<?xml version="1.0" encoding="UTF-8"?>
<oaidc:dc xmlns:oaidc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:coverage xsi:type="unistra:Coverage">FR</dc:coverage>
<dc:creator xsi:type="unistra:Auteur">Rakotoary, Tatamo</dc:creator>
<dc:date xsi:type="unistra:Date">2023-11-24</dc:date>
<dc:description xsi:type="unistra:Discipline" xml:langue="fre">Pharmacie</dc:description>
<dc:description xsi:type="unistra:Resume" xml:langue="fre">Les anticorps bispécifiques sont des traitements en plein essor dans l’immunothérapie anticancéreuse. Ils se catégorisent en 3 classes : les anticorps engageant des cellules cytotoxiques (LT ou NK), les immunomodulateurs dirigés contre les tumeurs et les immunomodulateurs doubles. La plupart de ces anticorps ont été conçus pour se positionner dans la prise en charge de stades ou de types de cancers encore difficilement curables, avec la promesse de pallier les limitations des traitement actuels. La revue des résultats d’études cliniques portant sur différents anticorps issus de ces 3 classes, nous permet de conclure que, globalement, leur profil de sécurité est prédictible et gérable, et que ces anticorps présentent déjà des prémices d’une efficacité antitumorale qui pourrait être bénéfique pour les patients cancéreux.</dc:description>
<dc:description xsi:type="unistra:Resume" xml:langue="fre">Bispecific antibodies are a fast-growing field of cancer immunotherapy. They are classified into 3 classes: cytotoxic effector cell redirectors (T-cells or NK redirectors), tumor-targeted immunomodulators and dual immunomodulators. Most of these antibodies have been designed for the treatment of stages or types of cancers that are still difficult to cure, with the promise of overcoming the limitations of current treatments. A review of the clinical studies results on various antibodies from these 3 classes leads us to conclude that, overall, their safety profile is predictable and manageable, and that these antibodies are already showing some antitumor efficacy that could benefit cancer patients.</dc:description>
<dc:format xsi:type="dcterms:IMT">PDF</dc:format>
<dc:rights xsi:type="unistra:Droits" xml:lang="fre">Accès libre</dc:rights>
<dc:identifier xsi:type="dcterms:URI">https://publication-theses.unistra.fr/public/theses_exercice/PHA/2023/2023_RAKOTOARY_Tatamo.pdf</dc:identifier>
<dc:language xsi:type="dcterms:ISO639-2">fr</dc:language>
<dc:source xsi:type="dcterms:URI">http://www.sudoc.fr/27381463X</dc:source>
<dc:subject xml:langue="fre">Immunothérapie anticancéreuse</dc:subject>
<dc:subject xml:langue="fre">Anticorps bispécifiques</dc:subject>
<dc:subject xml:langue="fre">Immunothérapie anticancéreuse</dc:subject>
<dc:subject xml:langue="fre">Anticorps bispécifiques</dc:subject>
<dc:subject xml:langue="fre">Etudes cliniques</dc:subject>
<dc:subject xml:langue="fre">Binatumomab</dc:subject>
<dc:subject xml:langue="fre">Cevostamab</dc:subject>
<dc:subject xml:langue="fre">Mosunetuzumab</dc:subject>
<dc:subject xml:langue="fre">Glofitamab</dc:subject>
<dc:subject xml:langue="fre">Tobemstomig</dc:subject>
<dc:subject xml:langue="fre">Cancer immunotherapy</dc:subject>
<dc:subject xml:langue="fre">Bispecific antibodies</dc:subject>
<dc:subject xml:langue="fre">Clinical trials</dc:subject>
<dc:subject xml:langue="fre">Blinatumomab</dc:subject>
<dc:subject xml:langue="fre">Cevostamab</dc:subject>
<dc:subject xml:langue="fre">Mosunetuzumab</dc:subject>
<dc:subject xml:langue="fre">Glofitamab</dc:subject>
<dc:subject xml:langue="fre">Tobemstomig</dc:subject>
<dc:subject xml:langue="fre">610</dc:subject>
<dc:title xsi:type="unistra:Titre" xml:lang="fre">Les anticorps bispécifiques dans l'immunothérapie anticancéreuse</dc:title>
<dc:type xsi:type="unistra:Mention">Thèse d'exercice</dc:type>
<dc:publisher xsi:type="unistra:Composante">Faculté de pharmacie</dc:publisher>
<dc:contributor xsi:type="unistra:Directeur">Pauline Soulas-Sprauel</dc:contributor>
<dc:type xsi:type="unistra:TheseExercice">These d'exercice Unistra</dc:type>
</oaidc:dc>
