| CPC A61K 31/502 (2013.01) [A61K 31/498 (2013.01); A61P 35/00 (2018.01); A61P 35/04 (2018.01)] | 18 Claims |
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1. A method for delaying pain progression in a subject receiving treatment for prostate cancer, the method comprising:
administering to the subject a therapeutically effective amount of 4-[(3-{[4-(cyclopropane-carbonyl) piperazine-1-yl]carbonyl}-4-fluorophenyl) methyl]-2H-phthalazin-1-one (olaparib), or a hydrate, solvate, or prodrug thereof, wherein the therapeutically effective amount of olaparib is about 600 mg daily; then
identifying the subject as having pain progression as evaluated by a pain questionnaire or an opioid use log and administering to the subject a therapeutically effective amount of an opiate;
wherein the time to pain progression in the subject is delayed by at least 10 months as compared to the time to pain progression in a subject receiving the standard of care treatment; and
wherein the administration of the opiate to the subject is delayed by at least 10 months as compared to administration of an opiate in a subject receiving the standard of care treatment.
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