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SGN-B6A: A New Vedotin Antibody–Drug Conjugate Directed to Integrin Beta-6 for Multiple Carcinoma Indications

Integrin beta-6, a component of the heterodimeric adhesion receptor alpha-v/beta-6, is overexpressed in numerous solid tumors. Its expression has been shown by multiple investigators to be a negative prognostic indicator in diverse cancers including colorectal, non–small cell lung, gastric, and cerv...

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Autores principales: Lyon, Robert P., Jonas, Mechthild, Frantz, Christopher, Trueblood, Esther S., Yumul, Roma, Westendorf, Lori, Hale, Christopher J., Stilwell, Jackie L., Yeddula, Narayana, Snead, Katie M., Kumar, Vineet, Patilea-Vrana, Gabriela I., Klussman, Kerry, Ryan, Maureen C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for Cancer Research 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690100/
https://www.ncbi.nlm.nih.gov/pubmed/37619980
http://dx.doi.org/10.1158/1535-7163.MCT-22-0817
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author Lyon, Robert P.
Jonas, Mechthild
Frantz, Christopher
Trueblood, Esther S.
Yumul, Roma
Westendorf, Lori
Hale, Christopher J.
Stilwell, Jackie L.
Yeddula, Narayana
Snead, Katie M.
Kumar, Vineet
Patilea-Vrana, Gabriela I.
Klussman, Kerry
Ryan, Maureen C.
author_facet Lyon, Robert P.
Jonas, Mechthild
Frantz, Christopher
Trueblood, Esther S.
Yumul, Roma
Westendorf, Lori
Hale, Christopher J.
Stilwell, Jackie L.
Yeddula, Narayana
Snead, Katie M.
Kumar, Vineet
Patilea-Vrana, Gabriela I.
Klussman, Kerry
Ryan, Maureen C.
author_sort Lyon, Robert P.
collection PubMed
description Integrin beta-6, a component of the heterodimeric adhesion receptor alpha-v/beta-6, is overexpressed in numerous solid tumors. Its expression has been shown by multiple investigators to be a negative prognostic indicator in diverse cancers including colorectal, non–small cell lung, gastric, and cervical. We developed SGN-B6A as an antibody–drug conjugate (ADC) directed to integrin beta-6 to deliver the clinically validated payload monomethyl auristatin E (MMAE) to cancer cells. The antibody component of SGN-B6A is specific for integrin beta-6 and does not bind other alpha-v family members. In preclinical studies, this ADC has demonstrated activity in vivo in models derived from non–small cell lung, pancreatic, pharyngeal, and bladder carcinomas spanning a range of antigen expression levels. In nonclinical toxicology studies in cynomolgus monkeys, doses of up to 5 mg/kg weekly for four doses or 6 mg/kg every 3 weeks for two doses were tolerated. Hematologic toxicities typical of MMAE ADCs were dose limiting, and no significant target-mediated toxicity was observed. A phase I first-in-human study is in progress to evaluate the safety and antitumor activity of SGN-B6A in a variety of solid tumors known to express integrin beta-6 (NCT04389632).
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spelling pubmed-106901002023-12-02 SGN-B6A: A New Vedotin Antibody–Drug Conjugate Directed to Integrin Beta-6 for Multiple Carcinoma Indications Lyon, Robert P. Jonas, Mechthild Frantz, Christopher Trueblood, Esther S. Yumul, Roma Westendorf, Lori Hale, Christopher J. Stilwell, Jackie L. Yeddula, Narayana Snead, Katie M. Kumar, Vineet Patilea-Vrana, Gabriela I. Klussman, Kerry Ryan, Maureen C. Mol Cancer Ther Large Molecule Therapeutics Integrin beta-6, a component of the heterodimeric adhesion receptor alpha-v/beta-6, is overexpressed in numerous solid tumors. Its expression has been shown by multiple investigators to be a negative prognostic indicator in diverse cancers including colorectal, non–small cell lung, gastric, and cervical. We developed SGN-B6A as an antibody–drug conjugate (ADC) directed to integrin beta-6 to deliver the clinically validated payload monomethyl auristatin E (MMAE) to cancer cells. The antibody component of SGN-B6A is specific for integrin beta-6 and does not bind other alpha-v family members. In preclinical studies, this ADC has demonstrated activity in vivo in models derived from non–small cell lung, pancreatic, pharyngeal, and bladder carcinomas spanning a range of antigen expression levels. In nonclinical toxicology studies in cynomolgus monkeys, doses of up to 5 mg/kg weekly for four doses or 6 mg/kg every 3 weeks for two doses were tolerated. Hematologic toxicities typical of MMAE ADCs were dose limiting, and no significant target-mediated toxicity was observed. A phase I first-in-human study is in progress to evaluate the safety and antitumor activity of SGN-B6A in a variety of solid tumors known to express integrin beta-6 (NCT04389632). American Association for Cancer Research 2023-12-01 2023-08-24 /pmc/articles/PMC10690100/ /pubmed/37619980 http://dx.doi.org/10.1158/1535-7163.MCT-22-0817 Text en ©2023 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license.
spellingShingle Large Molecule Therapeutics
Lyon, Robert P.
Jonas, Mechthild
Frantz, Christopher
Trueblood, Esther S.
Yumul, Roma
Westendorf, Lori
Hale, Christopher J.
Stilwell, Jackie L.
Yeddula, Narayana
Snead, Katie M.
Kumar, Vineet
Patilea-Vrana, Gabriela I.
Klussman, Kerry
Ryan, Maureen C.
SGN-B6A: A New Vedotin Antibody–Drug Conjugate Directed to Integrin Beta-6 for Multiple Carcinoma Indications
title SGN-B6A: A New Vedotin Antibody–Drug Conjugate Directed to Integrin Beta-6 for Multiple Carcinoma Indications
title_full SGN-B6A: A New Vedotin Antibody–Drug Conjugate Directed to Integrin Beta-6 for Multiple Carcinoma Indications
title_fullStr SGN-B6A: A New Vedotin Antibody–Drug Conjugate Directed to Integrin Beta-6 for Multiple Carcinoma Indications
title_full_unstemmed SGN-B6A: A New Vedotin Antibody–Drug Conjugate Directed to Integrin Beta-6 for Multiple Carcinoma Indications
title_short SGN-B6A: A New Vedotin Antibody–Drug Conjugate Directed to Integrin Beta-6 for Multiple Carcinoma Indications
title_sort sgn-b6a: a new vedotin antibody–drug conjugate directed to integrin beta-6 for multiple carcinoma indications
topic Large Molecule Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690100/
https://www.ncbi.nlm.nih.gov/pubmed/37619980
http://dx.doi.org/10.1158/1535-7163.MCT-22-0817
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