An overview of the standard of care treatment for patients with advanced radioiodine-refractory differentiated thyroid cancer.
Case: A 64-Year-Old Woman with DTC
Initial presentation
Clinical workup and initial treatment
Subsequent treatment and follow-up
This is a video synopsis/summary of a Case-Based Peer Perspective featuring Lori Wirth, MD.
Wirth discusses the National Comprehensive Cancer Network guidelines for patients with progressive radioactive iodine (RAI)–refractory differentiated thyroid cancer (DTC). The guidelines recommend molecular diagnostics whenever possible before initiating therapy due to the availability of gene-specific first-line treatment options, such as larotrectinib or entrectinib for NTRK fusion–positive patients and selpercatinib or pralsetinib for RET fusion–positive disease. Lenvatinib has a preferred category 1 recommendation for progressive RAI-refractory DTC without oncogenic gene fusions, while sorafenib also has a category 1 recommendation.
One challenge in initiating treatment is determining the appropriate timing. Asymptomatic patients with a low disease burden and slow growth may not require immediate therapy, and ongoing disease monitoring and thyroid-stimulating hormone suppression may be the most appropriate approach. However, patients with rapidly progressive RAI-refractory DTC or those likely to develop disease progression symptoms should initiate treatment. Subset analyses from the SELECT trial suggest that symptomatic patients do not respond to treatment, emphasizing the importance of not waiting until symptoms develop before starting therapy.
Video synopsis is AI-generated and reviewed by Targeted Oncology® editorial staff.
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