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EXAM的总生存分析,一项卡博替尼用于放射性进展性甲状腺髓样癌患者的III期试验。

Overall survival analysis of EXAM, a phase III trial of cabozantinib in patients with radiographically progressive medullary thyroid carcinoma.

作者信息

Schlumberger M, Elisei R, Müller S, Schöffski P, Brose M, Shah M, Licitra L, Krajewska J, Kreissl M C, Niederle B, Cohen E E W, Wirth L, Ali H, Clary D O, Yaron Y, Mangeshkar M, Ball D, Nelkin B, Sherman S

机构信息

Department of Nuclear Medicine and Endocrine Oncology, Gustave Roussy and University Paris-Saclay, Villejuif, France.

Endocrine Unit, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

出版信息

Ann Oncol. 2017 Nov 1;28(11):2813-2819. doi: 10.1093/annonc/mdx479.

Abstract

BACKGROUND

Primary analysis of the double-blind, phase III Efficacy of XL184 (Cabozantinib) in Advanced Medullary Thyroid Cancer (EXAM) trial demonstrated significant improvement in progression-free survival with cabozantinib versus placebo in patients with progressive medullary thyroid cancer (MTC). Final analysis of overall survival (OS), a key secondary endpoint, was carried out after long-term follow-up.

PATIENTS AND METHODS

EXAM compared cabozantinib with placebo in 330 patients with documented radiographic progression of metastatic MTC. Patients were randomized (2:1) to cabozantinib (140 mg/day) or placebo. Final OS and updated safety data are reported.

RESULTS

Minimum follow-up was 42 months. Kaplan-Meier analysis showed a 5.5-month increase in median OS with cabozantinib versus placebo (26.6 versus 21.1 months) although the difference did not reach statistical significance [stratified hazard ratio (HR), 0.85; 95% confidence interval (CI), 0.64-1.12; P = 0.24]. In an exploratory assessment of OS, progression-free survival, and objective response rate, cabozantinib appeared to have a larger treatment effect in patients with RET M918T mutation-positive tumors compared with patients not harboring this mutation. For patients with RET M918T-positive disease, median OS was 44.3 months for cabozantinib versus 18.9 months for placebo [HR, 0.60; 95% CI, 0.38-0.94; P = 0.03 (not adjusted for multiple subgroup analyses)], with corresponding values of 20.2 versus 21.5 months (HR, 1.12; 95% CI, 0.70-1.82; P = 0.63) in the RET M918T-negative subgroup. Median treatment duration was 10.8 months with cabozantinib and 3.4 months with placebo. The safety profile for cabozantinib remained consistent with that of the primary analysis.

CONCLUSION

The secondary end point was not met in this final OS analysis from the trial of cabozantinib in patients with metastatic, radiographically progressive MTC. A statistically nonsignificant increase in OS was observed for cabozantinib compared with placebo. Exploratory analyses suggest that patients with RET M918T-positive tumors may experience a greater treatment benefit with cabozantinib.

TRIAL REGISTRATION NUMBER

NCT00704730.

摘要

背景

XL184(卡博替尼)治疗晚期甲状腺髓样癌(EXAM)的双盲III期试验的初步分析表明,对于进展期甲状腺髓样癌(MTC)患者,卡博替尼与安慰剂相比,无进展生存期有显著改善。对总生存期(OS)这一关键次要终点进行了长期随访后的最终分析。

患者与方法

EXAM试验将330例有影像学记录的转移性MTC进展患者的卡博替尼与安慰剂进行比较。患者按2:1随机分组接受卡博替尼(140mg/天)或安慰剂治疗。报告了最终的总生存期和更新的安全性数据。

结果

最短随访时间为42个月。卡普兰-迈耶分析显示,卡博替尼组的中位总生存期比安慰剂组增加了5.5个月(26.6个月对21.1个月),尽管差异未达到统计学显著性[分层风险比(HR),0.85;95%置信区间(CI),0.64 - 1.12;P = 0.24]。在对总生存期、无进展生存期和客观缓解率的探索性评估中,与未携带该突变的患者相比,卡博替尼在RET M918T突变阳性肿瘤患者中似乎具有更大的治疗效果。对于RET M918T阳性疾病患者,卡博替尼组的中位总生存期为44.3个月,而安慰剂组为18.9个月[HR,0.60;95% CI,0.38 - 0.94;P = 0.03(未针对多个亚组分析进行调整)],在RET M918T阴性亚组中相应值为20.2个月对21.5个月(HR,1.12;95% CI,0.70 - 1.82;P = 0.63)。卡博替尼的中位治疗持续时间为10.8个月,安慰剂为3.4个月。卡博替尼的安全性与初步分析一致。

结论

在这项针对转移性、影像学进展性MTC患者的卡博替尼试验的最终总生存期分析中,次要终点未达到。与安慰剂相比,卡博替尼的总生存期虽有增加但无统计学显著性。探索性分析表明,RET M918T阳性肿瘤患者使用卡博替尼可能获得更大的治疗益处。

试验注册号

NCT00704730。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b83/5834040/3d14c0571c77/mdx479f1.jpg

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