Adjuvant Therapy for Melanoma: Who, What, When?

Christina T. Loguidice
Published: Friday, Sep 28, 2018
Jeffrey Weber, MD, PhD

Jeffrey Weber, MD, PhD
Melanoma has a high cure rate when diagnosed and treated at an early stage, but patients with high-risk melanomas, including stage III disease, remain at increased risk of recurrence and mortality even after definitive surgical treatment. Adjuvant therapy has the potential to improve long-term outcomes in these patients but remains underutilized. In a study presented at the 2018 American Society of Clinical Oncology Annual Meeting, less than 29% of patients with stage III melanoma received adjuvant therapy.1 This may not be surprising: until recently, the only FDA-approved adjuvant treatment option in this setting was interferon (IFN)-α, a drug with variable efficacy and treatment-limiting toxicities.2 The advent of checkpoint inhibitors and targeted agents have given oncologists more to work with.

More patients than ever before may now be good candidates for adjuvant therapy and derive long-term benefits from it, but new data and expanding treatment options have led to many new questions on how to optimize treatment. During the Peer Exchange, a group of melanoma experts shared their insights on who should undergo completion lymph node dissection, which molecular testing and adjuvant treatments to consider, what staging challenges need to be overcome, and when to implement and stop adjuvant therapy.

Stage III Melanoma: Who's Resectable?

Stage III melanoma is now known to be a heterogenous entity, and the panel noted that not all patients with this disease should receive a completion lymph-node dissection, unlike previously thought. “In the stage III setting, we really have to divide patients into the ones who have microscopic disease in their lymph nodes versus the patients who present with bulky disease and macroscopic disease,” Robert Andtbacka, MD, CM, said, noting that 2 recent studies have shown that patients with microscopic disease can do just as well with ultrasound follow-up.3,4

“One of the caveats with both of these studies was that the amount of tumor in the sentinel lymph node was fairly small. When we think about these patients, we have to remember that most patients had only 1 positive sentinel lymph node,” Andtbacka said. He explained that in his practice, he has found the ultrasound approach to be viable for patients with a low disease burden in their sentinel lymph nodes and that more than half of these patients prefer ultrasound over receiving surgery. In general, he said, he reserves complete lymph-node resection for patients with more extensive disease in their lymph node basin or with melanoma in multiple lymph nodes and that these are the patients with whom he also discusses adjuvant therapy, because of their high risk of local and distant recurrence.

BRAF, PD-L1, or Both: What to Test?

Approximately 50% of advanced melanomas are known to harbor BRAF gene mutations,5 and in patients with BRAF V600–mutated melanoma, targeted therapy with BRAF and MEK inhibitors is associated with significant long-term benefit. The panel agreed that obtaining BRAF mutation status early is important. “We now try to do [BRAF testing] on the majority of patients, because of the decisions to be made in the adjuvant setting,” Omid Hamid, MD, said.
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View Conference Coverage
Online CME Activities
TitleExpiration DateCME Credits
Advances in™ Melanoma: Exploring BRAF/MEK in Adjuvant and Neoadjuvant SettingsSep 28, 20191.5
Medical Crossfire®: What Does Data Tell Us About How to Optimize Checkpoint Inhibitor Strategies Across Lines of Care for Patients with Melanoma?Nov 30, 20191.5
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