Extended Real-World Observation of Patients Treated with Sorafenib for Radioactive Iodine-Refractory Differentiated Thyroid Carcinoma and Impact of Lenvatinib Salvage Treatment: A Korean Multicenter Study

Background: Treatment for patients with radioactive iodine (RAI)-refractory differentiated thyroid carcinoma (DTC) is challenging. Recently, two tyrosine kinase inhibitors (sorafenib and lenvatinib) have been approved and showed benefits for progression-free survival with tolerable adverse events. M...

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Veröffentlicht in:Thyroid (New York, N.Y.) N.Y.), 2019-12, Vol.29 (12), p.184-1810
Hauptverfasser: Oh, Hye-Seon, Shin, Dong Yeob, Kim, Mijin, Park, So Young, Kim, Tae Hyuk, Kim, Bo Hyun, Kim, Eui Young, Kim, Won Bae, Chung, Jae Hoon, Shong, Young Kee, Lim, Dong Jun, Kim, Won Gu
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Sprache:eng
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Zusammenfassung:Background: Treatment for patients with radioactive iodine (RAI)-refractory differentiated thyroid carcinoma (DTC) is challenging. Recently, two tyrosine kinase inhibitors (sorafenib and lenvatinib) have been approved and showed benefits for progression-free survival with tolerable adverse events. Methods: This is an extension study of a previous multicenter, retrospective cohort study of real-world experience in treating 98 patients with progressive RAI-refractory DTC with sorafenib. The primary endpoint was overall survival (OS). The efficacy of lenvatinib as salvage therapy after disease progression on first-line sorafenib was evaluated by comparing outcomes in 32 patients who were treated with lenvatinib with 41 patients who were not and therefore served as a no salvage treatment group. Results: The median OS of all 98 patients treated with sorafenib was 41.5 months, and the median progression-free survival was 13.5 months. Patients without disease-related symptoms before sorafenib treatment had better OS than those with symptoms (hazard ratio [HR] = 0.56 [95% confidence interval, CI 0.31–0.99], p  = 0.048). Larger tumor size was associated with a minimally increased risk of death (HR = 1.02 [CI 1.00–1.03], p  = 0.049). Best tumor response was not associated with OS ( p  = 0.490). Lenvatinib salvage treatment significantly improved OS in patients receiving it compared with those who did not (HR = 0.28 [CI 0.15–0.53], p  
ISSN:1050-7256
1557-9077
DOI:10.1089/thy.2019.0246