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US 12,523,657 B2Granted
DNA repair blood test for predicting response of lung cancer patients to immunotherapy
AssigneeYeda Research and Development Co. Ltd.
InventorsZvi Livneh, Tamar Paz-Elizur
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Abstract
A method of selecting a treatment for a subject having cancer is disclosed. The method comprises: (a) determining a level of catalytic activity of at least one DNA repair enzyme in a biological sample of the subject; and (b) selecting an immune checkpoint regulator as a treatment for a subject having a statistically significant different level of catalytic activity of the DNA repair enzyme as compared to the catalytic activity of the DNA repair enzyme in a biological sample of a healthy subject.
Claims22
A method of treating a subject having cancer, the method comprising:
- (a) determining a level of catalytic activity of the DNA repair enzymes N-methylpurine DNA glycosylase (MPG), apurinic/apyrimidinic endonuclease 1 (APE1), 8-oxoguanine DNA glycosylase 1 (OGG1) in a biological sample of the subject;
- and
- (b) [i] administering to a subject having a statistically significant different level of catalytic activity of said DNA repair enzymes as compared to the catalytic activity of said DNA repair enzyme in a biological sample of a healthy subject, a therapeutically effective amount of an immune checkpoint regulator;
- or
- [ii] administering to a subject having a non-statistically significant different level of catalytic activity of said DNA repair enzymes as compared to the catalytic activity of said DNA repair enzyme in a biological sample of a healthy subject, a therapeutically effective amount of an anti-cancer agent other than said immune checkpoint regulator, thereby treating the cancer;
- wherein determining said MPG catalytic activity is effected using a double stranded oligonucleotide substrate having a hypoxanthine lesion (Hx),
- wherein determining said MPG catalytic activity is effected using an oligonucleotide substrate having an N6-ethenoadenine lesion (eA),
- wherein determining said APE1 catalytic activity is effected using an oligonucleotide substrate having a furanyl abasic site lesion (AP) or
- wherein determining said OGG1 catalytic activity is effected using an oligonucleotide substrate having an 8-oxoguanine lesion.
6 more elements
Dependencies are inferred from the claim text.