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一线塞瑞替尼与克唑替尼治疗间变性淋巴瘤激酶阳性晚期或转移性非小细胞肺癌的疗效比较:与外部对照的调整间接比较。

Comparative efficacy of first-line ceritinib and crizotinib in advanced or metastatic anaplastic lymphoma kinase-positive non-small cell lung cancer: an adjusted indirect comparison with external controls.

机构信息

Analysis Group, Inc., Boston, MA USA.

Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.

出版信息

Curr Med Res Opin. 2019 Jan;35(1):105-111. doi: 10.1080/03007995.2018.1541443. Epub 2018 Nov 15.

DOI:10.1080/03007995.2018.1541443
PMID:30362839
Abstract

In the absence of head-to-head trials, this study indirectly compared progression free survival (PFS) and overall survival (OS) between ceritinib and crizotinib among patients with previously untreated advanced anaplastic lymphoma kinase ()-positive non-small cell lung cancer (NSCLC). A matching-adjusted indirect comparison method was implemented to adjust for cross-trial differences in patient characteristics between ASCEND-4 and PROFILE 1014 trials. Patient-level data from ASCEND-4 and published summary data from PROFILE 1014 were used. Patients in ASCEND-4 were reweighted to match average baseline characteristics (i.e. age, sex, race, tumor histology, ECOG score, smoking status, extent of disease, and presence of brain metastases) reported for PROFILE 1014 patients using propensity score weighting. PFS and OS were then compared between balanced populations. ASCEND-4 included more current smokers (8.0% vs 4.4%) and fewer patients under the age of 65 years (78.5% vs 84.0%) compared to PROFILE 1014. After matching, these and all other patient characteristics were balanced between the two trial populations. Compared to crizotinib, ceritinib was associated with a significantly longer PFS (hazard ratio [95% confidence interval] (HR [CI]) = 0.64 [0.47-0.87]; median PFS: 25.2 vs 10.8 months, log-rank -value = 0.003). OS did not differ significantly, with a HR of 0.82 [0.54-1.27] for ceritinib compared to crizotinib. In the adjusted indirect comparison with external controls, the second generation inhibitor, ceritinib, was associated with a significantly prolonged PFS compared to crizotinib as first-line treatment for -positive NSCLC.

摘要

在缺乏头对头试验的情况下,本研究通过比较 ASCEND-4 与 PROFILE 1014 试验,间接比较了未经治的晚期间变性淋巴瘤激酶(ALK)阳性非小细胞肺癌(NSCLC)患者中塞瑞替尼与克唑替尼的无进展生存期(PFS)和总生存期(OS)。采用匹配调整间接比较法,调整 ASCEND-4 与 PROFILE 1014 试验中患者特征的跨试验差异。使用 ASCEND-4 的患者水平数据和 PROFILE 1014 的已发表汇总数据。使用倾向评分加权法,对 ASCEND-4 中的患者进行重新加权,以匹配 PROFILE 1014 患者报告的平均基线特征(即年龄、性别、种族、肿瘤组织学、ECOG 评分、吸烟状态、疾病程度和脑转移存在)。然后比较平衡人群中的 PFS 和 OS。与 PROFILE 1014 相比,ASCEND-4 中当前吸烟者比例更高(8.0% vs 4.4%),年龄小于 65 岁的患者比例更低(78.5% vs 84.0%)。匹配后,这两个试验人群的所有其他患者特征均平衡。与克唑替尼相比,塞瑞替尼的 PFS 显著延长(风险比[95%置信区间](HR[CI])=0.64[0.47-0.87];中位 PFS:25.2 与 10.8 个月,对数秩检验值=0.003)。OS 无显著差异,塞瑞替尼的 HR 为 0.82[0.54-1.27],与克唑替尼相比。在与外部对照的调整后间接比较中,第二代抑制剂塞瑞替尼作为一线治疗 ALK 阳性 NSCLC,与克唑替尼相比,PFS 显著延长。

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