A Phase 2 Randomized Study of Abiraterone Acetate, Enzalutamide or Apalutamide as First Line Therapy in Veterans With Castrate-sensitive Prostate Cancer
Summary
The investigators have used national VHA data to demonstrate real-world efficacy of abiraterone and enzalutamide in Veterans with mCRPC. In the real-world that is the VHA, the investigators have successfully estimated g values that accurately predict OS and the use of this metric in other settings should now be explored. In the egalitarian system that is the VHA the treatment of prostate cancer is excellent and uniform across the US. The choices made are clearly personalized, given not all men received all therapies and that younger Veterans were treated more aggressively. But with survivals that rival those in registration trials that enroll optimally fit individuals usually not encumbered by the co-morbidities that afflict many Veterans, the outcomes are testimony to the fact that for this common malady of older Veterans with whom VA physicians have broad experience the care administered is unsurpassed. Importantly this care at least as regards Veterans with mCRPC demonstrates that given equal access to health care, all men with prostate cancer fare comparably well. As our sophistication in categorizing cancers molecularly has increased this study will look to better examine any emerging differences across study participants.
Arms & interventions
- DrugAbiraterone acetate
YONSA® (fine particle formulation abiraterone acetate), YONSA® 500 mg (four 125 mg tablets) or 625 mg (five 125 mg tablets) administered orally once daily in combination with methylprednisolone 4 mg administered orally twice daily + physician's choice GnRH agonist/antagonist \[unless the Veteran has had prior bilateral orchiectomy\]. Note that in the first four months the YONSA® dose should not exceed 500 mg administered orally once daily. ZYTIGA® (abiraterone acetate) or generic ZYTIGA 1000 mg (four 250 mg uncoated tablets or two 500 mg film-coasted tablets) administered orally once daily in combination with prednisone 5 mg administered orally once daily + physician's choice GnRH agonist/antagonist \[unless the Veteran has had prior bilateral orchiectomy\].
- DrugApalutamide
Apalutamide (ERLEADA®), 240 mg (four 60 mg tablets) administered orally once daily + physician's choice GnRH agonist/antagonist \[unless the Veteran has had prior bilateral orchiectomy\].
- DrugEnzalutamide
Enzalutamide (XTANDI®), 160 mg (four 40 mg capsules) administered orally once daily + physician's choice GnRH agonist/antagonist \[unless the Veteran has had prior bilateral orchiectomy\].
Outcome measures
Primary
Tumor growth rate (g)
Tumor growth rate (g)
Time frame: 2 years
Testosterone levels
Testosterone levels to assess testosterone suppression with androgen deprivation therapy (ADT).
Time frame: 2 years
Secondary
PSA Response
Time frame: 2 years
Eligibility criteria
Study locations (12)
VA Greater Los Angeles Healthcare System
Los Angeles, California, 90073
James A. Haley Veterans Administration Hospital
Tampa, Florida, 33612
VA Ann Arbor Healthcare System
Ann Arbor, Michigan, 48105
VA St. Louis Health Care System
St Louis, Missouri, 63106
VA New York Harbor Healthcare System
New York, New York, 10010
James J. Peters VA Medical Center
The Bronx, New York, 10468
VA Hudson Valley Health Care System
Wappingers Falls, New York, 12590
W.G. Bill Hefner Medical Center
Salisbury, North Carolina, 28144
VA Portland Health Care System
Portland, Oregon, 97239
Corporal Michael J. Crescenz VA Medical Center
Philadelphia, Pennsylvania, 19104
Michael E. DeBakey VA Medical Center
Houston, Texas, 77030
VA Puget Sound Health Care System
Seattle, Washington, 98108