Cutaneous melanoma and intervention strategies to reduce tumor-related mortality: what we know, what we don't know, and what we think we know that isn't so
- PMID: 16405570
- DOI: 10.1111/j.1529-8019.2005.00056.x
Cutaneous melanoma and intervention strategies to reduce tumor-related mortality: what we know, what we don't know, and what we think we know that isn't so
Abstract
The care of patients who have cutaneous melanoma (CM) has undergone a dramatic change during the past five decades. In an increasing majority of cases, CM is being discovered in a premetastatic phase of tumor progression. Most patients are being treated in the ambulatory setting with a minimum of inconvenience and economic cost, and modest re-excision margins have largely replaced the mutilating surgical exonerations that were once standard only four decades ago. Histopathologic assessment of the primary tumor is the most widely used staging procedure to determine who is most likely to develop metastatic disease. For patients who develop distant metastases, there is no therapy currently available, based on large-scale randomized trials, that will prolong patient survival. Therefore, establishing an early diagnosis in a premetastatic phase of tumor development must be the overriding goal of any intervention strategy that seeks to reduce CM-related mortality. Unfortunately, as a result of public messages that emphasize the role of ultraviolet radiation (UVR) exposure in tumor development, most general physicians and lay people believe that most if not all cases of CM are the direct result of UVR exposure. In fact, we do not know the case fraction of CM directly attributable to UVR, and the unintended consequences of current messages directly linking UVR exposure and CM development may be thwarting the primary intervention goal of reducing tumor-related mortality. More likely to have an immediate positive impact on CM-related mortality are public messages that encourage skin awareness and self-examination by patients, total skin screening examinations by physicians during routine care, and periodic lifetime surveillance of patients determined to have a high CM risk based on identifiable historic and phenotypic traits.
Similar articles
-
Cutaneous melanoma: public health approach to early detection.Dermatol Ther. 2006 Jan-Feb;19(1):26-31. doi: 10.1111/j.1529-8019.2005.00053.x. Dermatol Ther. 2006. PMID: 16405567 Review.
-
A randomized trial to improve early detection and prevention practices among siblings of melanoma patients.Cancer. 2006 Aug 15;107(4):806-14. doi: 10.1002/cncr.22050. Cancer. 2006. PMID: 16832795 Clinical Trial.
-
Diagnosis and treatment of cutaneous melanoma: state of the art 2006.Melanoma Res. 2007 Apr;17(2):117-27. doi: 10.1097/CMR.0b013e328042bb36. Melanoma Res. 2007. PMID: 17496787 Review.
-
Melanoma. Screening and education.Clin Plast Surg. 2000 Jul;27(3):317-22, vii. Clin Plast Surg. 2000. PMID: 10941555 Review.
-
Evaluation of factors associated with skin self-examination.Cancer Epidemiol Biomarkers Prev. 1999 Nov;8(11):971-8. Cancer Epidemiol Biomarkers Prev. 1999. PMID: 10566551
Cited by
-
Short and long-term barriers and facilitators of skin self-examination among individuals diagnosed with melanoma.BMC Cancer. 2020 Feb 14;20(1):123. doi: 10.1186/s12885-019-6476-5. BMC Cancer. 2020. PMID: 32059700 Free PMC article.
-
Long-term follow-up for melanoma patients: is there any evidence of a benefit?Surg Oncol Clin N Am. 2015 Apr;24(2):359-77. doi: 10.1016/j.soc.2014.12.012. Epub 2015 Jan 24. Surg Oncol Clin N Am. 2015. PMID: 25769718 Free PMC article. Review.
-
Barriers and facilitators of adherence to medical advice on skin self-examination during melanoma follow-up care.BMC Dermatol. 2013 Mar 1;13:3. doi: 10.1186/1471-5945-13-3. BMC Dermatol. 2013. PMID: 23448249 Free PMC article.
-
Contemporary diagnostic imaging modalities for the staging and surveillance of melanoma patients: a meta-analysis.J Natl Cancer Inst. 2011 Jan 19;103(2):129-42. doi: 10.1093/jnci/djq455. Epub 2010 Nov 16. J Natl Cancer Inst. 2011. PMID: 21081714 Free PMC article.
-
Unusually stable abnormal karyotype in a highly aggressive melanoma negative for telomerase activity.Mol Cytogenet. 2008 Aug 22;1:20. doi: 10.1186/1755-8166-1-20. Mol Cytogenet. 2008. PMID: 18718029 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous