Product review: avelumab, an anti-PD-L1 antibody

Although immunotherapies have been employed for many decades, immune checkpoint inhibitors have only recently entered the oncologic landscape. Avelumab is a fully human monoclonal antibody that blocks the interaction between PD-L1 on tumor cells and PD-1 on T cells, thereby inhibiting immunosuppress...

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Main Authors: Julie M. Collins, James L. Gulley
Format: Article
Language:English
Published: Taylor & Francis Group 2019-04-01
Series:Human Vaccines & Immunotherapeutics
Subjects:
Online Access:http://dx.doi.org/10.1080/21645515.2018.1551671
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author Julie M. Collins
James L. Gulley
author_facet Julie M. Collins
James L. Gulley
author_sort Julie M. Collins
collection DOAJ
description Although immunotherapies have been employed for many decades, immune checkpoint inhibitors have only recently entered the oncologic landscape. Avelumab is a fully human monoclonal antibody that blocks the interaction between PD-L1 on tumor cells and PD-1 on T cells, thereby inhibiting immunosuppression in the tumor microenvironment and reducing tumor growth. Most early clinical trials of avelumab as monotherapy and in combination regimens were part of the international JAVELIN clinical trial program, which included more than 7000 patients in more than 30 trials with at least 15 tumor types. Avelumab has been approved by the U.S. FDA for the treatment of metastatic Merkel cell carcinoma and metastatic urothelial carcinoma that has progressed during or following treatment with a platinum-based regimen. Its acceptable safety profile and ability to induce durable responses in otherwise deadly tumors provide the rationale for its use in other tumor types and in combination with other therapies.
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spelling doaj.art-eef4569b67f14718adf5d38981dec8902023-09-22T08:38:24ZengTaylor & Francis GroupHuman Vaccines & Immunotherapeutics2164-55152164-554X2019-04-0115489190810.1080/21645515.2018.15516711551671Product review: avelumab, an anti-PD-L1 antibodyJulie M. Collins0James L. Gulley1National Cancer Institute, National Institutes of HealthNational Cancer Institute, National Institutes of HealthAlthough immunotherapies have been employed for many decades, immune checkpoint inhibitors have only recently entered the oncologic landscape. Avelumab is a fully human monoclonal antibody that blocks the interaction between PD-L1 on tumor cells and PD-1 on T cells, thereby inhibiting immunosuppression in the tumor microenvironment and reducing tumor growth. Most early clinical trials of avelumab as monotherapy and in combination regimens were part of the international JAVELIN clinical trial program, which included more than 7000 patients in more than 30 trials with at least 15 tumor types. Avelumab has been approved by the U.S. FDA for the treatment of metastatic Merkel cell carcinoma and metastatic urothelial carcinoma that has progressed during or following treatment with a platinum-based regimen. Its acceptable safety profile and ability to induce durable responses in otherwise deadly tumors provide the rationale for its use in other tumor types and in combination with other therapies.http://dx.doi.org/10.1080/21645515.2018.1551671avelumabmonoclonal antibodyanti-pd-l1immune checkpoint inhibitorimmunotherapymsb0010718cmerkel cell carcinomaurothelial carcinoma
spellingShingle Julie M. Collins
James L. Gulley
Product review: avelumab, an anti-PD-L1 antibody
Human Vaccines & Immunotherapeutics
avelumab
monoclonal antibody
anti-pd-l1
immune checkpoint inhibitor
immunotherapy
msb0010718c
merkel cell carcinoma
urothelial carcinoma
title Product review: avelumab, an anti-PD-L1 antibody
title_full Product review: avelumab, an anti-PD-L1 antibody
title_fullStr Product review: avelumab, an anti-PD-L1 antibody
title_full_unstemmed Product review: avelumab, an anti-PD-L1 antibody
title_short Product review: avelumab, an anti-PD-L1 antibody
title_sort product review avelumab an anti pd l1 antibody
topic avelumab
monoclonal antibody
anti-pd-l1
immune checkpoint inhibitor
immunotherapy
msb0010718c
merkel cell carcinoma
urothelial carcinoma
url http://dx.doi.org/10.1080/21645515.2018.1551671
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