A Practical Review of Encorafenib and Binimetinib Therapy Management in Patients with BRAF V600E-Mutant Metastatic Non-Small Cell Lung Cancer

被引:0
|
作者
Baik, Christina [1 ,2 ]
Cheng, Michael L. [3 ]
Dietrich, Martin [4 ,5 ]
Gray, Jhanelle E. [6 ]
Karim, Nagla A. [7 ]
机构
[1] Univ Washington, Seattle, WA USA
[2] Fred Hutchinson Canc Ctr, Seattle, WA USA
[3] Univ Calif San Francisco, San Francisco, CA USA
[4] US Oncol, Orlando, FL USA
[5] Univ Cent Florida, Orlando, FL USA
[6] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[7] Univ Virginia, Inova Schar Canc Inst, 8081 Innovat Pk Dr, Fairfax, VA 22031 USA
关键词
Adverse reaction management; Binimetinib; BRAF; Encorafenib; Non-small cell lung cancer; DABRAFENIB PLUS TRAMETINIB; OPEN-LABEL; MUTATIONS; MULTICENTER; INHIBITOR; NSCLC;
D O I
10.1007/s12325-024-02839-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
According to current guidelines, targeted therapy with a combination of BRAF plus MEK inhibitors is the preferred first-line treatment for patients with BRAF V600E-mutant metastatic non-small cell lung cancer (NSCLC). In the open-label, single-arm, phase 2 PHAROS trial (NCT03915951), the combination of encorafenib, a potent BRAF inhibitor, and binimetinib, a potent MEK inhibitor, demonstrated durable antitumor activity with a manageable safety profile in this patient population. On the basis of the results of this study, the combination of encorafenib plus binimetinib was approved by the US Food and Drug Administration on October 11, 2023, for patients with BRAF V600E-mutant metastatic NSCLC. In this review, we summarize the efficacy and safety of encorafenib plus binimetinib from the PHAROS study. In addition, we discuss strategies to manage adverse reactions with this combination therapy with the intent of minimizing unnecessary treatment discontinuations in these patients.
引用
收藏
页码:2586 / 2605
页数:20
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