Faculty Bibliography

Multispectral analysis devices assess pigmented lesion disorganization at different levels using variable wavelengths of light. Computerized algorithms measure morphologic disorganization of the pigmented skin lesion. Aggregated data of 855 participants investigating the influence of multispectral digital skin lesion analysis (MSDSLA) on practitioner decisions to biopsy pigmented skin lesions revealed the overall sensitivity for detection of melanoma improved from 70% to 88%. Participant specificity increased from 52% to 58% after MSDSLA. Five studies using spectrophotometric intracutaneous analysis scope to evaluate suspicious pigmented skin lesions demonstrated an overall sensitivity and specificity of 85% and 81%, respectively, for the detection of melanoma.

Generalized essential telangiectasia (GET) is a notoriously difficult to treat disorder with no current satisfactory treatments. This case and discussion report the use of 6-mercaptopurine (6-MP) as a successful treatment for GET. Moreover, we show that GET may represent a state of increased angiogenesis, a paradigm shift from the current understanding that these telangiectasias represent dilatations of only pre-existing vessels. This new view of GET may drive others to look at novel agents for treatment

J Drugs Dermatol. 2017;16(3):280-282

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A 31-gene expression profile (GEP) test to predict metastasis risk has been validated with over 900 cutaneous melanoma (CM) tumor samples. The test generates Class 1 (low-risk) or 2 (highrisk) results, which are associated with significantly different 5- year distant metastasis free survival rates (91% versus 57%, resp). 157 dermatologists who attended a national educational dermatology conference were presented with the clinical validity evidence for the 31-GEP test, followed by a description of a 30- year-old male with a thigh lesion that was biopsy confirmed melanoma, without ulceration or atypical features and no family or personal history of skin cancer. They were asked to provide the Breslow thickness (BT; ranging from 0.7-1.5 mm) at which they would recommend sentinel lymph node biopsy (SLNB), oncology referral, or imaging. The majority of respondents (62%, 57%, and 55%, resp) indicated a BT of 1.0 mm as the thickness to manage a patient with each modality, reflecting an adherence to current management guidelines. Respondents were then asked the same question in the context of a Class 1 or Class 2 result. After inclusion of a Class 1 result, responses reflecting the BT inflection points for guiding SLNB, oncology referral and imaging were changed in 23%, 18% and 19% of cases, resp, with risk-appropriate changes (increased BT) of 87%, 83% and 59%. Following addition of a Class 2 outcome to patient characteristics, the initial BT used to guide SLNB, medical oncology referral, and imaging was changed in 47%, 50% and 47% of the responses, resp, with 95%, 84% and 97% of the cases changed in a risk-appropriate direction (decreased BT). The results indicate that the 31-GEP test may have a significant and appropriate impact upon CM patient management while remaining within the context of the established practice guidelines that exist today

BACKGROUND: A significant proportion of patients with American Joint Committee on Cancer (AJCC)-defined early-stage cutaneous melanoma have disease recurrence and die. A 31-gene expression profile (GEP) that accurately assesses metastatic risk associated with primary cutaneous melanomas has been described. OBJECTIVE: We sought to compare accuracy of the GEP in combination with risk determined using the web-based AJCC Individualized Melanoma Patient Outcome Prediction Tool. METHODS: GEP results from 205 stage I/II cutaneous melanomas with sufficient clinical data for prognostication using the AJCC tool were classified as low (class 1) or high (class 2) risk. Two 5-year overall survival cutoffs (AJCC 79% and 68%), reflecting survival for patients with stage IIA or IIB disease, respectively, were assigned for binary AJCC risk. RESULTS: Cox univariate analysis revealed significant risk classification of distant metastasis-free and overall survival (hazard ratio range 3.2-9.4, P < .001) for both tools. In all, 43 (21%) cases had discordant GEP and AJCC classification (using 79% cutoff). Eleven of 13 (85%) deaths in that group were predicted as high risk by GEP but low risk by AJCC. LIMITATIONS: Specimens reflect tertiary care center referrals; more effective therapies have been approved for clinical use after accrual. CONCLUSIONS: The GEP provides valuable prognostic information and improves identification of high-risk melanomas when used together with the AJCC online prediction tool.