Anti-EGFRvIII antibodies and uses thereof
The present invention provides antibodies that bind to the class III variant of EGFR (EGFRvIII) and methods of using the same. According to certain embodiments, the antibodies of the invention bind human EGFRvIII with high affinity. The antibodies of the invention may be fully human antibodies. The invention includes anti-EGFRvIII antibodies conjugated to a cytotoxic agent, radionuclide, or other moiety detrimental to cell growth or proliferation. The antibodies of the invention are useful for the treatment of various cancers.
1. A method for treating a cancer or tumor expressing EGFRvIII, comprising administering to a subject in need thereof a therapeutically effective amount of a pharmaceutical composition comprising an isolated antibody or antigen-binding fragment thereof that specifically binds human EGFRvIII, but binds neither the junctional peptide of SEQ ID NO:148 nor the peptide of SEQ ID NO:165, wherein the antibody comprises the complementarity determining regions (CDRs) within the heavy chain variable region/light chain variable region (HCVR/LCVR) amino acid sequence pair of SEQ ID NOs: 34/42, and a pharmaceutically acceptable carrier,
wherein the cancer or tumor growth is inhibited.
2. The method of claim 1 , wherein the cancer or tumor is selected from the group consisting of glioblastoma, ductal or intraductal breast carcinoma, non-small cell lung carcinomas, ovarian carcinomas, prostate cancer, and squamous cell carcinoma of the head and neck.
3. The method of claim 1 , further comprising treating the subject with one or more additional therapeutic agents selected from the group consisting of a chemotherapeutic agent, anti-inflammatory agents, and analgesics.
4. The method of claim 1 , wherein the HCVR comprises an amino acid sequence of SEQ ID NO: 34.
5. The method of claim 1 , wherein the LCVR comprises an amino acid sequence of SEQ ID NO: 42.
6. The method of claim 1 , wherein the antibody or antigen-binding fragment comprises a HCVR/LCVR sequence pair of SEQ ID NO: 34/42.
7. The method of claim 1 , wherein the antibody or antigen-binding fragment is conjugated to a cytotoxin.
8. The method of claim 7 , wherein the cytotoxin is selected from the group consisting of biotoxins, chemotherapeutic agents and radioisotopes.
9. The method of claim 7 , wherein the cytotoxin is selected from the group consisting of maytansinoids, auristatins, tomaymycins, duocarmycins, 225Ac, 227Th, and any derivatives thereof.
10. The method of claim 9 , wherein the antibody or antigen-binding fragment is conjugated to a maytansinoid.
11. A method for treating a cancer, reducing tumor growth and/or causing tumor regression in a patient, the method comprising administering to a patient in need thereof a first antibody-drug conjugate (ADC) comprising an antibody or antigen-binding fragment thereof wherein the antibody comprises the CDRs within the HCVR/LCVR amino acid sequence pair of SEQ ID NOs: 34/42, and a cytotoxin,
wherein the antibody or antigen-binding fragment of the first ADC specifically binds EGFRvIII but binds neither the junctional peptide of SEQ ID NO:148 nor the peptide of SEQ ID NO:165,
wherein the cancer or tumor growth is inhibited or the tumor regresses.
12. The method of claim 11 , wherein the method further comprises administering to the patient a second ADC comprising an antibody or antigen-binding fragment thereof and a cytotoxin, wherein the antibody or antigen-binding fragment of the second ADC specifically binds EGFRvIII and also binds the junctional peptide of SEQ ID NO:148 and/or the peptide of SEQ ID NO:165.
13. The method of claim 11 , wherein the antibody or antigen-binding fragment of the first ADC comprises a heavy chain variable region comprising SEQ ID NO: 34 and a light chain variable region comprising SEQ ID NO: 42.