Co-administration of cG250 and IL-2 or IFN-α for treating cancer such as renal cell carcinomas
View Patent ↗A method for enhancing the therapeutic effect of cytokine treatment is disclosed. More specifically the present invention relates to a method for administering to a tumor patient a therapeutic dose of cytokine in combination with antibodies directed against the tumor associated antigen carbonic anhydrase IX (CAIX/G250/MN). The improved treatment method is characterized in a significantly reduced cytokine-related toxicity combined with potentiated effectiveness of anti-G250 antibody alone, resulting in a positive therapeutic response with respect to that observed with single anti-tumor agents alone.
1. A method for the treatment of renal cell cancer comprising co-administering an anti-tumor antibody directed against the MN antigen, wherein said antitumor antibody is a chimeric or humanized G250 antibody or an antigen binding fragment thereof and a cytokine to a subject in need thereof, wherein the cytokine is IFN-α and is administered continuously or repeatedly in a low-dose form, wherein the low-dose cytokine comprises a dose which is pharmaceutically effective in the absence of NIC CTC toxicity grade 3 or higher, and wherein said G250 antibody or fragment thereof and said IFN-α are the only active ingredients which are administered.
2. A method for the treatment of renal cell cancer comprising co-administering an anti-tumor antibody G250 directed against the MN antigen and cytokine to a subject in need thereof, wherein the cytokine consists of interferon-α and the method comprises:
(a) a first treatment stage comprising administering a low-dose interferon-α, and
(b) a second treatment stage comprising co-administering the anti-tumor antibody G250 and a low-dose interferon-α as the only active ingredients, and wherein the low-dose interferon-α comprises a dose which is pharmaceutically effective in the absence of NIC CTC toxicity grade 3 or higher.
3. The method according to claim 1 comprising a daily administration of a low-dose cytokine.
4. The method of claim 1 , wherein the dose of IFN-α is in the range of from 1-10 MIU three times a week.
5. The method of claim 1 wherein the cytokine is administered in a constant dose during the treatment.
6. The method of claim 1 wherein the IFN-α is administered subcutaneously.
7. The method of claim 1 wherein the antitumor antibody G250 is administered in intervals of from 5-20 days.
8. The method of claim 2 wherein the first treatment stage comprises 5-20 days.
9. The method of claim 2 wherein the second treatment stage comprises 50-200 days.
10. A method for the treatment of renal cell cancer comprising co-administering an anti-tumor antibody G250 or an antigen binding fragment thereof and a cytokine IFN-α as the only active ingredients to a subject in need thereof, wherein the cytokine is administered continuously or repeatedly in a low-dose form, wherein the low-dose cytokine comprises a dose which is pharmaceutically effective in the absence of NIC CTC toxicity grade 3 or higher.
11. A method for the treatment of renal cell cancer consisting essentially of co-administering an anti-tumor antibody directed against the MN antigen, wherein said antitumor antibody is a chimeric or humanized G250 antibody or an antigen binding fragment thereof and a cytokine to a subject in need thereof, wherein the cytokine is IFN-α and is administered continuously or repeatedly in a low-dose form, wherein the low-dose cytokine comprises a dose which is pharmaceutically effective in the absence of NIC CTC toxicity grade 3 or higher and wherein said IFN-α is the only cytokine which is administered.