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塞尔帕替尼在中国晚期RET基因改变的甲状腺癌患者中的疗效和安全性:II期LIBRETTO-321研究结果

Efficacy and safety of selpercatinib in Chinese patients with advanced -altered thyroid cancers: results from the phase II LIBRETTO-321 study.

作者信息

Zheng Xiangqian, Ji Qinghai, Sun Yuping, Ge Minghua, Zhang Bin, Cheng Ying, Lei Shangtong, Shi Feng, Guo Ye, Li Linfa, Chen Lu, Shao Jingxin, Zhang Wanli, Gao Ming

机构信息

Department of Thyroid and Neck Tumor, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin, China.

Department of Head and Neck Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.

出版信息

Ther Adv Med Oncol. 2022 Aug 29;14:17588359221119318. doi: 10.1177/17588359221119318. eCollection 2022.

Abstract

BACKGROUND

Selpercatinib, a highly selective and potent REarranged during Transfection (RET) kinase inhibitor, is effective in advanced -altered thyroid cancer (TC). However, the efficacy and safety in Chinese patients are unknown.

PATIENTS AND METHODS

In the open-label, multi-center phase II LIBRETTO-321 (NCT04280081) study, Chinese patients with advanced solid tumors harboring alterations received selpercatinib 160 mg twice daily. The primary endpoint was objective response rate (ORR; RECIST v1.1) by independent review committee (IRC). Secondary endpoints included duration of response (DoR) and safety. Efficacy was assessed in the primary analysis set [PAS; treated patients with fusion-positive TC or mutant medullary TC (MTC) confirmed by central laboratory] and all enrolled patients with MTC.

RESULTS

Of 77 enrolled patients, 29 had -mutant MTC and one had fusion-positive TC. In the PAS ( = 26), the ORR by IRC was 57.7% [95% confidence interval (CI), 36.9-76.6]. Median DoR was not reached and 93.3% of responses were ongoing at a median follow-up of 8.7 months. In all enrolled MTC patients ( = 29), the ORR by IRC was 58.6% (95% CI, 38.9-76.5). One fusion-positive TC patient treated for 23.4 weeks achieved a partial response at week 8 that was ongoing at cutoff. In the safety population ( = 77), 59.7% experienced grade ⩾3 treatment-emergent adverse events (TEAEs). TEAEs led to dose reductions in 32.5% ( = 25) and discontinuations in 5.2% [ = 4; 3.9% ( = 3) considered treatment related] of patients.

CONCLUSIONS

Selpercatinib showed robust antitumor activity and was well tolerated in Chinese patients with advanced -altered TC, consistent with global data from LIBRETTO-001 (NCT04280081).

CLINICALTRIALSGOV IDENTIFIER

NCT04280081 (first posted Feb 21, 2020).

摘要

背景

塞尔帕替尼是一种高度选择性且强效的转染期间重排(RET)激酶抑制剂,对晚期改变的甲状腺癌(TC)有效。然而,其在中国患者中的疗效和安全性尚不清楚。

患者与方法

在开放标签、多中心II期LIBRETTO - 321(NCT04280081)研究中,患有 改变的晚期实体瘤中国患者接受塞尔帕替尼每日两次,每次160mg。主要终点是独立审查委员会(IRC)评估的客观缓解率(ORR;RECIST v1.1)。次要终点包括缓解持续时间(DoR)和安全性。在主要分析集[PAS;经中心实验室确认的融合阳性TC或突变型髓样TC(MTC)的治疗患者]和所有入组的MTC患者中评估疗效。

结果

77例入组患者中,29例患有 -突变型MTC,1例患有 融合阳性TC。在PAS( = 26)中,IRC评估的ORR为57.7%[95%置信区间(CI),36.9 - 76.6]。未达到中位DoR,在中位随访8.7个月时,93.3%的缓解仍在持续。在所有入组的MTC患者( = 29)中,IRC评估 的ORR为58.6%(95%CI,38.9 - 76.5)。1例接受治疗23.4周的 融合阳性TC患者在第8周达到部分缓解,至截止时仍在持续。在安全性人群( = {77})中,59.7%的患者发生≥3级治疗中出现的不良事件(TEAE)。TEAE导致32.5%( = 25)的患者剂量减少,5.2%[ = 4;3.9%( = {3})被认为与治疗相关]的患者停药。

结论

塞尔帕替尼在患有晚期 改变的TC中国患者中显示出强大的抗肿瘤活性且耐受性良好,与LIBRETTO - 001(NCT04280081)的全球数据一致。

临床试验注册号

NCT04280081(首次发布于2020年2月21日)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56d5/9434679/27063b9d2b11/10.1177_17588359221119318-fig1.jpg

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