Clinical Stage 0 Cutaneous Melanoma AJCC v8, Clinical Stage I Cutaneous Melanoma AJCC v8, Clinical Stage II Cutaneous Melanoma AJCC v8
Conditions
Brief summary
This clinical trial tests the addition of preferentially expressed antigen in melanoma (PRAME) immunohistochemical (IHC) staining to standard slow Mohs micrographic surgery (SMMS) for guiding tissue removal in patients with stage 0 to IIc cutaneous melanoma. SMMS is a method of skin cancer removal involving repeated tissue removal and examination under a microscope to ensure the tumor is removed as much as possible while sparing healthy tissue. In SMMS, tissue sections are evaluated to determine whether additional tissue removal is needed. The standard method for evaluating the tissue is by using a specific stain called hematoxylin and eosin (H&E) stains. PRAME is a cancer antigen that is being investigated as a diagnostic marker in certain types of cancer. Adding PRAME IHC analysis to standard SMMS staining methods may improve the accuracy for determining whether additional tissue removal is necessary for patients undergoing SMMS for stage 0 to IIc cutaneous melanoma.
Detailed description
PRIMARY OBJECTIVE: I. To compare the efficacy of PRAME IHC-guided slow Mohs micrographic surgery to routine slow Mohs micrographic surgical practices in patients with melanoma. SECONDARY OBJECTIVE: I. To further evaluate the efficacy of PRAME IHC-guided slow Mohs micrographic surgical practices in patients with melanoma. OUTLINE: Patients undergo standard slow Mohs micrographic surgery with the addition of PRAME IHC analysis per the discretion of the surgeon on study. After completion of study treatment, patients are followed up every 6 months for up to 5 years.
Interventions
DIAGNOSTIC_TESTImmunohistochemistry Staining Method
Undergo Preferentially Expressed Antigen in Melanoma (PRAME) IHC analysis
PROCEDUREMohs Surgery
Undergo slow Mohs micrographic surgery
Sponsors
University of California, Davis
National Cancer Institute (NCI)
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Scheduled for SMMS of cutaneous melanoma (stage 0 through stage IIc per American Joint Committee on Cancer \[AJCC\] criteria) * Age \>= 18 years at time of consent * Initial tumor biopsy is PRAME positive or PRAME testing was not done. PRAME testing must be planned if not done * Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study
Exclusion criteria
* Initial biopsy was PRAME negative * Incarcerated persons * Patient with severe, active co-morbidity that would preclude a SMMS of cutaneous melanoma (stage 0 through stage IIc per AJCC criteria)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Margin status | During slow Mohs micrographic surgery (SMMS) procedure | Margin status (positive, negative, or uncertain) will be evaluated from hematoxylin and eosin (H\&E)/SOX-10 + preferentially expressed antigen in melanoma (PRAME) stained sections versus H\&E/SOX-10 stained sections. For PRAME stained sections, margins will be considered positive when \> 75% PRAME+ malignant cells at the tissue margin are observed. The McNemar's test will be used to compare the margin status between the predetermined gold-standard (i.e., H\&E/SOX-10) and H\&E/SOX-10 + PRAME. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Presence of PRAME+ suprabasilar melanocytes in the tissue sections | During SMMS procedure | Will be reported using descriptive statistics, including frequency tables as appropriate. |
| Density of PRAME+ cells | During SMMS procedure | Will be reported as a quartile system (0% positive, 1-25% positive, 26-50% positive, 51-75% positive and \> 75% positive). Will be reported using descriptive statistics, including frequency tables as appropriate. |
| Number of stages needed for clear margins | During SMMS procedure | Will be reported using descriptive statistics, including frequency tables as appropriate. |
| Local recurrence of the excised melanoma | Up to 5 years following SMMS | Will be reported using descriptive statistics, including frequency tables as appropriate. |
| Incidence of regional and distant metastases | Up to 5 years following SMMS | Will be reported using descriptive statistics, including frequency tables as appropriate. |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORDaniel B Eisen
University of California, Davis
Outcome results
None listed