US2003134344A1PendingUtilityA1

Gene detection assay for improving the likelihood of an effective response to an ErbB antagonist cancer therapy

Assignee: GENENTECH INCPriority: May 19, 2000Filed: Oct 30, 2002Published: Jul 17, 2003
Est. expiryMay 19, 2020(expired)· nominal 20-yr term from priority
Inventors:Robert D. Mass
A61P 43/00A61P 37/04A61P 35/02A61P 35/00A61P 15/00A61P 15/14C12Q 2600/106A61K 31/335A61K 39/39558G01N 33/5023C07K 2317/24A61K 38/00C12Q 1/6886C07K 16/40A61K 31/337C07K 16/2863A61K 48/00C12Q 1/6841C12Q 2600/158A61K 2300/00C07K 16/32G01N 33/57515
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Claims

Abstract

The invention provides a method for more effective treatment of patients susceptible to or diagnosed with tumors overexpressing ErbB, as determined by a gene amplification assay, with an ErbB antagonist. Such method comprises administering a cancer-treating dose of the ErbB antagonist, preferably in addition to chemotherapeutic agents, to a subject in whose tumor cells ErbB has been found to be amplified e.g., by fluorescent in situ hybridization. ErbB antagonists described include an anti-HER2 antibody. Pharmaceutical packaging for providing the components for such treatment is also provided.

Claims

exact text as granted — not AI-modified
What is claimed:  
     
         1 . A method for increasing likelihood of effectiveness of an ErbB antagonist cancer treatment, which method comprises administering a cancer treating dose of the ErbB antagonist to a subject, wherein an erbB gene in tumor cells in a tissue sample from the subject has been found to be amplified.  
     
     
         2 . The method according to  claim 1 , wherein the ErbB is a HER2 protein.  
     
     
         3 . The method according to  claim 2 , wherein the cancer is breast cancer.  
     
     
         4 . The method according to  claim 3 , wherein the subject has been found to have a 0 or 1+ score by immunohistochemistry on a formaldehyde-fixed tissue sample.  
     
     
         5 . The method according to  claim 1 , wherein the ErbB antagonist is an anti-ErbB antibody.  
     
     
         6 . The method according to  claim 5 , wherein the ErbB is HER2, and the antibody is recombinant human monoclonal antibody (rhuMAb) 4D5.  
     
     
         7 . The method according to  claim 1 , wherein the erbB gene amplification is detected by detecting fluorescence of a fluorescent-labeled nucleic acid probe hybridized to the gene.  
     
     
         8 . The method according to  claim 7 , wherein the erbB gene is a her2 gene..  
     
     
         9 . The method according to  claim 1 , which further comprises administering a cancer treating dose of a chemotherapeutic drug.  
     
     
         10 . The method according to  claim 9 , wherein the ErbB is HER2 and the chemotherapeutic drug is a taxoid.  
     
     
         11 . The method according to claim I, wherein the likelihood of effectiveness increases by about 30%.  
     
     
         12 . A method for increasing likelihood of effectiveness of an anti-HER2 antibody to treat cancer, which method comprises administering a cancer treating dose of the anti-HER2 antibody to the subject, wherein a her2 gene in tumor cells in a tissue sample from the subject have been found to be amplified.  
     
     
         13 . The method according to  claim 12 , wherein the subject has been found to have a 0 or 1+ score by immunohistochemistry on a formaldehyde-fixed tissue sample.  
     
     
         14 . The method according to  claim 12 , which further comprises administering a cancer treating dose of a taxoid.

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