CP-GEP (Merlin) gene expression profiling: can my melanoma patient forgo sentinel lymph node biopsy?

被引:2
|
作者
Quattrocchi, Enrica [1 ]
Meves, Elena S. [1 ]
Meves, Alexander [1 ]
机构
[1] Mayo Clin, Dept Dermatol, 200 First St SW, Rochester, MN 55905 USA
关键词
Melanoma; Neoplasm metastasis; Sentinel lymph node biopsy; AMERICAN JOINT COMMITTEE; CUTANEOUS MELANOMA; METASTASIS; RISK; DISSECTION; MULTICENTER; PREDICTORS; ULCERATION; IMMEDIATE; SIGNATURE;
D O I
10.23736/S2784-8671.23.07621-1
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Melanoma risk stratification is crucial for both patients and physicians. Patients want to understand what to expect after diagnosis, and physi-cians need to decide on an appropriate treatment plan. Traditionally, risk stratification has been based on Breslow thickness and sentinel lymph node (SLN) status. However, the introduction of CP-GEP (Merlin) has provided a molecular test that can be performed on primary melanoma diagnostic biopsy tissue, offering additional risk stratification beyond established variables. In this review, we assess the utility of CP-GEP test-ing compared to clinicopathologic variables and SLN status and propose a multilayered approach to selecting patients for adjuvant therapy using CP-GEP technology.
引用
收藏
页码:292 / 301
页数:10
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