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PRAME Immunohistochemistry as an Adjunct for Evaluating Ambiguous Melanocytic Proliferation

PRAME Immunohistochemistry as an Adjunct for Evaluating Ambiguous Melanocytic Proliferation

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05089188
Acronym
ANTIPRAME
Enrollment
55
Registered
2021-10-22
Start date
2021-11-30
Completion date
2022-11-30
Last updated
2021-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Melanoma

Keywords

Immunohistochemistry, Histopathology

Brief summary

Skin melanoma is a common form of skin cancer. Its diagnosis is usually clinically suspected and then affirmed by histopathological examination. In some cases, the histopathological analysis of these lesions is equivocal, and the malignant or benign nature of the proliferation is difficult to determine with certainty. In these cases, the use of expensive ancillary tests, which are hardly accessible and take a long time to set up (FISH - CGH-array), is usually required. Anti-PRAME immunostaining, an inexpensive and readily available technic, has recently been described as highly sensitive and specific for diagnosing malignant melanocytic proliferations. Knowledge on its utility for evaluating ambiguous melanocytic neoplasms remains limited. Our study aims to improve the current body of knowledge on the utility of PRAME immunohistochemistry for evaluating challenging samples of melanocytic proliferation. The secondary objective is to determine the PRAME immunoreactivity profile for each histological subtype of melanocytic proliferations (spitzoid tumors, cellular blue nevi, dysplastic nevi ...)

Interventions

OTHERImmunomarkers

immunohistochemical expression profile of ambiguous melanocytic proliferation.

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patient at the time of diagnosis (\> = 18 years). * histopathological diagnosis of ambiguous melanocytic proliferation or atypical melanocytic proliferation made between January 2016 and December 2020. * Histological slides archived in the CRB biobank available * Formalin-fixed paraffin-embedded tissue block archived in the CRB biobank available * Informed patient

Exclusion criteria

* Patient who has expressed opposition to participating in the study.

Design outcomes

Primary

MeasureTime frameDescription
Immunomarkers1 monthCorrelation of melanocytic lesions' histopathological diagnosis concerning benignity or malignancy with anti-PRAME immunohistochemical expression profile

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026