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A randomized adaptive phase II/III study of buparlisib, a pan-class I PI3K inhibitor, combined with paclitaxel for the treatment of HER2- advanced breast cancer (BELLE-4).

Identifieur interne : 001270 ( Main/Exploration ); précédent : 001269; suivant : 001271

A randomized adaptive phase II/III study of buparlisib, a pan-class I PI3K inhibitor, combined with paclitaxel for the treatment of HER2- advanced breast cancer (BELLE-4).

Auteurs : M. Martín [Espagne] ; A. Chan [Australie] ; L. Dirix [Belgique] ; J. O'Shaughnessy [États-Unis] ; R. Hegg [Brésil] ; A. Manikhas [Russie] ; M. Shtivelband [États-Unis] ; P. Krivorotko [Russie] ; N. Batista L Pez [Espagne] ; M. Campone [France] ; M. Ruiz Borrego [Espagne] ; Q J Khan ; J T Beck [États-Unis] ; M. Ramos Vázquez [Espagne] ; P. Urban [Suisse] ; S. Goteti ; E. Di Tomaso [États-Unis] ; C. Massacesi [France] ; S. Delaloge [France]

Source :

RBID : pubmed:27803006

Abstract

Phosphatidylinositol 3-kinase (PI3K) pathway activation in preclinical models of breast cancer is associated with tumor growth and resistance to anticancer therapies, including paclitaxel. Effects of the pan-Class I PI3K inhibitor buparlisib (BKM120) appear synergistic with paclitaxel in preclinical and clinical models.

DOI: 10.1093/annonc/mdw562
PubMed: 27803006


Affiliations:


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<div type="abstract" xml:lang="en">Phosphatidylinositol 3-kinase (PI3K) pathway activation in preclinical models of breast cancer is associated with tumor growth and resistance to anticancer therapies, including paclitaxel. Effects of the pan-Class I PI3K inhibitor buparlisib (BKM120) appear synergistic with paclitaxel in preclinical and clinical models.</div>
</front>
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<li>Belgique</li>
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<li>Suisse</li>
<li>États-Unis</li>
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<li>Île-de-France</li>
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<li>Paris</li>
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<name sortKey="O Shaughnessy, J" sort="O Shaughnessy, J" uniqKey="O Shaughnessy J" first="J" last="O'Shaughnessy">J. O'Shaughnessy</name>
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<name sortKey="Massacesi, C" sort="Massacesi, C" uniqKey="Massacesi C" first="C" last="Massacesi">C. Massacesi</name>
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