The Journal of Urology
Volume 178, Issue 3, Supplement , Pages S25-S29, September 2007

Prostate Specific Antigen Only Androgen Independent Prostate Cancer: Natural History, Challenges in Management and Clinical Trial Design

  • Charles J. Ryan

      Affiliations

    • Department of Medicine and University of California-San Francisco Comprehensive Cancer Center, University of California-San Francisco, San Francisco, California
    • Corresponding Author InformationCorrespondence: Urologic Oncology Program, University of California-San Francisco Comprehensive Cancer Center, 1600 Divisadero St., San Francisco, California 94143 (telephone: 415-353-9279).
  • ,
  • Tomasz M. Beer

      Affiliations

    • Division of Hematology and Medical Oncology, Oregon Health and Science University and Oregon Health and Science University Cancer Institute, Portland, Oregon
    • Financial interest and/or other relationship with Novartis.

published online 18 July 2007.

Purpose

There is no current standard of care for patients with nonmetastatic androgen independent prostate cancer, a condition defined by increasing serum prostate specific antigen despite anorchid testosterone levels and no radiographic evidence of metastases. A consensus panel was convened to review data and propose a strategy for trial design and prioritization.

Materials and Methods

Published literature on the natural history of nonmetastatic androgen independent prostate cancer was reviewed. A panel discussion was held, focusing on reviewing current and past trials, and the development of research priorities for patients in this disease state.

Results

Based on 1 report the natural history of nonmetastatic androgen independent prostate cancer is relatively long but heterogeneous. External validation of these published findings has not been performed. Clinical trial design in this setting is impeded by heterogeneity and lack of knowledge about the natural history, prolonged time to clinical end points, such as the development of metastases or death, and a lack of knowledge about how intermediate end points, eg the development of bone metastases, are related to the long-term outcome, eg survival. In clinical practice a reluctance to use therapies with substantial toxicity as well as a lack of outcome data on such patients leaves a vacuum in which there is no standard of care, although secondary hormonal manipulations are widely used.

Conclusions

Further research is needed to define the natural history of this disease state, educate patients and clinicians about its distinct natural history and develop informative clinical trial designs suited to this patient population.

Key Words: prostate, prostatic neoplasms, prostate-specific antigen, receptors, androgen

Abbreviations and Acronyms: AIPC, androgen independent prostate cancer, AR, androgen receptor, ECOG, Eastern Cooperative Oncology Group, PSA, prostate specific antigen

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PII: S0022-5347(07)00824-5

doi:10.1016/j.juro.2007.03.136

The Journal of Urology
Volume 178, Issue 3, Supplement , Pages S25-S29, September 2007