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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
.
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 patientsThe 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