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PROFILE 1029 研究结果:ALK 阳性晚期非小细胞肺癌一线克唑替尼对比化疗在东亚患者中的疗效比较。

Results of PROFILE 1029, a Phase III Comparison of First-Line Crizotinib versus Chemotherapy in East Asian Patients with ALK-Positive Advanced Non-Small Cell Lung Cancer.

机构信息

Guangdong Lung Cancer Institute, Guangdong General Hospital and Guangdong Academy of Medical Sciences, Guangzhou, People's Republic of China.

Department of Shanghai Lung Cancer Center, Shanghai Chest Hospital, Jiao Tong University, Shanghai, People's Republic of China.

出版信息

J Thorac Oncol. 2018 Oct;13(10):1539-1548. doi: 10.1016/j.jtho.2018.06.012. Epub 2018 Aug 14.

Abstract

INTRODUCTION

The phase III randomized PROFILE 1014 study demonstrated superiority of crizotinib to first-line chemotherapy in prolonging progression-free survival (PFS) in previously untreated patients with ALK receptor tyrosine kinase gene (ALK)-positive advanced nonsquamous NSCLC. This result was consistent with that in the smaller subset of East Asian patients in PROFILE 1014. The subsequent study reported here prospectively evaluated crizotinib in a larger East Asian patient population.

METHODS

In this open-label phase III study (PROFILE 1029), patients were randomized 1:1 to receive orally administered crizotinib 250 mg twice daily continuously (3-week cycles) or intravenously administered chemotherapy (pemetrexed 500 mg/m, plus cisplatin 75 mg/m, or carboplatin [at a dose to produce area under the concentration-time curve of 5-6 mg·min/mL]) every 3 weeks for a maximum of six cycles. PFS confirmed by independent radiology review was the primary end point.

RESULTS

Crizotinib significantly prolonged PFS (hazard ratio, 0.402; 95% confidence interval [CI]: 0.286-0.565; p < 0.001). The median PFS was 11.1 months with crizotinib and 6.8 months with chemotherapy. The objective response rate was 87.5% (95% CI: 79.6-93.2%) with crizotinib versus 45.6% (95% CI: 35.8-55.7%) with chemotherapy (p < 0.001). The most common adverse events were increased transaminase levels, diarrhea, and vision disorders with crizotinib and leukopenia, neutropenia, and anemia with chemotherapy. Significantly greater improvements from baseline in patient-reported outcomes were seen in crizotinib-treated versus chemotherapy-treated patients.

CONCLUSIONS

First-line crizotinib significantly improved PFS, objective response rate, and patient-reported outcomes compared with standard platinum-based chemotherapy in East Asian patients with ALK-positive advanced NSCLC, which is similar to the results from PROFILE 1014. The safety profiles of crizotinib and chemotherapy were consistent with those previously published.

摘要

介绍

III 期随机 PROFILE 1014 研究表明,与一线化疗相比,克唑替尼可显著延长初治ALK 受体酪氨酸激酶基因(ALK)阳性晚期非鳞状 NSCLC 患者的无进展生存期(PFS)。这一结果与 PROFILE 1014 中东亚亚组较小的患者群体一致。随后的这项前瞻性研究报告了在更大的东亚患者群体中评估克唑替尼的结果。

方法

在这项开放标签的 III 期研究(PROFILE 1029)中,患者按 1:1 随机接受口服克唑替尼 250mg,每日 2 次(3 周周期)或静脉内给予培美曲塞 500mg/m2,顺铂 75mg/m2,或卡铂(剂量使浓度-时间曲线下面积达到 5-6mg·min/mL),每 3 周一次,最多 6 个周期。独立放射学审查确认的 PFS 是主要终点。

结果

克唑替尼显著延长了 PFS(风险比,0.402;95%置信区间[CI]:0.286-0.565;p<0.001)。克唑替尼组的中位 PFS 为 11.1 个月,化疗组为 6.8 个月。克唑替尼组的客观缓解率为 87.5%(95%CI:79.6-93.2%),化疗组为 45.6%(95%CI:35.8-55.7%)(p<0.001)。克唑替尼组最常见的不良反应为肝转氨酶升高、腹泻和视力障碍,化疗组为白细胞减少、中性粒细胞减少和贫血。与化疗组相比,克唑替尼组患者报告的结局有显著改善。

结论

与标准铂类化疗相比,一线克唑替尼显著改善了东亚 ALK 阳性晚期 NSCLC 患者的 PFS、客观缓解率和患者报告的结局,这与 PROFILE 1014 的结果相似。克唑替尼和化疗的安全性与先前发表的结果一致。

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