The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jul. 16, 2024

Filed:

Mar. 28, 2022
Applicant:

Memorial Sloan-kettering Cancer Center, New York, NY (US);

Inventors:

Richard Kolesnick, New York, NY (US);

Adriana Haimovitz-Friedman, New York, NY (US);

Evis Sala, New York, NY (US);

Zvi Fuks, New York, NY (US);

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 31/4439 (2006.01); A61K 31/337 (2006.01); A61K 31/404 (2006.01); A61K 31/7048 (2006.01); A61K 31/7068 (2006.01); A61K 45/06 (2006.01); A61P 35/00 (2006.01); C12Q 1/48 (2006.01); G01N 33/574 (2006.01);
U.S. Cl.
CPC ...
A61K 31/4439 (2013.01); A61K 31/337 (2013.01); A61K 31/404 (2013.01); A61K 31/7048 (2013.01); A61K 31/7068 (2013.01); A61K 45/06 (2013.01); A61P 35/00 (2018.01); C12Q 1/485 (2013.01); G01N 33/57488 (2013.01); G01N 2800/52 (2013.01);
Abstract

Disclosed is a method for enhancing tumor response to chemotherapy, the method comprising administering a short-acting anti-angiogenic agent (AAA) capable of activating ASMase to a subject afflicted with a solid tumor, and thereby creating a time interval of increased susceptibility of said tumor to one or more chemotherapeutic agents, followed by administration of at least one chemotherapeutic agent within the interval. The interval can be defined in terms of a short-duration activation of ASMase signaling by the AAA. Disclosed are also methods for predicting the tumor response in a patient afflicted with a solid tumor to a chemotherapeutic agent, using as an indicator of the response ASMase level or activity (or ceramide level) in the patient following the administration of the chemotherapeutic agent to the patient, or dynamic IVIM based DW-MRI to measure perfusion alterations following administration of the chemotherapeutic agent.


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