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ALK 阳性非小细胞肺癌患者接受布加替尼早期准入项目治疗的实际治疗持续时间。

Real-world treatment duration in ALK-positive non-small-cell lung cancer patients receiving brigatinib through the early access program.

机构信息

Millennium Pharmaceuticals, Inc., Cambridge, MA 02139, USA.

EMD Serono, Inc., Billerica, MA 01821, USA.

出版信息

Future Oncol. 2020 May;16(15):1031-1041. doi: 10.2217/fon-2019-0849. Epub 2020 Apr 27.

Abstract

To assess time-to-treatment discontinuation (TTD) of brigatinib following treatment with ALK tyrosine kinase inhibitor(s) (TKIs) in patients with ALK-positive (ALK+) non-small-cell lung cancer (NSCLC) receiving brigatinib through the international early access program. Analysis was performed for patients with ALK+ NSCLC treated with prior ALK TKIs, including next-generation ALK TKIs. Data for 604 patients (21 countries), including patients with prior next-generation ALK TKIs, were reported. The median TTD of brigatinib in patients with prior crizotinib, alectinib, ceritinib or lorlatinib was 10.0, 8.7, 10.3 and 7.5 months, respectively. Brigatinib appears to be effective and tolerable in real-world clinical practice regardless of prior treatment with first or NG ALK TKIs.

摘要

评估接受 brigatinib 国际早期准入项目治疗的 ALK 阳性(ALK+)非小细胞肺癌(NSCLC)患者在先前接受 ALK 酪氨酸激酶抑制剂(TKI)治疗后的治疗终止时间(TTD)。分析了先前接受过 ALK TKI 治疗的 ALK+NSCLC 患者,包括下一代 ALK TKI。报告了 604 名患者(21 个国家)的数据,包括先前接受过下一代 ALK TKI 治疗的患者。先前接受克唑替尼、阿来替尼、塞瑞替尼或劳拉替尼治疗的患者的 brigatinib 中位 TTD 分别为 10.0、8.7、10.3 和 7.5 个月。无论先前是否接受过第一代或新一代 ALK TKI 治疗,brigatinib 在真实世界临床实践中似乎都是有效且耐受良好的。

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