Urology
Volume 64, Issue 2 , Pages 317-322, August 2004

Measurement of insulin-like growth factor axis does not enhance specificity of PSA-based prostate cancer screening

  • Steven E Oliver

      Affiliations

    • Department of Health Sciences, University of York and Hull York Medical School, York, United Kingdom
    • Corresponding Author InformationReprint requests: Steven E. Oliver, Ph.D., M.R.C.P., M.F.P.H.M., Department of Health Sciences, University of York and Hull York Medical School, Seebohm Rowntree Building, Heslington, York YO10 5DD, United Kingdom
  • ,
  • Jeff Holly

      Affiliations

    • Division of Surgery, University of Bristol, Bristol Royal Infirmary, Bristol, United Kingdom
  • ,
  • Tim J Peters

      Affiliations

    • Division of Primary Health Care, University of Bristol, Bristol, United Kingdom
  • ,
  • Jenny Donovan

      Affiliations

    • Department of Social Medicine, University of Bristol, Bristol, United Kingdom
  • ,
  • Raj Persad

      Affiliations

    • Division of Surgery, University of Bristol, Bristol Royal Infirmary, Bristol, United Kingdom
  • ,
  • David Gillatt

      Affiliations

    • Bristol Urological Institute, Southmead Hospital, Bristol, United Kingdom
  • ,
  • Anya Pearce

      Affiliations

    • Division of Surgery, University of Bristol, Bristol Royal Infirmary, Bristol, United Kingdom
  • ,
  • Freddie C Hamdy

      Affiliations

    • Academic Urology Unit, Division of Clinical Sciences, University of Sheffield, Sheffield, United Kingdom
  • ,
  • David E Neal

      Affiliations

    • Oncology Centre, Addenbrooke's Hospital, Cambridge, United Kingdom
  • ,
  • David Gunnell

      Affiliations

    • Department of Social Medicine, University of Bristol, Bristol, United Kingdom

Received 17 June 2003; accepted 9 March 2004.

Abstract 

Objectives

To examine whether measurement of insulin-like growth factor (IGF)-I, IGF-II, IGF binding protein (IGFBP)-2 or IGFBP-3, alone or in combination, enhanced the specificity of prostate cancer detection among men with a prostate-specific antigen (PSA) level of 3 ng/mL or greater beyond that achieved by the free/total PSA index.

Methods

Cross-sectional analysis was performed on blood samples taken from 597 asymptomatic men (79% of those biopsied) participating in a community case-finding exercise. All men had a total PSA level of 3 ng/mL or greater and had undergone prostate biopsy. Assays of IGF-I, IGF-II, IGFBP-2, IGFBP-3, and free and total PSA were performed. The predictive performance of a range of measures was assessed using receiver operating characteristic analyses and compared with the free/total PSA index, for all biopsies and for men with a PSA level of 3 to 10 ng/mL. The overall test performance was summarized using the area under the receiver operating characteristic curve (AUC).

Results

Of the 597 men, 185 (31.0%) had prostate cancer identified at biopsy. When all biopsies were included, the performance of the free/total PSA index (AUC 0.73) was significantly greater than for IGF-I (AUC 0.59; P <0.0001), IGF-I/PSA ratio (AUC 0.65; P = 0.002), IGF-I + IGFBP-3 (AUC 0.59; P <0.0001), IGF-II (AUC 0.66; P = 0.002), and IGF-II + IGFBP-3 (AUC 0.67; P = 0.05). The combined measurement of free/total PSA, IGF-II, and IGFBP-3 resulted in a slight improvement in performance (AUC 0.76; P = 0.01). The results were similar when the analyses were restricted to men with an initial PSA level of 3 to 10 ng/mL.

Conclusions

We found no evidence that measurement of the IGF axis enhances the specificity of prostate cancer detection in clinical practice beyond that achievable using the free/total PSA index.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 This research was funded by NHS South and West R&D; and the ProtecT treatment trial was funded by the NHS Health Technology Assessment Programme.

PII: S0090-4295(04)00335-8

doi:10.1016/j.urology.2004.03.018

Urology
Volume 64, Issue 2 , Pages 317-322, August 2004