Annals of Surgical Oncology

, Volume 5, Issue 3, pp 253–260

Molecular oncogene markers and their significance in cutaneous malignant melanoma

  • Manoussos M. Konstadoulakis
  • Michael Vezeridis
  • Emi Hatziyianni
  • Constantine P. Karakousis
  • Bernard Cole
  • Kirby I. Bland
  • Harold J. Wanebo
Original Articles

DOI: 10.1007/BF02303782

Cite this article as:
Konstadoulakis, M.M., Vezeridis, M., Hatziyianni, E. et al. Annals of Surgical Oncology (1998) 5: 253. doi:10.1007/BF02303782

Abstract

Background: Oncogenes and other molecular tumor markers that predict tumor aggressiveness may allow individualization and optimization of surgical therapy of intermediate-thickness malignant melanoma. We examined the expression of selected markers, including the HLA-DR antigen, the heat shock protein-70 (HSP-70), and the c-myc oncogene in primary melanoma and regional nodes and related these findings to metastatic potential and survival.

Methods: Forty patients with primary melanoma (1.5–4.0 mm) were studied, all of whom had prophylactic lymph node dissection and were followed for 18 months to 7 years. The primary tissue and nodes were examined using immunohistochemical techniques for the presence of HLA-DR antigen and HSP-70 protein and the expression of the c-myc oncogene.

Results: Of 40 patients, there were 23 with lesions 1 to 2.9 mm thick and 17 with lesions 3 to 4 mm thick. Nodal metastases were present in 25 of the 40 patients who had elective node dissection. HLA-DR antibody stained the primary tumor in 10 patients (25%), but there was no correlation with survival in this group. HLA-DR antibody stained the stroma and cellular infiltrates surrounding the primary tumor in 28 of 40 patients; in this group there was a correlation of HLA-DR staining of the peritumoral stroma with improved survival overall. HLA-DR staining of the peritumoral stroma also influenced survival when patients were stratified by tumor thickness groups 1 to 2.9 mm and 3 to 4 mm and presence of nodal metastases. HSP-70 was demonstrated in the primary tumor in 25% of patients, who were also shown to have significantly improved survival when compared with those whose primary tumor did not stain with HSP-70. C-myc was expressed in the primary tumor in 25%, but showed no correlation with survival. None of these proteins correlated with or predicted the presence of nodal metastases.

Conclusion: We conclude that the use of specific molecular-oncogene markers in intermediate-thickness primary melanoma may identify patients at high risk for conventional treatment failure and reduced survival who may profit from more aggressive surgery, adjuvant therapy, or both.

Key words

Malignant melanomaHSP-70HLA-DR antigenc-myc oncogenePrognostic factorsNode dissection

Copyright information

© The Society of Surgical Oncology, Inc. 1998

Authors and Affiliations

  • Manoussos M. Konstadoulakis
    • 2
  • Michael Vezeridis
    • 1
  • Emi Hatziyianni
    • 3
  • Constantine P. Karakousis
    • 3
  • Bernard Cole
    • 4
  • Kirby I. Bland
    • 2
  • Harold J. Wanebo
    • 2
  1. 1.From the Division of Surgical OncologyBrown University School of Medicine, Center for Statistical Science, Brown UniversityProvidence
  2. 2.Department of SurgeryBrown University School of Medicine, Center for Statistical Science, Brown UniversityProvidence
  3. 3.the Department of Surgical OncologyRoswell Park Cancer InstituteBuffalo
  4. 4.Dept. of SurgeryRoger Williams Medical CenterProvidence