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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03080948
Other study ID # 17-083
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date March 9, 2017
Est. completion date March 2025

Study information

Verified date April 2024
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators are doing this study to improve our ability to identify which people with many moles on their skin are most likely to develop skin melanoma. The investigators hope to identify features of moles that are associated with melanoma risk. The investigators hope to use this information to customize and tailor melanoma screening to the individual patient based on a better estimate of their individual risk.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 73
Est. completion date March 2025
Est. primary completion date March 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients = 18 years of age - High-risk nevus phenotype (= 50 nevi (= 2mm in size) and = 1 atypical nevus) - First presented to MSKCC for cutaneous melanoma-related care on or after April 2016 - Cases: diagnoses of unequivocal invasive cutaneous melanomas (AJCC Stages I-IV) confirmed by MSKCC pathology on or after April 2016 - Cases: completion of surgical treatment of primary melanoma - Ability to sign or verbally consent to the informed consent Exclusion Criteria: - Controls: Histopathologically borderline melanocytic tumors for which melanoma could not be excluded or that were treated as possible melanomas. - Known germline high-penetrance melanoma predisposition mutation (that is, CDKN2A, CDK4, and BAP1) - Cases: history of invasive cutaneous melanoma (AJCC Stages I-IV) not confirmed by MSKCC pathology - History of acrolentiginous type of cutaneous melanoma or history of mucosal melanoma - Cases and controls: prior administration of systemic medications known to modify nevus phenotype, including but not limited to: MEK inhibitors (trametinib, cobimetinib, etc.), BRAF inhibitors (vemurafenib, dabrafenib, etc.), and immunotherapy (pembrolizumab, nivolumab, atezolizumab, ipilimumab, etc.). Controls: history of Stage 0-IV melanoma confirmed by MSKCC pathology - History of limb amputation or other condition (e.g., tattoos, burns) per investigator discretion that would modify nevus phenotype - Physical inability to undergo total body photography or reflectance confocal microscopy imaging (that is, remain relatively still for durations of 3-5 minutes) - Known hypersensitivity to adhesive rings used for reflectance confocal microscopy - Inability to give informed consent - Have skin afflicted with anther skin condition (for example, psoriasis) that would affect ability to characterize nevus phenotype (per investigator discretion) - Familial cutaneous melanoma history (families with at least one invasive melanoma and two or more other diagnoses of invasive melanoma or pancreatic cancer among first- or second-degree relatives on the same side of the family). We will confirm melanoma family history via medical record documentation, whenever possible, as recommended by previous studies that disproved about half of the reported family histories of melanoma among first-degree relatives in case-control studies. - Age 70 or above

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
survey
Research assessments as part of this protocol will be scheduled during routine clinic visits
Other:
Saliva samples
Germline DNA analysis

Locations

Country Name City State
United States Memorial Sloan Kettering Basking Ridge Basking Ridge New Jersey
United States Memorial Sloan Kettering Westchester Harrison New York
United States Memorial Sloan Kettering Cancer Center Hauppauge Hauppauge New York
United States Memorial Sloan Kettering Cancer Center New York New York

Sponsors (4)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center Princess Alexandra Hospital, Brisbane, Australia, Sheba Medical Center, Tel-Aviv Sourasky Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of patients having specific dermoscopic patterns For each person, the proportions of their nevi having specific dermoscopic patterns will be calculated. 2 years