Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

Epidemiology and treatment of melanoma in elderly patients

Abstract

The number of melanoma cases in the elderly (>65 years) will rise over the coming decades, making it an important public health problem. Elderly white men are the demographic group who are at highest risk of being diagnosed with melanoma and of dying from this cancer. Among patients with melanoma, older age is recognized as an independent poor prognostic factor, but it remains unclear whether this relationship is due to a change in the biology of the disease with increasing patient age, declining host defenses, or both. Most elderly patients can have surgery to control locoregional disease, but might not be candidates for intensive biologic therapies for advanced melanoma because of comorbidities and inability to tolerate the adverse side effects of these treatments. Early detection remains an important strategy for the management of melanoma. Further research is needed to determine why older melanoma patients have a worse prognosis than their younger counterparts, even when matched for all other clinical and pathological predictors of survival outcomes.

Key Points

  • The number of melanoma cases among the elderly (>65 years) is expected to increase owing to the aging population

  • Older men are at higher risk of developing melanoma, and once diagnosed, are at higher risk of dying from this cancer compared with other demographic groups

  • Older men often present with thicker lesions and a truncal location compared with older women, making self-detection less likely

  • Melanomas in elderly patients often have poor prognostic features compared with younger patients, including ulceration, elevated mitotic rate, and head and neck location

  • Older age is an independent, adverse prognostic factor even after taking all other factors into account

  • Older patients are less likely to receive standard surgery for melanoma, although they usually tolerate these surgeries well

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. He, W., Sengupta, M., Velkoff, V. A. & DeBarros, K. A. 65+ in the United States. US Census Bureau [online], (2005).

    Google Scholar 

  2. Quaglia, A. et al. The cancer survival gap between elderly and middle-aged patients in Europe is widening. Eur. J. Cancer 45, 1006–1018 (2009).

    Article  PubMed  Google Scholar 

  3. Vercelli, M. et al. Relative survival in elderly European cancer patients: evidence for health care inequalities. The EUROCARE Working Group. Crit. Rev. Oncol. Hematol. 35, 161–179 (2000).

    Article  CAS  PubMed  Google Scholar 

  4. Horner, M. J. et al. SEER Cancer Statistics Review, 1975–2006 National Cancer Institute [online], (2009).

    Google Scholar 

  5. Linos, E., Swetter, S. M., Cockburn, M. G., Colditz, G. A. & Clarke, C. A. Increasing burden of melanoma in the United States. J. Invest. Dermatol. 129, 1666–1674 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Geller, A. C. et al. Strategies for improving melanoma education and screening for men age ≥50 years: findings from the American Academy of Dermatological National Skin Cancer Sreening Program. Cancer 95, 1554–1561 (2002).

    Article  PubMed  Google Scholar 

  7. Field, M. J. et al. Extending Medicare coverage for preventive and other services 38–62 (National Academy Press, Washington DC, 2000).

    Google Scholar 

  8. Berg, A. & US Preventive Services Task Force. Screening for skin cancer: Recommendations and rationale. Am. J. Prev. Med. 20 (Suppl. 1), 44–46 (2001).

    Article  Google Scholar 

  9. Geller, A. C., Swetter, S. M., Brooks, K., Demierre, M. F. & Yaroch, A. L. Screening, early detection, and trends for melanoma: current status (2000–2006) and future directions. J. Am. Acad. Dermatol. 57, 555–572 (2007).

    Article  PubMed  Google Scholar 

  10. Jemal, A. et al. Cancer statistics, 2008. CA Cancer J. Clin. 58, 71–96 (2008).

    Article  Google Scholar 

  11. Howe, H. L. et al. Annual report to the nation on the status of cancer (1973 through 1998), featuring cancers with recent increasing trends. J. Natl Cancer Inst. 93, 824–842 (2001).

    Article  CAS  PubMed  Google Scholar 

  12. Jemal, A., Devesa, S. S., Hartge, P. & Tucker, M. A. Recent trends in cutaneous melanoma incidence among whites in the United States. J. Natl Cancer Inst. 93, 678–683 (2001).

    Article  CAS  PubMed  Google Scholar 

  13. Balch, C. M. et al. Prognostic factors analysis of 17,600 melanoma patients: validation of the American Joint Committee on Cancer melanoma staging system. J. Clin. Oncol. 19, 3622–3634 (2001).

    Article  CAS  PubMed  Google Scholar 

  14. Balch, C. M. et al. Final version of the American Joint Committee on Cancer staging system for cutaneous melanoma. J. Clin. Oncol. 19, 3635–3648 (2001).

    Article  CAS  PubMed  Google Scholar 

  15. Schwartz, J. L. et al. Thin primary cutaneous melanomas: associated detection patterns, lesion characteristics, and patient characteristics. Cancer 95, 1562–1568 (2002).

    Article  PubMed  Google Scholar 

  16. Koh, H. K. et al. Who discovers melanoma? Patterns from a population-based survey. J. Am. Acad. Dermatol. 26, 914–919 (1992).

    Article  CAS  PubMed  Google Scholar 

  17. Brady, M. S. et al. Patterns of detection in patients with cutaneous melanoma. Cancer 89, 342–347 (2000).

    Article  CAS  PubMed  Google Scholar 

  18. Epstein, D. S., Lange, J. R., Gruber, S. B., Mofid, M. & Koch, S. E. Is physician detection associated with thinner melanomas? JAMA 2 81, 640–643 (1999).

    Article  Google Scholar 

  19. de Vries, E. et al. Superior survival of females among 10,538 Dutch melanoma patients is independent of Breslow thickness, histologic type and tumor site. Ann. Oncol. 19, 583–589 (2008).

    Article  CAS  PubMed  Google Scholar 

  20. Murray, C. S., Stockton, D. L. & Doherty, V. R. Thick melanoma: the challenge persists. Br. J. Dermatol. 152, 104–109 (2005).

    Article  CAS  PubMed  Google Scholar 

  21. Demierre, M. F., Chung, C., Miller, D. R. & Geller, A. C. Early detection of thick melanomas in the United States: beware of the nodular subtype. Arch. Dermatol. 141, 745–750 (2005).

    PubMed  Google Scholar 

  22. Chao, C. et al. Correlation between prognostic factors and increasing age in melanoma. Ann. Surg. Oncol. 11, 259–264 (2004).

    Article  PubMed  Google Scholar 

  23. Bergenmar, M., Hansson, J. & Brandberg, Y. Detection of nodular and superficial spreading melanoma with tumour thickness ≤2.0 mm—an interview study. Eur. J. Cancer Prev. 11, 49–55 (2002).

    Article  CAS  PubMed  Google Scholar 

  24. Paek, S. C. et al. The impact of factors beyond Breslow depth on predicting sentinel lymph node positivity in melanoma. Cancer 109, 100–108 (2007).

    Article  PubMed  Google Scholar 

  25. Statius Muller, M. G. et al. The sentinel lymph node status is an important factor for predicting clinical outcome in patients with stage I or II cutaneous melanoma. Cancer 91, 2401–2408 (2001).

    Article  CAS  PubMed  Google Scholar 

  26. Gershenwald, J. E. et al. Patterns of recurrence following a negative sentinel lymph node biopsy in 243 patients with stage I or II melanoma. J. Clin. Oncol. 16, 2253–2260 (1998).

    Article  CAS  PubMed  Google Scholar 

  27. Azzola, M. F. et al. Tumor mitotic rate is a more powerful prognostic indicator than ulceration in patients with primary cutaneous melanoma: an analysis of 3661 patients from a single center. Cancer 97, 1488–1498 (2003).

    Article  PubMed  Google Scholar 

  28. Sondak, V. K. et al. Mitotic rate and younger age are predictors of sentinel lymph node positivity: lessons learned from the generation of a probabilistic model. Ann. Surg. Oncol. 11, 247–258 (2004).

    Article  PubMed  Google Scholar 

  29. Attis, M. G. & Vollmer, R. T. Mitotic rate in melanoma: a reexamination. Am. J. Clin. Pathol. 127, 380–384 (2007).

    Article  PubMed  Google Scholar 

  30. Austin, P. F. et al. Age as a prognostic factor in the malignant melanoma population. Ann. Surg. Oncol. 1, 487–494 (1994).

    Article  CAS  PubMed  Google Scholar 

  31. Lasithiotakis, K. et al. Age and gender are significant independent predictors of survival in primary cutaneous melanoma. Cancer 112, 1795–1804 (2008).

    Article  PubMed  Google Scholar 

  32. Balch, C. M. et al. Long-term results of a prospective surgical trial comparing 2 cm vs 4 cm excision margins for 740 patients with 1–4 mm melanomas. Ann. Surg. Oncol. 8, 101–108 (2001).

    CAS  PubMed  Google Scholar 

  33. Cohn-Cedermark, G. et al. Long term results of a randomized study by the Swedish Melanoma Study Group on 2-cm versus 5-cm resection margins for patients with cutaneous melanoma with a tumor thickness of 0.8–20 mm. Cancer 89, 1495–1501 (2000).

    Article  CAS  PubMed  Google Scholar 

  34. Veronesi, U. et al. Thin stage I primary cutaneous malignant melanoma. Comparison of excision with margins of 1 or 3 cm. N. Engl. J. Med. 318, 1159–1162 (1988).

    Article  CAS  PubMed  Google Scholar 

  35. Morton, D. L. et al. Sentinel-node biopsy or nodal observation in melanoma. N. Engl. J. Med. 355, 1307–1317 (2006).

    Article  CAS  PubMed  Google Scholar 

  36. Grange, F. et al. Variations in management of stage I to stage III cutaneous melanoma: a population-based study of clinical practices in France. Arch. Dermatol. 144, 629–636 (2008).

    Article  PubMed  Google Scholar 

  37. Cormier, J. N. et al. Population-based assessment of surgical treatment trends for patients with melanoma in the era of sentinel lymph node biopsy. J. Clin. Oncol. 23, 6054–6062 (2005).

    Article  PubMed  Google Scholar 

  38. Bilimoria, K. Y. et al. Health care system and socioeconomic factors associated with variance in use of sentinel lymph node biopsy for melanoma in the United States. J. Clin. Oncol. 27, 1857–1863 (2009).

    Article  PubMed  Google Scholar 

  39. Bilimoria, K. Y. et al. Complete lymph node dissection for sentinel node-positive melanoma: assessment of practice patterns in the United States. Ann. Surg. Oncol. 15, 1566–1576 (2008).

    Article  PubMed  Google Scholar 

  40. Pan, W. R., Suami, H. & Taylor, G. I. Senile changes in human lymph nodes. Lymphat. Res. Biol. 6, 77–94 (2008).

    Article  PubMed  Google Scholar 

  41. Pawlik, T. M. et al. Predictors and natural history of in-transit melanoma after sentinel lymphadenectomy. Ann. Surg. Oncol. 12, 587–596 (2005).

    Article  PubMed  Google Scholar 

  42. Conway, W. C. et al. Age-related lymphatic dysfunction in melanoma patients. Ann. Surg. Oncol. 16, 1548–1552 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

  43. Wolff, T., Tai, E. & Miller, T. Screening for skin cancer: an update of the evidence for the U.S. Preventive Services Task Force. Ann. Intern. Med. 150, 194–199 (2009).

    Article  PubMed  Google Scholar 

  44. Geller, A. C., Miller, D. R., Swetter, S. M., Demierre, M. F. & Gilchrest, B. A. A call for the development and implementation of a targeted national melanoma screening program. Arch. Dermatol. 142, 504–507 (2006).

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Charles Balch.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tsai, S., Balch, C. & Lange, J. Epidemiology and treatment of melanoma in elderly patients. Nat Rev Clin Oncol 7, 148–152 (2010). https://doi.org/10.1038/nrclinonc.2010.1

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nrclinonc.2010.1

This article is cited by

Search

Quick links

Nature Briefing: Cancer

Sign up for the Nature Briefing: Cancer newsletter — what matters in cancer research, free to your inbox weekly.

Get what matters in cancer research, free to your inbox weekly. Sign up for Nature Briefing: Cancer