Treatment method using EGFR antibodies and SRC inhibitors and related formulations
The present invention relates to the treatment of EGFR-mediated disease, particularly cancer by inhibiting or blocking EGFR and src in combination or simultaneously. The invention relates to treatment, prevention, or modulation of cancer, particularly EGFR-mediated disease, with one or more EGFR modulator and src inhibitor in combination. The invention further relates to the treatment of cancer with anti-EGFR antibodies and src inhibitors. Methods and compositions for treatment of cancer with the antibody anti-EGFR mAb806 in combination or series with a src inhibitor or src inhibitors are described.
1. A method of treating glioblastoma in a human, comprising administering to said human the src inhibitor dasatinib (BMS354825) and the anti-EGFR antibody mAb806 or an antigen-binding fragment thereof, wherein said src inhibitor dasatinib (BMS354825) and said anti-EGFR antibody mAb806 or antigen-binding fragment thereof are administered to said human simultaneously, in combination, or one after another in series, and wherein the glioblastoma is characterized by EGFR over-expression or an EGFR mutation.
2. A method for blocking or reducing tumor growth of glioblastoma in a human, comprising administering to said human the src inhibitor dasatinib (BMS354825) and the anti-EGFR antibody mAb806 or an antigen-binding fragment thereof, wherein said src inhibitor dasatinib (BMS354825) and said anti-EGFR antibody mAb806 or antigen-binding fragment thereof are administered to said human simultaneously, in combination, or one after another series, and wherein the glioblastoma is characterized by EGFR over-expression or an EGFR mutation.
3. A method of enhancing the effectiveness or activity of the anti-EGFR antibody mAb806 or an antigen-binding fragment thereof in a human with glioblastoma, comprising administering to said human a combination of the anti-EGFR antibody mAb806 or an antigen-binding fragment thereof and the src inhibitor dasatinib (BMS354825), and wherein the glioblastoma is characterized by EGFR over-expression or an EGFR mutation.
4. A method of treating glioblastoma in a human according to claim 1 , wherein said antigen-binding fragment is Fab or F(ab′) 2 .
5. A method for blocking or reducing tumor growth of glioblastoma in a human according to claim 2 , wherein said antigen-binding fragment is Fab or F(ab′) 2 .
6. A method of enhancing the effectiveness or activity of the anti-EGFR antibody mAb806 or an antigen-binding fragment thereof in a human according to claim 3 , wherein said antigen-binding fragment is Fab or F(ab′) 2 .
7. The method of any one of claim 1 , 2 or 3 wherein the EGFR mutation is a de2-7 EGFR mutation.
8. The method of any one of claim 1 , 2 or 3 , wherein mAb806 is a chimeric or humanized antibody.
9. The method of any one of claim 1 , 2 or 3 , wherein mAb806 is labeled with a detectable or functional label.
10. The method of claim 9 , wherein the detectable or functional label is covalently attached.
11. The method of claim 9 , wherein the functional label is selected from the group consisting of a chemical ablation agent, toxin, immunomodulator, cytokine, cytotoxic agent, chemotherapeutic agent and drug.
12. The method of claim 9 , wherein the functional label is a toxin.
13. The method of claim 9 , wherein the functional label is a cytotoxic agent.
14. The method of claim 9 , wherein the detectable label is a radiolabel.