The Journal of Urology
Volume 177, Issue 5 , Pages 1777-1781, May 2007

Adjuvant Weekly Docetaxel for Patients With High Risk Prostate Cancer After Radical Prostatectomy: A Multi-Institutional Pilot Study

  • Adam S. Kibel

      Affiliations

    • Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri
    • Corresponding Author InformationCorrespondence: Division of Urologic Surgery, Washington University School of Medicine, 4960 Children’s Pl., Box 8242, St. Louis, Missouri 63105 (telephone: 314-362-8295).
  • ,
  • Eli Rosenbaum

      Affiliations

    • Sidney Kimmel Comprehensive Care Center, Johns Hopkins Medical Institutions, Baltimore, Maryland
  • ,
  • Michael W. Kattan

      Affiliations

    • Cleveland Clinic, Cleveland, Ohio
  • ,
  • Joel Picus

      Affiliations

    • Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri
  • ,
  • Robert Dreicer

      Affiliations

    • Cleveland Clinic, Cleveland, Ohio
  • ,
  • Eric A. Klein

      Affiliations

    • Cleveland Clinic, Cleveland, Ohio
  • ,
  • Gurkamal S. Chatta

      Affiliations

    • University of Pittsburgh, Pittsburgh, Pennsylvania
  • ,
  • Joel B. Nelson

      Affiliations

    • University of Pittsburgh, Pittsburgh, Pennsylvania
  • ,
  • Robert S. DiPaola

      Affiliations

    • Robert Wood Johnson Medical School, Piscataway, New Jersey
  • ,
  • Bruce J. Roth

      Affiliations

    • Vanderbilt-Ingram Cancer Center, Nashville, Tennessee
  • ,
  • Michael S. Cookson

      Affiliations

    • Vanderbilt-Ingram Cancer Center, Nashville, Tennessee
  • ,
  • George Wilding

      Affiliations

    • University of Wisconsin Paul P. Carbone Comprehensive Cancer Center, Madison, Wisconsin
  • ,
  • David F. Jarrard

      Affiliations

    • University of Wisconsin Paul P. Carbone Comprehensive Cancer Center, Madison, Wisconsin
  • ,
  • Tomasz M. Beer

      Affiliations

    • Oregon Health and Science University, Portland, Oregon
  • ,
  • Christopher W. Ryan

      Affiliations

    • Oregon Health and Science University, Portland, Oregon
  • ,
  • Daniel P. Petrylak

      Affiliations

    • Columbia-Presbyterian Medical Center, New York, New York
  • ,
  • Mitchell C. Benson

      Affiliations

    • Columbia-Presbyterian Medical Center, New York, New York
  • ,
  • Alan W. Partin

      Affiliations

    • Sidney Kimmel Comprehensive Care Center, Johns Hopkins Medical Institutions, Baltimore, Maryland
  • ,
  • Elizabeth Garrett-Mayer

      Affiliations

    • Sidney Kimmel Comprehensive Care Center, Johns Hopkins Medical Institutions, Baltimore, Maryland
  • ,
  • Mario A. Eisenberger

      Affiliations

    • Sidney Kimmel Comprehensive Care Center, Johns Hopkins Medical Institutions, Baltimore, Maryland

Received 23 October 2006

Purpose

Patients with adverse pathological features are at high risk for recurrence following radical prostatectomy. To improve outcomes in this population we performed a phase II study of adjuvant docetaxel in these high risk patients.

Materials and Methods

Patients with nonmetastatic radical prostatectomy at greater than 50% risk for recurrence by 3 years were eligible. Pathological findings were centrally reviewed and risk assessment was based on a validated multivariate Cox proportional hazards model. Treatment consisted of 6 cycles of 35 mg/m2 docetaxel weekly given 4 to 12 weeks following surgery. Progression was defined as a prostate specific antigen of 0.4 ng/ml or greater, radiological/pathological evidence of recurrent disease or death from any cause. To screen for the potential benefit of adjuvant weekly docetaxel we used nomogram predicted progression-free survival as a historical control.

Results

A total of 77 patients were registered between April 2002 and January 2004. Two patients had grade IV hyperglycemia and 20 had grade III toxicity. At a median followup of 29.2 months (range 1.6 to 39.2) 46 of 76 evaluable cases (60.5%) progressed. Observed median progression-free survival was 15.7 months (95% CI 12.8–25.1). Predicted median progression-free survival in a matched population was 10 months. Seven patients died, including 4 of prostate cancer, 1 with intra-abdominal bleeding during treatment and 2 of pneumonia and sudden cardiac death, respectively, following treatment.

Conclusions

Adjuvant docetaxel for prostate cancer is feasible with significant reversible but acceptable toxicity. The actual median progression-free survival of 15.7 months was longer than the nomogram predicted rate for this patient population. Adjuvant docetaxel treatment should be further evaluated in phase III trials in patients with high risk prostate cancer.

Key Words: prostate, prostatic neoplasms, drug therapy, prostatectomy, mortality

Abbreviations and Acronyms: CT, computerized tomography, PFS, progression-free survival, PSA, prostate specific antigen, RP, radical prostatectomy, Rw′, weighted risk of recurrence, SWOG, Southwest Oncology Group

 

 Study received institutional review board approval.

 Supported by Sanofi-Aventis.

PII: S0022-5347(07)00079-1

doi:10.1016/j.juro.2007.01.028

The Journal of Urology
Volume 177, Issue 5 , Pages 1777-1781, May 2007