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Microvessel density as a prognostic factor in penile squamous cell carcinoma

  • Amr Al-Najar, M.D.

      Affiliations

    • Department of Urology and Pediatric Urology, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany
    • Corresponding Author InformationCorresponding author. Tel.: +49-431-597-4411; fax: +49-431-597-1957
    • These authors contributed equally to this work.
  • ,
  • Sakhr Al-Sanabani, M.D.

      Affiliations

    • Department of Pathology, Neuköln Clinic, Vivantes, Berlin, Germany
    • These authors contributed equally to this work.
  • ,
  • Joanna Beate Korda, M.D.

      Affiliations

    • Department of Urology, University Hospital Cologne, Cologne, Germany
  • ,
  • Axel Hegele, M.D.

      Affiliations

    • University Hospital Giessen and Marburg GmbH, Marburg, Germany
  • ,
  • Christian Bolenz, M.D.

      Affiliations

    • University Hospital Mannheim, Mannheim, Germany
  • ,
  • Hermann Herbst, M.D.

      Affiliations

    • Department of Pathology, Neuköln Clinic, Vivantes, Berlin, Germany
  • ,
  • Klaus-Peter Jünemann, M.D.

      Affiliations

    • Department of Urology and Pediatric Urology, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany
  • ,
  • Carsten Maik Naumann, M.D.

      Affiliations

    • Department of Urology and Pediatric Urology, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany

Received 12 February 2010; received in revised form 24 March 2010; accepted 26 March 2010. published online 21 June 2010.
Corrected Proof

Abstract 

Objective

To examine the potential effect of tumor-induced angiogenesis in squamous cell carcinoma of the penis as a possible prognostic factor.

Patients and methods

Immunohistochemistry was preformed to detect microvessels in tumor samples of 64 patients with squamous cell carcinoma of the penis. We used a monoclonal mouse antibody directed against CD34 antigen. Only 61 (30 with and 31 without metastasis) patients had good staining properties and were included. After immunostaining, the entire tumor section was scanned microscopically at low power (×40) to identify hot spots within the tumor and at its periphery. Individual tumor microvessels were then counted under high power (×200) to obtain a vessel count in a defined area, and the mean of the 3 highest microvessel counts was taken as the microvessel density (MVD). Microvessel counting was performed using a computer-aided image analysis system. The nodal status was based on histopathologic examination or an uneventful follow-up ≥2 years.

Results

The 5-year overall survival (OAS) was 75% and 30 % for those with high and low peritumoral MVD, respectively (log rank P = 0.01). No difference was noticed within the tumor with regard to high (5-year OAS of 65.03%) and low (5-year OAS of 60.56%) intratumoral MVD (log rank P = 0.99). The mean intratumoral MVD was 32.35 (3.16), 37.94 (3.35), and 62.66 (5.47) in T1, T2, and T3 respectively (ANOVA P = 0.0006), with increasing tendency. The mean peritumoral MVD was 55.91 (5.60), 56.8 (4.00), and 78.86 (8.71), respectively (P = 0.06). No correlation between MVD lymph node status and tumor grade was seen (P > 0.05).

Conclusion

In our group of patients, a high peritumoral MVD was associated with a better 5-year OAS. However, for a reliable and reproducible assessment of tumor angiogenesis in penile squamous cell carcinoma, validation procedures and quality control protocols are mandatory.

Keywords: Penile cancer, Microvessel density, Angiogenesis

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PII: S1078-1439(10)00072-4

doi:10.1016/j.urolonc.2010.03.016

« BackUrologic Oncology: Seminars and Original Investigations