Sentinel node biopsy has proven its value in a number of cancers, including in clinically node-negative melanoma of the head and neck region. However, experts agree that it remains unclear what role sentinel node biopsy should have in other head and neck cancers. Clinical trials are under way to clarify the issue.
Explore this issue:July 2007
Sentinel Node Biopsy in Melanoma
Sentinel node biopsy was initially developed by Donald L. Morton, MD, Chief of the Melanoma Program and Medical Director and Surgeon-in-Chief of the John Wayne Cancer Institute in Santa Monica, CA, and colleagues in the early 1990s. The goal of the procedure is to improve staging of clinically node-negative patients by identifying small metastases in the first lymph node or nodes to which the tumor drains. For tumor types, such as melanoma, that metastasize via the lymphatic system, a negative sentinel node should indicate that the tumor has not spread beyond the initial tumor bed and that all nodes in the nearby basin will be negative. By more effectively identifying patients who have early nodal metastases, the procedure also reduces the number of patients who have to undergo a complete lymphadenectomy.
Results from a large multinational randomized trial indicate that sentinel node biopsy prolongs disease-free survival in patients with intermediate-thickness clinically node-negative melanoma. In the trial, 769 patients had standard surgical resection of the primary tumor and a sentinel node biopsy. If the biopsy showed evidence of disease, the patient had a complete nodal dissection. In the control arm, 500 patients underwent standard tumor resection and regional nodal observation. If a patient subsequently developed a palpable or radiologically detectable nodal metastasis, he or she had a complete lymphadenectomy.