Failing Zytiga – Some Requirements to Access the MDV-3100 Early Access Trial

Many of us in the United States with advanced prostate cancer who have failed Zytiga are looking to enter the Early Access MDV-3100 Clinical Trial. However, you need to be aware that there are some requirements you will need to meet prior to starting MDV-3100. You will need to wait 30 days after stopping Zytiga [...]

Some Great News for our Fellow European Survivors

Recently, it was announced that there was a submission by Astellas and Medivation to the European Regulatory Agency for Enzalutamide (MDV-3100) for the treatment of men with advanced prostate cancer post-chemotherapy The basis of the submission was the pivotal phase 3 AFFIRM study. The Marketing Authorization Application (MAA) that was made to the European Medicines [...]

Provenge and the Concern about a Rising PSA

There has been an on-going debate on the advanced prostate cancer on-line support group about the issue of the efficacy of Provenge in light of the expectation of a person's increasing PSA number while getting the treatment. For many men with advanced prostate cancer this is a reason they elect to pass on this treatment [...]

Combining MDV-3100 & Provenge – A Wave of the Future?

I have heard some occasional discussion that once (that is if) enzalutamide (MDV-3100) is approved by the FDA for the treatment of men with advanced prostate cancer, it will over shadow Provenge. On the contrary, I believe that the approval of enzalutamide will actually encourage additional use of Provenge resulting in the increasing use of [...]

Emotional & Mental Quality of Life Improved with Early Intervention of Palliative Interventions

Advanced registered nurse practitioners (ARNP) had been integrated into the oncology team at the Mayo Clinic in Jacksonville, Florida with the purpose of discussing palliative care intervention for persons newly diagnosed with metastatic cancer. The team found that this type of intervention improved emotional and mental quality of life (QoL) for those patients who participated [...]

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