Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
Sekisui Diagnostics

Download Mobile App




Gene Expression Test Supports Metastatic Risk Assessment in Melanoma

By LabMedica International staff writers
Posted on 02 Jul 2026

Accurate metastatic risk assessment in early-stage cutaneous melanoma is essential for guiding sentinel lymph node biopsy and follow-up decisions, particularly in patients with stage IB tumors such as T1b and T2a lesions. More...

A gene expression profiling test has now received FDA Breakthrough Device Designation and is included in NCCN Guidelines to support metastatic risk assessment and clinical decision-making in this population.

Merlin CP-GEP, a clinicopathologic gene expression profile (CP-GEP) test from SkylineDx (Rotterdam, Netherlands), is designed to support risk assessment and clinical decision-making in patients with early-stage cutaneous melanoma. The FDA granted Breakthrough Device Designation to Merlin CP-GEP, recognizing its potential to address a significant unmet clinical need. It is positioned as the first and only melanoma gene expression profiling (GEP) test both designated as an FDA Breakthrough Device and included in the National Comprehensive Cancer Network (NCCN) Guidelines for T1b and T2a melanoma within stage IB disease.

The test functions as a non-invasive prediction model that integrates clinicopathologic variables with gene expression profiling in a single algorithm. It provides a binary stratification of patients into High- or Low-Risk for metastasis. Based on this result, patients are assigned to surgical action categories aligned with evidence-based treatment, prevention, and screening guidelines.

The Breakthrough Devices Program is intended to expedite the development and review of technologies that may provide more effective diagnosis or management of life-threatening or irreversibly debilitating diseases. The designation for Merlin CP-GEP is supported by data from MERLIN_001, highlighted as the largest prospective, multi-center, blinded clinical trial in cutaneous melanoma. When used with established clinical criteria, Merlin CP-GEP supports selection for sentinel lymph node biopsy, may inform follow-up discussions, and facilitates shared decision-making between providers and patients.

“Breakthrough Device Designation underscores the potential of Merlin CP-GEP to advance personalized melanoma care and support more informed, patient-centered treatment decisions. Patients deserve access to the best available tools supported by rigorous clinical evidence and recognized in clinical practice guidelines,” said Dharminder Chahal, Chief Executive Officer of SkylineDx.

Related Links
SkylineDx


Platinum Member
Automated Coagulation Analyzer
Hemolumi H6
Gold Member
Quantitative POC Immunoassay Analyzer
EASY READER+
Urine Analyzer
respons® UDS100
New
Gastrointestinal Panel
Xpert® GI Panel
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Technology

view channel
Image: The laser-based photoacoustic spectroscopy setup consists of a Mid-IR laser equipped with three QCL modules covering wavelengths from 5.6 μm to 12.9 μm, two silver coated mirrors (SCM), a dichroic mirror (DM) with a transmittance of 90%, a thermal power sensor head (PM) to monitor the output laser power, a mechanical chopper (MC) for frequency modulation and a CEPAS-detector with a self-designed swab holder (SH). (Credit: Graunke, T., Scholz, T., Pieniak, M. et al. Scientific Reports (2026). https://doi.org/10.1038/s41598-026-68298-9)

Laser-Based Swab Analysis Shows Promise for Detecting Disease-Linked Odor Patterns

Disease-related changes in volatile organic compounds can alter body odor, producing measurable patterns in exhaled breath and bodily fluids. Current analytical methods can be complex, time-consuming,... Read more

Industry

view channel
Image: The acquisition of Proscia advances Agilent’s efforts to expand its pathology portfolio and strengthens its competitive position in a rapidly growing market.

Agilent Acquisition of Proscia to Advance AI-Enabled Digital Pathology Workflows

Agilent Technologies Inc. has entered into a definitive agreement to acquire Proscia, a provider of digital pathology software for clinical and life-sciences customers. The all-cash transaction is valued... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.