TNF-alpha immunoconjugate therapy for the treatment of brain tumors

1. A method of treating a brain tumor in a patient, comprising administering a TNFα immunoconjugate in combination with chemotherapy to the patient, wherein the TNFα immunoconjugate comprises TNFα linked to an antibody molecule comprising L19 complementarity determining regions (CDRs), wherein the L19 CDRs are:

SEQ ID NO: 1

VH CDR1

SFSMS

SEQ ID NO: 2

VH CDR 2

SISGSSGTTYYADSVKG

SEQ ID NO: 3

VH CDR 3

PFPYFDY

SEQ ID NO: 4

VL CDR 1

RASQSVSSSFLA

SEQ ID NO: 5

VL CDR 2

YASSRAT, and

SEQ ID NO: 6

VL CDR 3

QQTGRIPPT;

and the chemotherapy is lomustine, wherein said combination increases brain tumor necrosis and Progression Free Survival (PFS) in said patient and said brain tumor is a glioma.

2. The method of claim 1 , wherein the antibody molecule comprises the L19 VH domain SEQ ID NO: 7 and the L19 VL domain SEQ ID NO: 9.

3. The method of 1 , wherein the TNFα immunoconjugate comprises TNFα linked to L19 (scFv) as set forth in SEQ ID NO: 10.

4. The method of any one of claim 1 , 2 , or 3 , wherein the TNFα immunoconjugate has an amino acid sequence of SEQ ID NO: 13.

5. The method of claim 1 , wherein the immunoconjugate is administered by a route selected from intravenous injection, intratumoural injection, and intrathecal injection.

6. The method of claim 1 , wherein the glioma is selected from a Grade III/IV glioma, a Grade III/IV glioma is at first relapse, an isocitrate dehydrogenase (IDH) wildtype glioma, a newly diagnosed Grade IV glioblastoma, and a Grade IV glioblastoma at first relapse.

7. The method of claim 1 , wherein the immunoconjugate is administered in combination with radiotherapy.

8. The method of claim 1 , wherein lomustine is administered at a dose in a range of 50-200 mg/m 2 , or 75-150 mg/m 2 .

9. The method of claim 1 , wherein the lomustine is administered at a dose of about 80, about 90, or about 100, or about 110 mg/m 2 .

10. The method of claim 1 , further comprising subsequent administrations of the TNFα immunoconjugate.

11. A method of treating a glioma in a patient, comprising administering a TNFα immunoconjugate in combination with chemotherapy to the patient, wherein the TNFα immunoconjugate comprises TNFα linked to an antibody molecule comprising L19 complementarity determining regions (CDRs), wherein the L19 CDRs are:

SEQ ID NO: 1

VH CDR1

SFSMS

SEQ ID NO: 2

VH CDR 2

SISGSSGTTYYADSVKG

SEQ ID NO: 3

VH CDR 3

PFPYFDY

SEQ ID NO: 4

VL CDR 1

RASQSVSSSFLA

SEQ ID NO: 5

VL CDR 2

YASSRAT, and

SEQ ID NO: 6

VL CDR 3

QQTGRIPPT;

wherein the chemotherapy is lomustine;

wherein the antibody molecule comprises the L19 VH domain SEQ ID NO: 7 and the L19 VL domain SEQ ID NO: 9;

wherein the TNFα immunoconjugate comprises TNFα linked to L19 (scFv) as set forth in SEQ ID NO: 10 and

the TNFα immunoconjugate has an amino acid sequence of SEQ ID NO: 13.

12. The method of claim 11 , wherein the immunoconjugate is administered by a route selected from intravenous injection, intratumoural injection, and intrathecal injection.

13. The method of claim 11 , wherein said glioma is selected from a Grade III/IV glioma, a Grade III/IV glioma is at first relapse, an isocitrate dehydrogenase (IDH) wildtype glioma, a newly diagnosed Grade IV glioblastoma, and a Grade IV glioblastoma at first relapse.

14. The method of claim 11 , further comprising administration of radiotherapy.

15. The method of claim 11 , wherein the lomustine is administered at a dose in a range of 50-200 mg/m 2 , or 75-150 mg/m 2 .

16. The method of claim 11 further comprising subsequent administrations of the TNFα immunoconjugate.