A Prospective Multicenter Sample Collection Study Using Non-invasive Methods to Investigate Mutation Burden in Non-lesional Facial Skin of Patients With a Hx of Skin Cancer
Study Details
Study Description
Brief Summary
This is a prospective, multicenter, sample collection study using DermTech's non-invasive skin collection kits to evaluate the mutation burden of non-lesional facial skin from subjects with a documented history of numerous basal cell carcinomas, squamous cell carcinomas or melanomas compared to that of subjects with no history of skin cancer matched for age, sex and Fitzpatrick phototype.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
This is a prospective, multicenter, sample collection study using DermTech's non-invasive skin collection kits to evaluate the mutation burden of non-lesional facial skin from subjects with a documented history of numerous basal cell carcinomas, squamous cell carcinomas or melanomas compared to that of subjects with no history of skin cancer matched for age, sex and Fitzpatrick phototype.
Approximately 20-30 participants will be enrolled in each of six (6) main groups outlined below for a total of 120-180 subjects and controls:
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Immunocompetent BCC Subjects BCC-predominant group |
Other: Observational Study Only
Non-invasive Skin Sampling
Other Names:
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| Immunocompetent SCC Subjects SCC-predominant group |
Other: Observational Study Only
Non-invasive Skin Sampling
Other Names:
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| Immunocompetent MM Subjects Melanoma group |
Other: Observational Study Only
Non-invasive Skin Sampling
Other Names:
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| Control age, sex and Fitzpatrick phototype match |
Other: Observational Study Only
Non-invasive Skin Sampling
Other Names:
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| Solid Organ Transplantation Recipient - SC At least 5 skin cancers and at least 5 years post-transplant |
Other: Observational Study Only
Non-invasive Skin Sampling
Other Names:
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| Solid Organ Transplantation Recipient No more than 1 skin cancer and at least 5 years post-transplant |
Other: Observational Study Only
Non-invasive Skin Sampling
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Evaluate genomic changes associated with increased risk of skin cancers [1- year]
Non-invasively assess skin samples collected from facial skin from participants with a history of non-melanoma skin cancers and melanoma skin cancer compared to age, sex and Fitzpatrick phototype controls
Secondary Outcome Measures
- Evaluate the potential differences in the number and/or type of mutations in non-lesional skin in solid organ transplant recipients [1-year]
Non-invasively assess skin samples collected from facial skin from solid organ transplant recipients.
Eligibility Criteria
Criteria
Inclusion Criteria:
For the immunocompetent (non-SOTR) groups, a subject will be eligible if he or she:
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Is at least 18 years of age;
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Is willing to consent to non-invasive adhesive tape sampling and DNA mutation burden analysis;
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Has a history of 10 or more basal cell carcinomas (BCCs) and at least a 10:1 ratio of BCC to other skin cancer types; or
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Has a history of 5 or more squamous cell carcinomas (SCCs) and at least a 5:1 ratio of SCC to other skin cancer types; or
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Has a history of 3 or more melanomas; or
For the immunocompetent controls:
- Has no history of skin cancer but is an age, birth sex, and Fitzpatrick phototype match (control) for an enrolled participant.
For the SOTR groups, a subject will be eligible if he or she:
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Is age 50-70;
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Received a heart, lung, kidney, or liver transplant at least 5 years prior to study enrollment; or
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Has a history of 5 or more keratinocyte carcinomas (BCC or SCC), or a history of 3 or more melanomas following organ transplantation.
For the SOTR controls:
- Is a transplant recipient age 50-70 with no more than 2 keratinocyte carcinomas.
Exclusion Criteria:
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Has applied certain topical medications (corticosteroids, alpha-hydroxy acids, retinoids, antibiotics, etc.) to the skin to be sampled within 30 days of beginning the study;
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Has undergone field therapy for actinic keratoses (e.g. 5-fluorouracil) involving the skin to be sampled within the past 12 months;
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Has a generalized skin disorder not related to skin cancer such as psoriasis, photosensitivity disorder, or eczematous dermatitis affecting the skin to be sampled;
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Has a known allergy to latex rubber or tape adhesives;
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Is currently participating in another investigational study, or has participated in another study within 30 days of initiating the current study;
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Has applied a sunscreen, moisturizer, or other topical to the skin to be sampled that cannot be adequately removed and may therefore compromise sample collection;
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Has clinical findings which the Investigator determines may put the subject at undue risk or may interfere with the study;
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Has undergone phototherapy or used a tanning bed within 3 months of beginning the study;
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Has used systemic retinoids, chemotherapeutics, or immunotherapy within 3 months of beginning the study;
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Has used an immunosuppressive medication within 3 months of study initiation, such as azathioprine, cyclosporine, methotrexate, or any of the immunosuppressive biological therapies (TNF-inhibitors, etc.);
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Is known or suspected to have a cancer predisposition syndrome (CPS), such as Gorlin syndrome / basal cell nevus syndrome, Xeroderma pigmentosum, Ferguson-Smith syndrome, Oculocutaneous albinism, Epidermolysis bullosa, Epidermodysplasia verruciformis, Fanconi anemia, Rombo syndrome, Bazex-Dupre-Christol syndrome, Bloom syndrome, Werner syndrome, Dyskeratosis congenita, Hereditary Breast and Ovarian Cancer (HBOC) syndrome, Lynch syndrome, etc.;
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Is known or suspected to harbor a pathogenic germline mutation within one or more cancer predisposition genes, such as TP53, CDKN2A, NF1, BAP1, DICER1, FH, SDHD, VHL, etc.; and
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Has a history of skin cancer that cannot be verified.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | UPMC | Pittsburgh | Pennsylvania | United States | 15213 |
Sponsors and Collaborators
- DermTech
- University of Pittsburgh
Investigators
- Study Director: James Rock, DermTech
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- DermTech 2022