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仑伐替尼治疗碘难治性分化型甲状腺癌患者 8 周相对剂量强度的预后意义。

Prognostic significance of 8 weeks' relative dose intensity of lenvatinib in treatment of radioiodine-refractory differentiated thyroid cancer patients.

机构信息

Department of Medical Oncology, The Cancer Institute Hospital of The Japanese Foundation for Cancer Research, Tokyo, Japan.

Department of Head and Neck Oncology, The Cancer Institute Hospital of The Japanese Foundation for Cancer Research, Tokyo, Japan.

出版信息

Endocr J. 2021 Jun 28;68(6):639-647. doi: 10.1507/endocrj.EJ20-0754. Epub 2021 Jan 28.

Abstract

Lenvatinib is a standard therapy for radioiodine-refractory differentiated thyroid cancer (RR-DTC). However, because of the high incidence of adverse events resulting from this treatment, it is not easy to maintain the dose intensity of lenvatinib, especially in Japanese patients. Although the prognostic impact of lenvatinib dose interruption has been reported, the target dose intensity of lenvatinib to optimize survival benefits remains unknown. We therefore propose a target dose intensity of lenvatinib during the first 8 weeks of treatment. We retrospectively analyzed 42 RR-DTC patients who were treated with lenvatinib for more than 8 weeks. We performed receiver operating characteristic curve analysis to determine the cut-off value of 8 weeks' relative dose intensity (8w-RDI) to predict treatment response, and identified that the optimal cut-off value of 8w-RDI was 60% (sensitivity: 81.8%; specificity: 80.6%). Median progression-free survival (PFS) (not reached [NR] vs. 11.0 months; hazard ratio [HR] 0.29; 95% confidence interval [CI] 0.11-0.72; p < 0.01) and overall survival (NR vs. 27.6 months; HR 0.44; 95% CI 0.11-0.91; p = 0.03) were longer in the higher 8w-RDI (≥60%) patients than in the lower 8w-RDI (<60%) patients. Multivariate analysis revealed that 8w-RDI at ≥60% was an independent prognostic factor for PFS (HR 0.29; 95% CI 0.09-0.96; p = 0.04). Targeting for ≥60% of the relative dose intensity during the first 8 weeks of lenvatinib treatment can be sufficient to achieve significant tumor shrinkage and prolong PFS in RR-DTC patients.

摘要

仑伐替尼是治疗碘难治性分化型甲状腺癌(RR-DTC)的标准疗法。然而,由于这种治疗会引起较高的不良反应发生率,因此不易维持仑伐替尼的剂量强度,尤其是在日本患者中。虽然已有研究报道仑伐替尼剂量中断对预后的影响,但优化生存获益的仑伐替尼目标剂量强度仍不清楚。因此,我们提出了仑伐替尼治疗的前 8 周的目标剂量强度。我们回顾性分析了 42 例接受仑伐替尼治疗超过 8 周的 RR-DTC 患者。我们进行了受试者工作特征曲线分析,以确定 8 周相对剂量强度(8w-RDI)的截断值来预测治疗反应,并确定 8w-RDI 的最佳截断值为 60%(敏感性:81.8%;特异性:80.6%)。较高 8w-RDI(≥60%)患者的中位无进展生存期(PFS)(未达到[NR]与 11.0 个月;风险比[HR]0.29;95%置信区间[CI]0.11-0.72;p<0.01)和总生存期(NR 与 27.6 个月;HR 0.44;95%CI 0.11-0.91;p=0.03)均长于较低 8w-RDI(<60%)患者。多变量分析显示,8w-RDI≥60%是 PFS 的独立预后因素(HR 0.29;95%CI 0.09-0.96;p=0.04)。在仑伐替尼治疗的前 8 周,将相对剂量强度目标设定为≥60%,足以使 RR-DTC 患者的肿瘤显著缩小并延长 PFS。

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