Elsevier

Dermatologic Clinics

Volume 30, Issue 3, July 2012, Pages 535-545
Dermatologic Clinics

New Diagnostic Aids for Melanoma

https://doi.org/10.1016/j.det.2012.04.012Get rights and content

Introduction

According to estimates, there will be approximately 70,000 new cases of melanoma and 8800 subsequent deaths in 2011. For 2012 the estimates are 76,250 cases and 9180 deaths.1 The incidence of melanoma has been steadily increasing and has doubled in recent decades.2 For lesions with a depth of less than 1 mm, surgical excision is usually curative and 5-year survival rate is 93% to 97%.3 By contrast, distant metastatic melanoma has an extremely poor prognosis and 5-year survival ranges from 10% to 20%, depending on location of the metastasis.3 Detection of melanoma at an early stage is critical for improving the survival rate. In addition to decreased survival of late-stage versus early-stage melanoma, the cost of treating a late-stage melanoma is dramatically higher. Recent estimates show the total costs of in situ tumors to be around $4700, whereas a stage IV melanoma has a total cost of approximately $160,000.4 The cost of treating late-stage melanoma is likely to increase with the implementation of newly approved treatments such as ipilimumab, which costs about $120,000 for a full treatment.

Despite advances in diagnostic aids such as dermatoscopy, detection has remained a significant challenge, and improved methods of accurately diagnosing melanoma are needed. Studies have shown that even for expert dermoscopists, accurately diagnosing melanoma, particularly in small-diameter lesions, is very challenging, with one study showing a biopsy sensitivity of 71% for melanomas of size less than 6 mm.5 To measure specificity, numerous studies have looked at biopsy ratios (ie, the number of biopsies of benign lesions performed to make the diagnosis of one skin cancer), and numbers vary widely. On the low end, a study from a specialized pigmented lesion clinic showed a biopsy ratio of approximately 5:1 (5 benign lesions per melanoma biopsied).6 A recent retrospective study involving 8 practitioners at a single institution had a biopsy ratio of 15:1.7 On the high end, a study involving a single physician over a 14-year period showed a biopsy ratio of more than 500:1 in patients with no history of melanoma.8 Given these challenges, new diagnostic aids that could help increase both sensitivity and specificity of biopsies would be of great benefit to patients and physicians. Such improvements (Table 1) have the potential to lead to increased diagnosis of early lesions, which would improve survival and lower the overall cost of treating melanoma. In addition, improved diagnostic techniques would lead to fewer biopsies and decreased morbidity to patients.

Section snippets

Physician and Patient Detection of Malignant Melanoma

Multiple studies have tried to assess who initially detects melanomas, with most finding that the majority of melanomas are detected by the patient.9, 10, 11 Patient education, including the ABCDEs (Asymmetry, Border irregularity, Color variegation, Diameter of >6 mm, and Evolution) of melanoma will always be an important part of helping patients to diagnose melanoma.12, 13 In addition, regular self-examinations of the skin should be encouraged, as they have been associated with detection of

Confocal Scanning Laser Microscopy

Confocal scanning laser microscopy (CSLM) is a noninvasive imaging technology that provides in vivo images of the epidermis and papillary dermis in real time. There are currently 2 forms of CSLM in use: reflectance mode, which is primarily used in clinical practice, and fluorescence mode, used primarily in research. Reflectance confocal microscopy (RCM) relies on the inherent reflective properties of tissue structures, whereas fluorescence CSLM relies on fluorescent dyes to provide contrast for

Other imaging technologies

Optical coherence tomography (OCT) is a well-established tool in ophthalmology. OCT is commonly used as a diagnostic aid for uveal melanoma43 and has shown usefulness in dermatology as well. OCT is analogous to ultrasound imaging, except that it uses light rather than sound waves. OCT uses a low-coherence-length light source to evaluate lesion architecture up to 1 mm in depth.44 One study showed that OCT allows for in vivo correlation between dermatoscopic parameters and histopathologic

Noninvasive Genomic Detection

Epidermal genetic information retrieval (EGIR; DermTech International, La Jolla, CA, USA) uses an adhesive tape placed on suspicious lesions to sample cells from the stratum corneum noninvasively. RNA isolated from cells is amplified using real-time polymerase chain reaction and then hybridized with Affymetrix human genome U133 plus 2.0 GeneChip. Gene expression is then analyzed. Using this technology, 312 genes that are differentially expressed between melanoma, nevi, and normal skin were

Summary

Despite recent advances in the diagnosis and treatment of malignant melanoma, it still remains a potentially devastating disease if not diagnosed early and treated properly. With incidence continuing to increase, advances in diagnostic techniques are necessary because diagnosing melanoma is difficult and current methods still miss too many cases, especially in small-diameter lesions. Moreover, biopsying benign lesions can lead to increased morbidity to patients and increased cost to the health

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References (63)

  • T. Hinz et al.

    Real-time tissue elastography: a helpful tool in the diagnosis of cutaneous melanoma?

    J Am Acad Dermatol

    (2011)
  • H. Williams et al.

    Sniffer dogs in the melanoma clinic?

    Lancet

    (1989)
  • J. Church et al.

    Another sniffer dog for the clinic?

    Lancet

    (2001)
  • R Siegel et al.

    Cancer statistics, 2012

    CA Cancer J Clin

    (2012)
  • R Siegel et al.

    Cancer statistics, 2011: the impact of eliminating socioeconomic and racial disparities on premature cancer deaths

    CA Cancer J Clin

    (2011)
  • C.M. Balch et al.

    Final version of 2009 AJCC melanoma staging and classification

    J Clin Oncol

    (2009)
  • D.T. Alexandrescu

    Melanoma costs: a dynamic model comparing estimated overall costs of various clinical stages

    Dermatol Online J

    (2009)
  • R.J. Friedman et al.

    The diagnostic performance of expert dermoscopists vs a computer-vision system on small-diameter melanomas

    Arch Dermatol

    (2008)
  • P. Carli et al.

    Frequency and characteristics of melanomas missed at a pigmented lesion clinic: a registry-based study

    Melanoma Res

    (2004)
  • R.L. Wilson et al.

    How good are US dermatologists at discriminating skin cancers? A number-needed-to-treat analysis

    J Dermatolog Treat

    (2012)
  • M.H. Cohen et al.

    Surgical prophylaxis of malignant melanoma

    Ann Surg

    (1991)
  • M.S. Brady et al.

    Patterns of detection in patients with cutaneous melanoma

    Cancer

    (2000)
  • D.S. Epstein et al.

    Is physician detection associated with thinner melanomas?

    JAMA

    (1999)
  • J. Kantor et al.

    Routine dermatologist-performed full-body skin examination and early melanoma detection

    Arch Dermatol

    (2009)
  • N.R. Abbasi et al.

    Early diagnosis of cutaneous melanoma: revisiting the ABCD criteria

    JAMA

    (2004)
  • D.S. Rigel et al.

    ABCDE—an evolving concept in the early detection of melanoma

    Arch Dermatol

    (2005)
  • M. Berwick et al.

    Screening for cutaneous melanoma by skin self-examination

    J Natl Cancer Inst

    (1996)
  • P. Carli et al.

    Dermatologist detection and skin self-examination are associated with thinner melanomas: results from a survey of the Italian Multidisciplinary Group on Melanoma

    Arch Dermatol

    (2003)
  • R.A. Pollitt et al.

    Efficacy of skin self-examination practices for early melanoma detection

    Cancer Epidemiol Biomarkers Prev

    (2009)
  • L. Trolle et al.

    Ability to self-detect malignant melanoma decreases with age

    Clin Exp Dermatol

    (2011)
  • P. Carli et al.

    Improvement of malignant/benign ratio in excised melanocytic lesions in the ‘dermoscopy era’: a retrospective study 1997-2001

    Br J Dermatol

    (2004)
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    Funding Sources: Dr Ferris: NIH/NCRR grant number 5 UL1 RR024153-04. Dr Harris: None.

    Conflicts of Interest: Dr Ferris: Served as an investigator and consultant for MELA Sciences and as an investigator for DermTech International. Dr Harris: No conflicts of interest to declare.

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