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    Home > Active Ingredient News > Antitumor Therapy > Clin Cancer Res: Efficacy of Phase 3 Levatinib in Chinese Patients with Radioiodine-Refractory Differentiated Thyroid Cancer

    Clin Cancer Res: Efficacy of Phase 3 Levatinib in Chinese Patients with Radioiodine-Refractory Differentiated Thyroid Cancer

    • Last Update: 2021-08-04
    • Source: Internet
    • Author: User
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    In a phase 3 SELECT study in many countries, Lenvatinib showed an effective treatment for radioiodine-refractory differentiated thyroid cancer (RR-DTC); however, lenvatinib was used in RR-DTC patients in China The efficacy of in has not been verified
    .
    Data in recent years indicate that there are approximately 194,000 confirmed thyroid cancer patients in China


    .


    Radioiodine refractory differentiated thyroid cancer (RR-DTC)Radioiodine refractory differentiated thyroid cancer (RR-DTC)

    This study aims to evaluate the efficacy and safety of lenvatinib in Chinese patients with RR-DTC
    .

    To evaluate the efficacy and safety of lenvatinib in Chinese patients with RR-DTC

    Chinese patients (n=151) diagnosed with RR-DTC were recruited and randomly divided into two groups at a 2:1 ratio, receiving levatinib (24 mg/day, n=103) or placebo (n=48) ) Treatment, every 28 days is a course of treatment
    .
    The primary endpoint is progression-free survival (PFS); key secondary endpoints include objective response rate and safety


    .


    Progression-free survival of the two groups of patients

    Progression-free survival of the two groups of patients

    The progression-free survival of the lenvatinib group was significantly longer than that of the placebo group (median PFS: 23.
    9 vs 3.
    7 months; hazard ratio [HR] 0.
    16, 95%CI 0.
    10-0.
    26; p<0.
    0001)
    .
    The objective response rates of the lenvatinib group and the placebo group were 69.


    9% and 0%, respectively


    The progression-free survival period of the lenvatinib group was significantly longer than that of the placebo group .


    In summary, compared with placebo, lenvatinib (24 mg/day) can also significantly improve the progression-free survival and objective remission rate of Chinese RR-DTC patients
    .
    There is no new or unexpected toxicity


    .


    Compared with placebo, lenvatinib (24 mg/day) can also significantly improve the progression-free survival and objective response rate of Chinese RR-DTC patients.


    Original source:

    Xiangqian Zheng, et al.


    A randomized, phase 3 study of lenvatinib in Chinese patients with radioiodine-refractory differentiated thyroid cancer in this message
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