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ALT-803 in the treatment of non-muscle-invasive bladder cancer: Preclinical and clinical evidence and translational potential

Bladder cancer (BCa) is one of the most common malignant tumors that cause death. Approximately 75%–85% of BCa develop into non-muscle-invasive bladder cancer (NMIBC). Bacillus Calmette-Guérin (BCG) is the gold standard for avoiding cystectomy in the treatment of NMIBC. Unfortunately, up to 30% of p...

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Autores principales: Chen, Wujun, Liu, Ning, Yuan, Yang, Zhu, Meng, Hu, Xiaokun, Hu, Wenchao, Wang, Shuai, Wang, Chao, Huang, Binghuan, Xing, Dongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684637/
https://www.ncbi.nlm.nih.gov/pubmed/36439125
http://dx.doi.org/10.3389/fimmu.2022.1040669
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author Chen, Wujun
Liu, Ning
Yuan, Yang
Zhu, Meng
Hu, Xiaokun
Hu, Wenchao
Wang, Shuai
Wang, Chao
Huang, Binghuan
Xing, Dongming
author_facet Chen, Wujun
Liu, Ning
Yuan, Yang
Zhu, Meng
Hu, Xiaokun
Hu, Wenchao
Wang, Shuai
Wang, Chao
Huang, Binghuan
Xing, Dongming
author_sort Chen, Wujun
collection PubMed
description Bladder cancer (BCa) is one of the most common malignant tumors that cause death. Approximately 75%–85% of BCa develop into non-muscle-invasive bladder cancer (NMIBC). Bacillus Calmette-Guérin (BCG) is the gold standard for avoiding cystectomy in the treatment of NMIBC. Unfortunately, up to 30% of patients do not respond to BCG treatment, and up to 70% of BCG responders relapse. The United States Food and Drug Administration (FDA) approved valrubicin (1998) and pembrolizumab (2020) for the treatment of BCG-unresponsive (BCGu) NMBIC. However, the complete remission rate for valrubicin and pembrolizumab was only 16% and 40.6%, respectively. ALT-803 (N-803) is an IL-15 superagonist and reduces tumor burden by promoting the proliferation and activation of NK cells and CD8(+) T cells. The FDA received (23 May 2022) and accepted to review (28 July 2022) the marketing submission of ALT-803 plus BCG for the treatment of BCGu NMIBC. However, the FDA previously rejected the application for oportuzumab monatox (OM) due to a lack of data comparing it with pembrolizumab on August 20, 2021. Interestingly, the clinical efficacy and safety of ALT-803 were higher than that of pembrolizumab and OM, suggesting that ALT-803 may be approved by FDA. This review aims to further knowledge of the preclinical and clinical evidence of ALT-803 in the treatment of NMIBC and discuss its translational potential.
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spelling pubmed-96846372022-11-25 ALT-803 in the treatment of non-muscle-invasive bladder cancer: Preclinical and clinical evidence and translational potential Chen, Wujun Liu, Ning Yuan, Yang Zhu, Meng Hu, Xiaokun Hu, Wenchao Wang, Shuai Wang, Chao Huang, Binghuan Xing, Dongming Front Immunol Immunology Bladder cancer (BCa) is one of the most common malignant tumors that cause death. Approximately 75%–85% of BCa develop into non-muscle-invasive bladder cancer (NMIBC). Bacillus Calmette-Guérin (BCG) is the gold standard for avoiding cystectomy in the treatment of NMIBC. Unfortunately, up to 30% of patients do not respond to BCG treatment, and up to 70% of BCG responders relapse. The United States Food and Drug Administration (FDA) approved valrubicin (1998) and pembrolizumab (2020) for the treatment of BCG-unresponsive (BCGu) NMBIC. However, the complete remission rate for valrubicin and pembrolizumab was only 16% and 40.6%, respectively. ALT-803 (N-803) is an IL-15 superagonist and reduces tumor burden by promoting the proliferation and activation of NK cells and CD8(+) T cells. The FDA received (23 May 2022) and accepted to review (28 July 2022) the marketing submission of ALT-803 plus BCG for the treatment of BCGu NMIBC. However, the FDA previously rejected the application for oportuzumab monatox (OM) due to a lack of data comparing it with pembrolizumab on August 20, 2021. Interestingly, the clinical efficacy and safety of ALT-803 were higher than that of pembrolizumab and OM, suggesting that ALT-803 may be approved by FDA. This review aims to further knowledge of the preclinical and clinical evidence of ALT-803 in the treatment of NMIBC and discuss its translational potential. Frontiers Media S.A. 2022-11-10 /pmc/articles/PMC9684637/ /pubmed/36439125 http://dx.doi.org/10.3389/fimmu.2022.1040669 Text en Copyright © 2022 Chen, Liu, Yuan, Zhu, Hu, Hu, Wang, Wang, Huang and Xing https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Chen, Wujun
Liu, Ning
Yuan, Yang
Zhu, Meng
Hu, Xiaokun
Hu, Wenchao
Wang, Shuai
Wang, Chao
Huang, Binghuan
Xing, Dongming
ALT-803 in the treatment of non-muscle-invasive bladder cancer: Preclinical and clinical evidence and translational potential
title ALT-803 in the treatment of non-muscle-invasive bladder cancer: Preclinical and clinical evidence and translational potential
title_full ALT-803 in the treatment of non-muscle-invasive bladder cancer: Preclinical and clinical evidence and translational potential
title_fullStr ALT-803 in the treatment of non-muscle-invasive bladder cancer: Preclinical and clinical evidence and translational potential
title_full_unstemmed ALT-803 in the treatment of non-muscle-invasive bladder cancer: Preclinical and clinical evidence and translational potential
title_short ALT-803 in the treatment of non-muscle-invasive bladder cancer: Preclinical and clinical evidence and translational potential
title_sort alt-803 in the treatment of non-muscle-invasive bladder cancer: preclinical and clinical evidence and translational potential
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684637/
https://www.ncbi.nlm.nih.gov/pubmed/36439125
http://dx.doi.org/10.3389/fimmu.2022.1040669
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