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Cancer Resources and Clinical Trials
Cancer Resources
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Clinical Trials
Maroone Cancer Center is participating in a clinical trial to evaluate the impact of the DecisionDx®-Melanoma gene expression profile on sentinel lymph node biopsy decisions and clinical outcomes.
Until recently, physicians have relied on traditional clinical and pathological factors to determine whether melanoma is likely to spread to the lymph nodes and elsewhere in the body. DecisionDx-Melanoma analyzes the genetic profile of an individual patient’s melanoma tissue to gauge the risk of metastasis or recurrence more accurately and determine the need for an invasive sentinel lymph node biopsy. Patients with a positive sentinel lymph node biopsy are at higher risk for recurrence and are considered eligible for immunotherapy to decrease the risk of melanoma recurrence.
“It’s difficult to predict whether early-stage melanoma will spread to the lymph nodes,” explains Maroone Cancer Center oncologist Timmy Nguyen, MD. “You can’t do a biopsy for everyone because the majority of cases will not have melanoma involved in the lymph nodes, and those procedures can cause complications. So, this test is used along with the tissue specimen viewed under a microscope to be a better and more personalized predictor of risk.”
The test results also may guide the intensity of follow-up surveillance after initial surgical removal of the melanoma, Dr. Nguyen adds.
The trial will evaluate the association between use of DecisionDx-Melanoma and sentinel lymph node biopsy decisions, and will track five-year clinical outcomes of patients who undergo the genetic testing. Study participants must be at least 18 years old with newly diagnosed invasive melanoma being considered for sentinel lymph node biopsy.
Anyone interested in participating in the trial should contact Sharon Lew, MHA, CCRP, Cancer Clinical Research Program Supervisor at Maroone Cancer Center, at lews2@ccf. org. For more information, visit ClevelandClinicFlorida.org/