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Home NEWS Science News Cancer

New Genomic Test May Help Melanoma Patients Avoid Lymph Node Biopsy Surgery

Bioengineer by Bioengineer
October 22, 2025
in Cancer
Reading Time: 4 mins read
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In a groundbreaking advancement within oncology, researchers at Mayo Clinic, in collaboration with SkylineDx, have unveiled a novel genomic test that promises to revolutionize the management of melanoma by predicting the likelihood of cancer’s presence in the lymph nodes. Published in the prestigious journal JAMA Surgery, this test harnesses cutting-edge molecular diagnostics to guide therapeutic choices, potentially sparing numerous patients from invasive sentinel lymph node biopsy surgeries.

Melanoma, recognized as the deadliest form of skin cancer, poses significant challenges in early detection and precise staging. Traditional methods necessitate sentinel lymph node biopsy—a surgical procedure requiring general anesthesia—where several lymph nodes are excised and examined histologically for metastatic deposits. Despite its diagnostic value, this surgery is associated with potential complications such as infection, lymphedema, and prolonged recovery, while approximately 80% of these biopsies reveal no cancerous involvement, underscoring the critical need for less invasive yet accurate diagnostic tools.

The innovative Merlin CP-GEP Test—which stands for Clinical-Pathologic Gene Expression Profile—employs a sophisticated algorithm that integrates genomic data derived from eight specific gene expression markers within the melanoma tumor tissue alongside critical clinical parameters like patient age and tumor thickness, measured in millimeters. This amalgamation of molecular and clinical data forms a robust predictive model that estimates the probability of lymphatic metastasis with remarkable accuracy. Uniquely, the test utilizes tumor samples obtained during the initial diagnostic biopsy, eliminating the necessity for additional invasive procedures.

A multicenter prospective clinical trial encompassing 1,761 melanoma patients from nine major U.S. cancer institutions over three years validated the test’s clinical utility. Astonishingly, the test demonstrated that around 93% of individuals classified as low-risk for nodal metastasis truly had no cancer in their lymph nodes. Conversely, approximately 25% of patients identified as high-risk did harbor lymph node involvement. These findings signify an unprecedented stride toward personalized oncologic care, allowing clinicians to tailor interventions grounded in each tumor’s genomic blueprint.

Dr. Tina Hieken, the study’s lead author and a surgical oncologist at the Mayo Clinic Comprehensive Cancer Center, emphasized the transformative potential of this test, stating that its implementation could drastically reduce the necessity for sentinel lymph node biopsies without compromising patient outcomes. By harnessing the tumor’s intrinsic biological signals, clinicians can now stratify patients more precisely, prioritizing surgical interventions for those with demonstrable metastatic risk while alleviating low-risk patients from unnecessary operative morbidities.

Melanoma pathogenesis is complex, involving a cascade of molecular events that modulate tumor growth, invasion, and immune evasion. The Merlin CP-GEP Test capitalizes on this molecular intricacy by decoding the expression profiles of genes implicated in tumor aggressiveness and microenvironmental interactions. This level of nuanced insight transcends conventional histopathological assessments, facilitating a deeper understanding of each tumor’s metastatic potential.

The implications of this personalized approach extend beyond surgical decision-making. Accurate risk stratification is pivotal in determining the need for adjuvant therapies and surveillance strategies, thereby optimizing resource allocation and enhancing patient quality of life. Ongoing research aims to elucidate how integrating the test into routine clinical practice influences long-term outcomes, including recurrence rates and survival metrics.

Moreover, the success of this genomic assay reflects a broader paradigm shift in oncology toward precision medicine—where molecular diagnostics and bioinformatics converge to inform individualized care pathways. As researchers continue to unravel the genomic landscape of melanoma, such assays will likely become integral to multidisciplinary cancer management, heralding an era where treatment is increasingly tailored to the unique genetic and phenotypic profile of each patient’s malignancy.

The study underscores the essential role that cross-institutional collaborations play in accelerating translational research. By combining the expertise of surgical oncologists, dermatologists, molecular biologists, and bioinformaticians, the team has effectively bridged the gap between laboratory discoveries and clinical application. This collaborative model serves as a blueprint for future endeavors seeking to transform cancer care through innovative diagnostic technologies.

Importantly, this test aligns with the Mayo Clinic Comprehensive Cancer Center’s mission to develop pioneering, patient-centered approaches that improve cancer detection, prevention, and treatment. Designated by the National Cancer Institute, the center epitomizes a commitment to excellence in cancer research, exemplified through initiatives like the Merlin CP-GEP Test, which leverages scientific innovation to directly impact clinical practice.

While the sentinel lymph node biopsy remains a valuable tool, especially in complex cases, the advent of gene expression profiling presents a compelling alternative for many patients. This transition could markedly reduce the physical and psychological burden associated with surgery, offering a safer, more efficient path for melanoma staging.

As scientific inquiry continues, researchers anticipate that molecular diagnostics will expand to encompass other cancer types and stages, further refining the precision medicine toolkit. The Merlin CP-GEP Test stands as a testament to this promising trajectory, illuminating a future where cancer care is not only effective but also minimally invasive and inherently personalized.

For medical professionals and patients alike, this genomic test represents hope—offering more clarity, less uncertainty, and a significant step toward conquering melanoma with intelligence and compassion.

Subject of Research: Gene expression profiling to predict sentinel lymph node status in melanoma patients

Article Title: Gene Expression Profile–Based Test to Predict Melanoma Sentinel Node Status

News Publication Date: 22-Oct-2025

Web References:

Mayo Clinic Comprehensive Cancer Center: https://www.mayoclinic.org/departments-centers/mayo-clinic-cancer-center
JAMA Surgery (Study Publication): https://jamanetwork.com/journals/jamasurgery/fullarticle/2840207
National Cancer Institute: https://www.cancer.gov/

References:

Hieken, T. J., et al. (2025). Gene Expression Profile–Based Test to Predict Melanoma Sentinel Node Status. JAMA Surgery.

Keywords: melanoma, sentinel lymph node biopsy, genomic test, gene expression profile, cancer staging, precision medicine, oncology diagnostics, melanoma metastasis, Merlin CP-GEP Test, molecular biomarkers

Tags: cancer predictive modelsgene expression profiling in melanomainvasive surgery avoidanceJAMA Surgery publicationMayo Clinic melanoma researchmelanoma genomic testmelanoma patient managementmelanoma staging challengesmolecular diagnostics in oncologynon-invasive diagnostic toolspersonalized cancer treatment strategiessentinel lymph node biopsy alternatives

Tags: melanoma genomic testMerlin CP-GEP Testmolecular biomarkersNon-invasive cancer diagnosticsnon-invasive cancer stagingPrecision Medicine in Oncologyprecision oncology diagnosticssentinel lymph node biopsy alternativessentinel lymph node biopsy avoidance
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