Literature DB >> 30670498

YH25448, an Irreversible EGFR-TKI with Potent Intracranial Activity in EGFR Mutant Non-Small Cell Lung Cancer.

Jiyeon Yun1, Min Hee Hong1,2, Hye Ryun Kim3,2, Byoung Chul Cho3,2,4, Seok-Young Kim1, Chae-Won Park1, Soyoung Kim1, Mi Ran Yun1,4, Han Na Kang1,4, Kyoung-Ho Pyo1, Sung Sook Lee5, Jong Sung Koh6, Ho-Juhn Song6, Dong Kyun Kim7, Young-Sung Lee7, Se-Woong Oh7, Soongyu Choi7.   

Abstract

PURPOSE: Given that osimertinib is the only approved third-generation EGFR-TKI against EGFR activating and resistant T790M mutated non-small cell lung cancer (NSCLC), additional mutant-selective inhibitors with a higher efficacy, especially for brain metastases, with favorable toxicity profile are still needed. In this study, we investigated the antitumor efficacy of YH25448, an oral, mutant-selective, irreversible third-generation EGFR-TKI in preclinical models. EXPERIMENTAL
DESIGN: Antitumor activity of YH25448 was investigated in vitro using mutant EGFR-expressing Ba/F3 cells and various lung cancer cell lines. In vivo antitumor efficacy, ability to penetrate the blood-brain barrier (BBB), and skin toxicity of YH25448 were examined and compared with those of osimertinib using cell lines and PDX model.
RESULTS: Compared with osimertinib, YH25448 showed a higher selectivity and potency in kinase assay and mutant EGFR-expressing Ba/F3 cells. In various cell line models harboring EGFR activating and T790M mutation, YH25448 effectively inhibited EGFR downstream signaling pathways, leading to cellular apoptosis. When compared in vivo at equimolar concentrations, YH25448 produced significantly better tumor regression than osimertinib. Importantly, YH25448 induced profound tumor regression in brain metastasis model with excellent brain/plasma and tumor/brain area under the concentration-time curve value. YH25448 rarely suppressed the levels of p-EGFR in hair follicles, leading to less keratosis than osimertinib in animal model. The potent systemic and intracranial activity of YH25448 has been shown in an ongoing phase I/II clinical trial for advanced EGFR T790M mutated NSCLC (NCT03046992).
CONCLUSIONS: Our findings suggest that YH25448 is a promising third-generation EGFR inhibitor, which may be more effective and better tolerated than the currently approved osimertinib. ©2019 American Association for Cancer Research.

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Year:  2019        PMID: 30670498     DOI: 10.1158/1078-0432.CCR-18-2906

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  11 in total

Review 1.  Third-generation epidermal growth factor receptor tyrosine kinase inhibitors for the treatment of non-small cell lung cancer.

Authors:  Natalie M Andrews Wright; Glenwood D Goss
Journal:  Transl Lung Cancer Res       Date:  2019-11

Review 2.  The optional approach of oncogene-addicted non-small cell lung cancer with brain metastases in the new generation targeted therapies era.

Authors:  Alessia Spagnuolo; Matteo Muto; Fabio Monaco; Giuseppe Colantuoni; Cesare Gridelli
Journal:  Transl Lung Cancer Res       Date:  2019-12

Review 3.  Potentiating Therapeutic Effects of Epidermal Growth Factor Receptor Inhibition in Triple-Negative Breast Cancer.

Authors:  Kyu Sic You; Yong Weon Yi; Jeonghee Cho; Jeong-Soo Park; Yeon-Sun Seong
Journal:  Pharmaceuticals (Basel)       Date:  2021-06-18

4.  Hypoxia-Mediated Complement 1q Binding Protein Regulates Metastasis and Chemoresistance in Triple-Negative Breast Cancer and Modulates the PKC-NF-κB-VCAM-1 Signaling Pathway.

Authors:  Hao Wu; Yijun Chu; Shanshan Sun; Guozheng Li; Shouping Xu; Xianyu Zhang; Yongdong Jiang; Song Gao; Qin Wang; Jian Zhang; Da Pang
Journal:  Front Cell Dev Biol       Date:  2021-02-23

5.  Prognostic impacts of extracranial metastasis on non-small cell lung cancer with brain metastasis: A retrospective study based on surveillance, epidemiology, and end results database.

Authors:  Miao Wang; Qiuji Wu; Jun Zhang; Guizhen Qin; Tian Yang; Yixin Liu; Xulong Wang; Boyu Zhang; Yongchang Wei
Journal:  Cancer Med       Date:  2020-12-15       Impact factor: 4.452

Review 6.  Mechanisms and management of 3rd‑generation EGFR‑TKI resistance in advanced non‑small cell lung cancer (Review).

Authors:  Jingyi He; Zhengrong Huang; Linzhi Han; Yan Gong; Conghua Xie
Journal:  Int J Oncol       Date:  2021-09-24       Impact factor: 5.650

7.  Cardiac Safety Assessment of Lazertinib: Findings From Patients With EGFR Mutation-Positive Advanced NSCLC and Preclinical Studies.

Authors:  Seong Bok Jang; Kyeong Bae Kim; Sujin Sim; Byoung Chul Cho; Myung-Ju Ahn; Ji-Youn Han; Sang-We Kim; Ki Hyeong Lee; Eun Kyung Cho; Nahor Haddish-Berhane; Jaydeep Mehta; Se-Woong Oh
Journal:  JTO Clin Res Rep       Date:  2021-09-08

8.  Lazertinib improves the efficacy of chemotherapeutic drugs in ABCB1 or ABCG2 overexpression cancer cells in vitro, in vivo, and ex vivo.

Authors:  Yingfang Fan; Tian Tao; Zhixing Guo; Kenneth Kin Wah To; Da Chen; Shaocong Wu; Chuan Yang; Jinsui Li; Min Luo; Fang Wang; Liwu Fu
Journal:  Mol Ther Oncolytics       Date:  2022-02-16       Impact factor: 7.200

Review 9.  Lazertinib: on the Way to Its Throne.

Authors:  Jiyun Lee; Min Hee Hong; Byoung Chul Cho
Journal:  Yonsei Med J       Date:  2022-09       Impact factor: 3.052

10.  Assessment of Effectiveness and Safety of Osimertinib for Patients With Intracranial Metastatic Disease: A Systematic Review and Meta-analysis.

Authors:  Anders W Erickson; Priscilla K Brastianos; Sunit Das
Journal:  JAMA Netw Open       Date:  2020-03-02
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