Breast Cancer Drugs are More Effective than Standard Therapy for Prostate Cancer! An important clinical trial reports that a drug already approved for the treatment of breast and ovarian cancer is more effective than targeted hormone therapy in controlling cancer in some patients with advanced prostate cancer. Olapani is a drug without the side effects of chemotherapy, which can treat the Achilles' heel of prostate cancer, that is, a weak ability to repair damaged DNA. Now, it is about to be approved as the first gene-targeted therapy for prostate cancer. This precise drug, called a PARP inhibitor, specifically targets cancer cells with defective DNA repair genes and prevents prostate cancer growth more effectively than the modern targeted hormone therapies abiraterone and enzalutamide. The final results of this far-reaching trial, published in The New England Journal of Medicine today, herald the landmark approval of prostate cancer drugs in the United States and Europe this year. This study was funded by AstraZeneca. A team of researchers from the London Cancer Institute and the Royal Marsden NHS Foundation, together with colleagues from around the world, including Northwestern University in Chicago, USA, studied 387 patients with advanced prostate cancer whose 15 DNA repair genes were altered. The researchers found that using olaparib in men with defects in this group of DNA repair genes significantly delayed the progression of the disease. Prostate cancer patients with BRCA1, BRCA2, or ATM gene defects benefit most from treatment with olaparib, and they have a progression-free survival of 7.4 months compared with 3.6 months for patients taking enzalutamide and abiraterone. Men with 12 additional preselected alterations in DNA repair genes also benefited from olaparib. Overall, men with defects in any of the 15 DNA repair genes had an average of 5.8 months before their cancer worsened after using oraparib, compared with 3.5 months for men using targeted hormone therapy. Abiraterone, discovered by the Cancer Institute (ICR) and developed by ICR and Royal Marsden, has changed the treatment of advanced prostate cancer. The investigators are excited about the prospect of olaparib because ICR has discovered a genetically targeted approach and olaparib may be more effective than abiraterone in men with DNA repair mutations. Men with BRCA1, BRCA2, or ATM gene defects had an overall survival of 19 months after treatment with olaparib, compared with 15 months after treatment with enzalutamide and abiraterone—although 80% of patients switched to olaparib after cancer progression and