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RecruitingNCT06673095

Narrow Excision Versus Wide Excision for the Treatment of Adults With Invasive Cutaneous Melanoma, ICEMAN Trial

ICEMAN (Intelligent Choice of Excision Margin): A Randomized Controlled Trial of Narrow Excision Versus Wide Excision for Adults With Primary Invasive Cutaneous Melanomas

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
1,000 (estimated)
Sponsor
OHSU Knight Cancer Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This clinical trial compares the effect of a narrow surgical excision (removal) to a wide excision for the treatment of adults with invasive cutaneous melanoma. Currently the standard of care is to take wide margins (boarder of healthy tissue surrounding the melanoma) when removing melanoma. Narrow margin excision removes a smaller amount of healthy tissue when surgically removing the melanoma. Narrow margin excision may be effective in removing the melanoma while also reducing surgical complications and improving quality of life for adults with invasive cutaneous melanoma.

Detailed description

PRIMARY OBJECTIVE: I. To compare the 3-year local recurrence-free survival rates (RFS) in melanoma patients treated with narrow excision versus (vs) wide excision. SECONDARY OBJECTIVES: I. To measure the 3-, 5-year Regional (nodal) disease-free survival (DFS) in melanoma patients treated with active nodal surveillance. II. To compare 5-year local recurrence-free survival in patients treated with narrow vs wide excision. III. To compare 5-year Melanoma Specific Survival (MSS) in patients treated with narrow vs wide excision. IV. To compare the quality of life in patients treated with narrow vs wide excision. V. To compare surgical complication rates in patients treated with narrow vs wide excision. VI. To compare the frequency of complex reconstruction in patients treated with narrow vs wide excision. VII. To compare the final defect size in patients treated with narrow vs wide excision. VIII. To compare the number of operative/procedure days required to achieve negative margins. EXPLORATORY OBJECTIVE: I. To measure the T- and B-cell repertoires in patients with melanoma over time. OUTLINE: Patients are randomized to 1 of 2 arms. ARM I: Patients undergo narrow margin excision on study. Patients may optionally undergo blood sample collection throughout the study. ARM II: Patients undergo wide margin excision on study. Patients may optionally undergo blood sample collection throughout the study. After completion of study treatment, patients are followed up at 1 week, 3, 6, 12, 36, 48, and 60 months.

Conditions

Interventions

TypeNameDescription
PROCEDUREBiospecimen CollectionUndergo blood sample collection
PROCEDUREExcisionUndergo narrow margin excision
PROCEDUREExcisionUndergo wide margin excision
OTHERSurvey AdministrationAncillary studies

Timeline

Start date
2024-12-11
Primary completion
2027-12-31
Completion
2027-12-31
First posted
2024-11-04
Last updated
2026-03-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06673095. Inclusion in this directory is not an endorsement.