the early days of therapeutic antibody development. To understand how we arrived at the current state of antibody development in oncology, we focus on six monumental events that shaped antibody approvals over the last two and half decades. We examine the circumstances that led to the approval of rituximab and trastuzumab, the first successful antibodies for the treatment of hematologic and solid cancers. We detail the generation of the ADC and BsAb formats that dramatically augmented antibody-mediated precision cytotoxicity. Finally, we explore the development of ipilimumab, the first immune checkpoint-inhibiting antibody that activates the immune system to kill cancer cells, and the discovery that allowed the use of checkpoint inhibitors across all cancer types based on the presence of genetic markers. Revisiting these key events provides critical insights into the process of antibody development in oncology.https://www.frontiersin.org/articles/10.3389/fimmu.2025.1533796/fullantibodyoncologybispecific antibody (bsAb)antibody drug conjugate (ADC)immune checkpoint inhibitor |
spellingShingle | Suman Paul Suman Paul Shibin Zhou Shibin Zhou Six events that shaped antibody approvals in oncology Frontiers in Immunology antibody oncology bispecific antibody (bsAb) antibody drug conjugate (ADC) immune checkpoint inhibitor |
title | Six events that shaped antibody approvals in oncology |
title_full | Six events that shaped antibody approvals in oncology |
title_fullStr | Six events that shaped antibody approvals in oncology |
title_full_unstemmed | Six events that shaped antibody approvals in oncology |
title_short | Six events that shaped antibody approvals in oncology |
title_sort | six events that shaped antibody approvals in oncology |
topic | antibody oncology bispecific antibody (bsAb) antibody drug conjugate (ADC) immune checkpoint inhibitor |
url | https://www.frontiersin.org/articles/10.3389/fimmu.2025.1533796/full |
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