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A Robust Discovery Platform for the Identification of Novel Mediators of Melanoma Metastasis
Published on: March 8, 2022
Diagnostic test accuracy meta-analysis of PRAME in distinguishing primary cutaneous melanomas from benign melanocytic
Michał Kunc1, Natalia Żemierowska2,3, Filip Skowronek4
1Department of Pathomorphology, Medical University of Gdańsk, Gdańsk.
Abstract:
PRAME is a novel immunohistochemical marker that aids the diagnosis of melanocytic lesions. Diffuse PRAME positivity suggests melanoma, whereas benign naevi are negative or only weakly positive. However, the factual diagnostic accuracy of PRAME is not well established. Moreover, some studies have suggested that the threshold of 3+/50% positive cells may be more useful in practice than the most widely used cut-off (4+/75% of positive cells). Hence, we performed a systematic review and diagnostic accuracy meta-analysis to evaluate sensitivity, specificity, likelihood ratios and optimal threshold for PRAME in distinguishing benign melanocytic proliferations from melanomas. Twenty-six studies were enrolled into the meta-analysis. A total of 2915 melanocytic lesions were analysed. The optimal threshold for PRAME positivity was estimated at 3.11, which translates into 3+ in practice. Sensitivity and specificity calculated from SROC at the 3+ threshold were 0.735 (0.631-0.818) and 0.915 (0.834-0.958), respectively, compared to 0.679 (0.559-0.957) and 0.957 (0.908-0.981) at the 4+ cut-off. In subgroup analysis, the spitzoid subgroup was characterised by the lowest sensitivity and diagnostic odds ratio of PRAME. Our findings indicate that PRAME immunohistochemistry may serve as an ancillary marker to support the diagnosis of melanoma. Nevertheless, the accuracy of PRAME may be lower in spitzoid neoplasms. Our meta-analysis suggests that the 3+/50% threshold might be more useful in practice than the 4+/75% cut-off, as it shows higher sensitivity with retained satisfactory specificity.
Insights
PRAME immunohistochemistry aids melanoma diagnosis. A meta-analysis suggests a 3+/50% threshold offers better sensitivity than 4+/75% for distinguishing melanoma from benign lesions, especially in non-spitzoid cases.
Area of Science:
- Dermatopathology
- Oncology
- Immunohistochemistry
Background:
- PRAME is a novel marker for diagnosing melanocytic lesions, with diffuse positivity suggesting melanoma.
- The diagnostic accuracy and optimal threshold for PRAME in distinguishing melanoma from benign nevi require further clarification.
- Existing cut-offs (e.g., 4+/75%) may not be the most practical for clinical use.
Approach:
- A systematic review and diagnostic accuracy meta-analysis was conducted.
- Twenty-six studies encompassing 2915 melanocytic lesions were analyzed.
- Sensitivity, specificity, likelihood ratios, and optimal thresholds for PRAME were evaluated.
Key Points:
- The optimal PRAME positivity threshold was estimated at 3.11 (practically 3+/50%), yielding a sensitivity of 0.735 and specificity of 0.915.
- The widely used 4+/75% cut-off showed lower sensitivity (0.679) but higher specificity (0.957).
- Spitzoid neoplasms exhibited the lowest sensitivity and diagnostic odds ratio for PRAME.
Conclusions:
- PRAME immunohistochemistry is a valuable ancillary marker for melanoma diagnosis.
- The 3+/50% threshold appears more clinically useful due to higher sensitivity while maintaining good specificity.
- Diagnostic accuracy of PRAME may be reduced in spitzoid neoplasms, warranting caution in these cases.
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