Combination therapies comprising anti-ERBB3 agents
Disclosed are methods and compositions for inhibiting the growth of a tumor (e.g., a malignant tumor) in a subject. In particular, combination therapies for treating a tumor in a subject by co-administering an agent selected from i) an effective amount of an anti-estrogen agent; ii) an effective amount of a receptor tyrosine kinase inhibitor; iii) an effective amount of a MEK/PI3 kinase/AKT inhibitor; iv) an effective amount of MM-151; v) an effective amount of an mTOR inhibitor; and/or vi) an effective amount of trastuzumab or TMD1, and/or combinations thereof; and an effective amount of a bispecific anti-ErbB2/anti-ErbB3 antibody. Also disclosed is a bispecific anti-ErbB2/anti-ErbB3 antibody for use in the therapy of a tumor in combination with an agent selected from i) an effective amount of an anti-estrogen agent; ii) an effective amount of a receptor tyrosine kinase inhibitor; iii) an effective amount of a MEK/PI3 kinase/AKT inhibitor; iv) an effective amount of MM-151; v) an effective amount of an mTOR inhibitor; and/or vi) an effective amount of trastuzumab or TMD1, and/or combinations thereof.
1. A method of treating a subject with a malignant tumor, the method comprising co-administering to the subject an effective amount of trametinib and a bispecific anti-ErbB2/anti-ErbB3 antibody that inhibits heregulin activation of ErbB2 and ErbB3 and, optionally, an effective amount of trastuzumab or ado-trastuzumab emtansine, wherein the co-administration to the subject creates a substantially superadditive effect.
2. The method of claim 1 , wherein the co-administration to the subject does not create a drug-drug interaction-mediated toxicity in the subject.
3. The method of claim 1 wherein the bispecific anti-ErbB2/anti-ErbB3 antibody comprises the amino acid sequence set forth in SEQ ID NO:1.
4. The method of claim 1 further comprising administering an effective amount of capecitabine and/or cisplatin.
5. The method of claim 1 , wherein the subject is a human.