Bevacizumab: Difference between revisions

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'''Bevacizumab''' is an "anti-VEGF ([http://www.ncbi.nlm.nih.gov/sites/entrez?db=protein&term=NP_001020537 Entrez protein]) monoclonal antibody consisting of humanized murine antibody with antigen-binding, complementary-determining regions from murine VEGF".<ref>{{MeSH|Bevacizumab [Substance Name]}}</ref>  In the United States, it is marketed as '''Avastin''' by [[Genentech]], a subsidiary of [[Roche Laboratories]].
'''Bevacizumab''' is an "anti-VEGF (i.e., [[vascular endothelial growth factor A]]([http://www.ncbi.nlm.nih.gov/sites/entrez?db=protein&term=NP_001020537 Entrez protein]) monoclonal antibody consisting of [[monoclonal antibody|humanized murine antibody]] with antigen-binding, complementary-determining regions from murine VEGF".<ref>{{MeSH|Bevacizumab [Substance Name]}}</ref>  In the United States, it is marketed as '''Avastin''' by [[Genentech]], a subsidiary of [[Roche Laboratories]] as an [[antineoplastic agent]].
==Indications==
==Indications==
The U.S. Food and Drug Administration (FDA) recognizes it as indicated for: [[glioma|glioblastoma multiforme]], metastatic [[breast cancer|breast carcinoma]], metastatic [[colorectal cancer]], [[lung cancer|non-small cell lung cancer]], and [[renal cell cardinoma]]. Common unlabeled uses are in [[astrocytoma|anaplastic astrocytoma]] and [[ovarian cardinoma]].  <ref name=Medscape-Intro>{{citation
The U.S. Food and Drug Administration (FDA) recognizes it as indicated for: [[glioma|glioblastoma multiforme]], metastatic [[breast cancer|breast carcinoma]], metastatic [[colorectal cancer]], [[lung cancer|non-small cell lung cancer]], and [[renal cell cardinoma]]. Common unlabeled uses are in [[astrocytoma|anaplastic astrocytoma]] and [[ovarian cardinoma]].  <ref name=Medscape-Intro>{{citation

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Bevacizumab is an "anti-VEGF (i.e., vascular endothelial growth factor A(Entrez protein) monoclonal antibody consisting of humanized murine antibody with antigen-binding, complementary-determining regions from murine VEGF".[1] In the United States, it is marketed as Avastin by Genentech, a subsidiary of Roche Laboratories as an antineoplastic agent.

Indications

The U.S. Food and Drug Administration (FDA) recognizes it as indicated for: glioblastoma multiforme, metastatic breast carcinoma, metastatic colorectal cancer, non-small cell lung cancer, and renal cell cardinoma. Common unlabeled uses are in anaplastic astrocytoma and ovarian cardinoma. [2]

Postmarketing review

It had received accelerated approval based on the surrogate marker that it decreased tumor size. On 16 July 2010, the FDA announced "FDA reviewers said two follow-up studies recently submitted by Roche failed to show that Avastin significantly extended lives compared to chemotherapy alone Additionally, the FDA said that in follow-up studies the drug did not slow tumor growth to the same degree as in earlier studies. Patients taking Avastin showed significantly more side effects, including high blood pressure, fatigue and abnormal white blood cell levels." [3]

References