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Tertiary Care Experience of Sorafenib in the Treatment of Progressive Radioiodine-Refractory Differentiated Thyroid Carcinoma: A Korean Multicenter Study

机译:索拉非尼在进行性放射性碘难治性分化型甲状腺癌治疗中的三级护理经验:韩国多中心研究

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摘要

>Background: Sorafenib, a multi-kinase inhibitor, is approved for the treatment of patients with radioactive iodine (RAI)-refractory differentiated thyroid cancer (DTC). This study evaluated the efficacy and safety of sorafenib in real-world clinical practice and compared the results to those of the DECISION trial. The clinical features associated with better clinical outcomes after sorafenib treatment were also evaluated.>Methods: This multicenter, retrospective cohort study evaluated 98 patients with progressive RAI-refractory DTC who were treated with sorafenib in six tertiary hospitals in Korea. The primary objective was the progression-free survival (PFS) according to Response Evaluation Criteria In Solid Tumors v1.1. Overall survival, response rate (defined as the best objective response according to Response Evaluation Criteria In Solid Tumors v1.1), and safety were also evaluated.>Results: The median PFS was 9.7 months; median overall survival was not reached during follow-up. Partial responses and stable disease were achieved in 25 (25%) and 64 (65%) patients, respectively. Stable disease of >6 months was achieved in 41 (42%) patients. Subgroup analyses identified several prognostic indicators of a better PFS: absence of disease-related symptoms (hazard ratio [HR] = 0.5; p = 0.041), lung-only metastasis (HR = 0.4; p = 0.048), a daily maintenance dose ≥600 mg (HR = 0.3; p = 0.005), and a thyroglobulin reduction ≥60% (HR = 0.4; p = 0.012). The mean daily dose of sorafenib was 666 ± 114 mg, and drug withdrawals due to adverse events (AEs) occurred in 13% of patients. AEs and serious AEs were reported in 93 (95%) and 40 (41%) patients, respectively. The most frequent AE was hand-foot skin reaction (76%).>Conclusions: The PFS of progressive RAI-refractory DTC patients treated with sorafenib was consistent with the findings of the DECISION trial. Disease-related symptoms, lung-only metastasis, a daily maintenance dose, and thyroglobulin reduction were significantly associated with PFS. These results suggest that sorafenib is an effective treatment option for patients with progressive RAI-refractory DTC.
机译:>背景:索拉非尼是一种多激酶抑制剂,已被批准用于治疗放射性碘(RAI)-难治性分化型甲状腺癌(DTC)患者。这项研究评估了索拉非尼在实际临床实践中的疗效和安全性,并将结果与​​DECISION试验的结果进行了比较。 >方法:该多中心回顾性队列研究评估了韩国六家三级医院中98例接受索拉非尼治疗的进展性RAI难治性DTC患者。 。主要目标是根据实体瘤反应评估标准v1.1中的无进展生存期(PFS)。还评估了总生存期,缓解率(根据《实体肿瘤缓解评估标准》 v1.1定义为最佳客观缓解)和安全性。>结果:中位PFS为9.7个月;随访期间未达到中位总生存期。 25例(25%)和64例(65%)的患者分别获得了部分反应和稳定的疾病。 41名(42%)患者实现了> 6个月的稳定疾病。亚组分析确定了PFS更好的几个预后指标:无疾病相关症状(危险比[HR] = 0.5; p = 0.041),仅肺转移(HR = 0.4; p = 0.048),每日维持剂量≥ 600μg(HR = 0.3,p = 0.005),甲状腺球蛋白减少≥60%(HR = 0.4; p = 0.012)。索拉非尼的日平均剂量为666±±114μg,13%的患者因不良事件(AE)停药。据报道,分别有93名患者(95%)和40名患者(41%)发生了AE和严重AE。 AE最常见的是手足皮肤反应(76%)。>结论:索拉非尼治疗的进行性RAI难治性DTC患者的PFS与DECISION试验的结果一致。疾病相关症状,仅肺转移,每日维持剂量和甲状腺球蛋白减少与PFS显着相关。这些结果表明索拉非尼是进行性RAI难治性DTC患者的有效治疗选择。

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