Your browser doesn't support javascript.
loading
AMG 595, an Anti-EGFRvIII Antibody-Drug Conjugate, Induces Potent Antitumor Activity against EGFRvIII-Expressing Glioblastoma.
Hamblett, Kevin J; Kozlosky, Carl J; Siu, Sophia; Chang, Wesley S; Liu, Hua; Foltz, Ian N; Trueblood, Esther S; Meininger, David; Arora, Taruna; Twomey, Brian; Vonderfecht, Steven L; Chen, Qing; Hill, John S; Fanslow, William C.
Afiliación
  • Hamblett KJ; Amgen Inc., Seattle, Washington. kjhamblett@comcast.net.
  • Kozlosky CJ; Amgen Inc., Seattle, Washington.
  • Siu S; Amgen Inc., Seattle, Washington.
  • Chang WS; Amgen Inc., South San Francisco, California.
  • Liu H; Amgen Inc., Seattle, Washington.
  • Foltz IN; Amgen Inc., Burnaby, British Columbia, Canada.
  • Trueblood ES; Amgen Inc., Seattle, Washington.
  • Meininger D; Amgen Inc., Seattle, Washington.
  • Arora T; Amgen Inc., Thousand Oaks, California.
  • Twomey B; Amgen Inc., Thousand Oaks, California.
  • Vonderfecht SL; Amgen Inc., Thousand Oaks, California.
  • Chen Q; Amgen Inc., Thousand Oaks, California.
  • Hill JS; Amgen Inc., Thousand Oaks, California.
  • Fanslow WC; Amgen Inc., Seattle, Washington.
Mol Cancer Ther ; 14(7): 1614-24, 2015 Jul.
Article en En | MEDLINE | ID: mdl-25931519
Epidermal growth factor receptor variant III (EGFRvIII) is a cancer-specific deletion mutant observed in approximately 25% to 50% of glioblastoma multiforme (GBM) patients. An antibody drug conjugate, AMG 595, composed of the maytansinoid DM1 attached to a highly selective anti-EGFRvIII antibody via a noncleavable linker, was developed to treat EGFRvIII-positive GBM patients. AMG 595 binds to the cell surface and internalizes into the endo-lysosomal pathway of EGFRvIII-expressing cells. Incubation of AMG 595 with U251 cells expressing EGFRvIII led to potent growth inhibition. AMG 595 treatment induced significant tumor mitotic arrest, as measured by phospho-histone H3, in GBM subcutaneous xenografts expressing EGFRvIII. A single intravenous injection of AMG 595 at 17 mg/kg (250 µg DM1/kg) generated complete tumor regression in the U251vIII subcutaneous xenograft model. AMG 595 mediated tumor regression in the D317 subcutaneous xenograft model that endogenously expresses EGFRvIII. Finally, AMG 595 treatment inhibited the growth of D317 xenografts orthotopically implanted into the brain as determined by magnetic resonance imaging. These results demonstrate that AMG 595 is a promising candidate to evaluate in EGFRvIII-expressing GBM patients.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma / Inmunoconjugados / Ensayos Antitumor por Modelo de Xenoinjerto / Receptores ErbB / Anticuerpos Monoclonales Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans Idioma: En Revista: Mol Cancer Ther Asunto de la revista: ANTINEOPLASICOS Año: 2015 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma / Inmunoconjugados / Ensayos Antitumor por Modelo de Xenoinjerto / Receptores ErbB / Anticuerpos Monoclonales Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans Idioma: En Revista: Mol Cancer Ther Asunto de la revista: ANTINEOPLASICOS Año: 2015 Tipo del documento: Article Pais de publicación: Estados Unidos