Methods of treating cancer

Abstract

Provided are methods of treating cancer (e.g., non-small cell lung cancer (NSCLC), head and neck squamous cell carcinoma (HNSCC), HER2-positive gastric/gastroesophageal junction (GEJ) cancer, de novo or transformed diffuse large B cell lymphoma (DLBCL), or indolent lymphoma) in an individual that comprise administering to the individual (a) a polypeptide comprising a SIRPα D1 domain variant and an Fc domain variant, and (b) an anti-cancer antibody (e.g., an anti-PD1 antibody, anti-HER2 antibody, or an anti-CD20 antibody). Also provided are related kits pharmaceutical compositions.

1 - 9 . (canceled) 
     
     
         10 . A method of treating HER2-positive gastric/gastroesophageal junction (GEJ) cancer in an individual, comprising administering to the individual an effective amount of (a) a polypeptide comprising a SIRPα D1 domain variant and an Fc domain variant, and (b) an anti-HER2 antibody,
 wherein the SIRPα D1 domain variant comprises the amino acid sequence of SEQ ID NO: 81 or SEQ ID NO: 85; 
 wherein the Fc domain variant is
 (i) a human IgG1 Fc region comprising L234A, L235A, G237A, and N297A mutations, wherein numbering is according to the EU index of Kabat; 
 (ii) a human IgG2 Fc region comprising A330S, P331S, and N297A mutations, wherein numbering is according to the EU index of Kabat; 
 (iii) a human IgG4 Fc region comprising S228P, E233P, F234V, L235A, and delG236 mutations, wherein numbering is according to the EU index of Kabat; or 
 (iv) a human IgG4 Fc region comprising S228P, E233P, F234V, L235A, delG236, and N297A mutations, wherein numbering is according to the EU index of Kabat; and 
 
 wherein the gastric/GEJ cancer in the individual has progressed following a prior treatment with a fluoropyrimidine-based therapy and/or a prior treatment with an anti-HER2 antibody, and wherein the individual is a human. 
 
     
     
         11 . The method of  claim 10 , wherein the prior treatment with the fluoropyrimidine-based therapy or the prior treatment with the anti-HER2 antibody comprised one or more therapeutic agents selected from the group consisting of: trastuzumab, pertuzumab, 5-fluorouracil, capecitabine, margetuximab, and FOLFOX. 
     
     
         12 . The method of  claim 10 , wherein the anti-HER2 antibody is trastuzumab. 
     
     
         13 . The method of  claim 12 , wherein trastuzumab is administered to the individual at an initial dose of 8 mg/kg and at a dose of 6 mg/kg for each subsequent dose, and wherein trastuzumab is administered to the individual by IV infusion every 3 weeks (Q3W). 
     
     
         14 - 24 . (canceled) 
     
     
         25 . The method of  claim 10 , wherein the SIRPα D1 domain variant comprises the amino acid sequence of SEQ ID NO: 85. 
     
     
         26 . The method of  claim 10 , wherein the SIRPα D1 domain variant comprises the amino acid sequence of SEQ ID NO: 81. 
     
     
         27 . The method of  claim 10 , wherein the Fc domain variant is a human IgG1 Fc region comprising L234A, L235A, G237A, and N297A mutations, wherein numbering is according to the EU index of Kabat. 
     
     
         28 . The method of  claim 27 , wherein the Fc domain variant comprises the amino acid sequence of SEQ ID NO: 91. 
     
     
         29 . The method of  claim 10 , wherein the polypeptide comprising a SIRPα D1 domain variant and an Fc domain variant comprises the amino acid sequence of SEQ ID NO: 136. 
     
     
         30 . The method of  claim 10 , wherein the polypeptide comprising a SIRPα D1 domain variant and an Fc domain variant comprises the amino acid sequence of SEQ ID NO: 135. 
     
     
         31 . The method of  claim 10 , wherein the polypeptide comprising a SIRPα D1 domain variant and an Fc domain variant forms a homodimer. 
     
     
         32 . The method  claim 10 , wherein the polypeptide comprising a SIRPα D1 domain variant and an Fc domain variant is administered to the individual at a dose of 10 mg/kg once per week (QW). 
     
     
         33 . (canceled) 
     
     
         34 . The method of  claim 32 , wherein the polypeptide comprising a SIRPα D1 domain variant and an Fc domain variant is administered to the individual by IV infusion. 
     
     
         35 - 58 . (canceled)