Methods for cancer treatment
US-10549082-B2 · Feb 4, 2020 · US
US11547842B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11547842-B2 |
| Application number | US-201916716102-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 16, 2019 |
| Priority date | Apr 17, 2013 |
| Publication date | Jan 10, 2023 |
| Grant date | Jan 10, 2023 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Residual, refractory or relapsed cancer is treated by immunostimulation in the presence of allogeneic immune effector cells, optimally in combination with radiation therapy. The methods of the disclosure induce a systemic allogeneic anti-tumor immune response that results in tumor regression in untreated sites of disease, i.e. non-injected, non-irradiated, etc.
Opening claim text (preview).
What is claimed: 1. A method of treating a cancer in a subject, the method comprising intratumorally administering into a tumor in the subject that has undergone an allogenic hematopoietic stem cell transplantation an immunostimulant while concurrently providing local field irradiation of the tumor in the subject's body, wherein a combination of the immunostimulant and the local field irradiation induces allogeneic immune cells to generate an anti-tumor response to HLA alloantigens expressed by the tumor, causing a systemic allogeneic anti-tumor T-cell immune response that results in tumor regression in a second, untreated site of disease in the subject's body. 2. The method of claim 1 , wherein said allogeneic anti-tumor T cell immune response further comprises at least about 5% circulating allogeneic type CD3+ T cells. 3. The method of claim 1 , wherein said subject has at least about 5% allogeneic type leukocytes. 4. The method of claim 1 , wherein said irradiation is an irradiation at a tumor nodule. 5. The method of claim 1 , wherein said irradiation is selected from the group consisting of ionizing radiation, thermal therapy, ultrasound, irreversible electroporation (IRE), oxidative stress, radiofrequency ablation and combinations thereof. 6. The method of claim 1 , wherein said immunostimulant is an oligodeoxynucleotide (ODN), said ODN further comprises a CpG that binds to a Toll-Like Receptor (TLR) 9 so as to activate dendritic cells and B-cells. 7. The method of claim 1 , wherein said cancer is a solid tumor or a lymphoma. 8. The method of claim 7 , wherein said cancer is a lymphoma, said lymphoma is selected from the group consisting of a Non-Hodgkin's lymphoma, a Hodgkin's lymphoma, a cutaneous T-cell lymphoma and a mycosis fungoides. 9. The method of claim 1 , wherein said cancer is a renal cell carcinoma. 10. The method of claim 1 , wherein said cancer is selected from the group consisting of a residual cancer, a relapsed cancer and a refractory cancer. 11. The method of claim 1 , wherein said second, untreated site of disease further comprises a tumor that has not been injected with said immunostimulant.
by means of electrically-heated probes · CPC title
X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy (A61N5/01 takes precedence) · CPC title
Double-stranded nucleic acids or oligonucleotides · CPC title
Ultrasound therapy (lithotripsy A61B17/22, A61B17/225; massage using supersonic vibration A61H23/00 {; using ultrasound for introducing media into the body A61M37/0092}) · CPC title
Murine · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.