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Enzalutamide Maintains HRQoL in High-Risk Recurrent nmCSPC - Renal and Urology News

Multiple surveys of patient-reported outcomes from the phase 3 EMBARK trial revealed no meaningful differences in pain progression or urinary symptoms and bowel symptoms or function over 205 weeks of follow-up. Enzalutamide does not worsen health-related quality of life compared with androgen deprivation therapy in patients with high-risk biochemically recurrence nmCSPC. ....

United States , Stephenj Freedland , Los Angeles , Society Of Urologic Oncology , Research In Cancer , European Organization For Research , Samuel Oschin Comprehensive Cancer Institute , Urologic Oncology , Integrated Research , Samuel Oschin Comprehensive Cancer , Brief Pain Inventory Short Form , Functional Assessment , Cancer Therapy Prostate , European Qol , European Organization , Cancer Qol Questionnaire Prostate ,

FDA Approves Xtandi for High-Risk Prostate Cancer

The Food and Drug Administration approved Xtandi for non-metastatic castration-sensitive prostate cancer at high risk for biochemical recurrence. ....

Courtney Bugler , European Society Of Medical Oncology , Drug Administration , Carolina Urologic Research Center , Neal Shore , Genesiscare United States , New England Journal , Medical Oncology , Brief Pain Inventory Short Form , Functional Assessment , Cancer Therapy Prostate , Prostate Cancer ,

Enzalutamide Improves Metastasis-Free Survival in Biochemically Recurrent PCa

Treatment intensification with the androgen receptor inhibitor enzalutamide shows benefit in patients with biochemically recurrent prostate cancer. Data show enzalutamide treatments are safe and effective compared with ADT alone in patients with high-risk biochemically recurrent prostate cancer. ....

Stephenj Freedland , Astellas Pharma , Los Angeles , Drug Administration , New England Journal , Law Families Chair , Prostate Cancer , Functional Assessment , Cancer Therapy Prostate ,

AstraZeneca and MSD's Lynparza approved in the EU for prostate cancer

AstraZeneca and MSD's Lynparza approved in the EU for prostate cancer ....

Dave Fredrickson , Noel Clarke , Manchester Christie Salford , Eliav Barr , Manchester University , Research Laboratories , European Union , European Commission , Head Of Global Clinical Development , Medicinal Products , Human Use , Neurological Surgeon , Urological Oncology , Salford Royal Hospitals , Executive Vice President , Oncology Business Unit , Senior Vice President , Global Clinical Development , Chief Medical Officer , Functional Assessment , Cancer Therapy Prostate , New Drug Application , Priority Review , Prescription Drug User Fee Act ,

AstraZeneca (AZN) Announces Lynparza with Abiraterone Approved in EU for mCRPC

AstraZeneca (AZN) Announces Lynparza with Abiraterone Approved in EU for mCRPC
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Dave Fredrickson , Noel Clarke , Manchester Christie Salford , Eliav Barr , Manchester University , Research Laboratories , European Union , European Commission , Head Of Global Clinical Development , Medicinal Products , Human Use , Neurological Surgeon , Urological Oncology , Salford Royal Hospitals , Executive Vice President , Oncology Business Unit , Senior Vice President , Global Clinical Development , Chief Medical Officer , Functional Assessment , Cancer Therapy Prostate , New Drug Application , Priority Review , Prescription Drug User Fee Act , Collaboration Revenue ,