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Chinese perspectives on clinical efficacy and safety of alectinib in patients with ALK-positive advanced non-small cell lung cancer

机译:中国对爱乐替尼治疗ALK阳性晚期非小细胞肺癌的临床疗效和安全性的观点

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摘要

The incidence of lung cancer is increasing in China, in contrast to trends in Western countries, due to the increasing numbers of smokers and high levels of air pollution. Non-small-cell lung cancer (NSCLC) is the most common form of lung cancer, accounting for approximately 85% of lung cancers. Better understanding of the pathogenesis of NSCLC has led to the identification of multiple genetic mutations and chromosomal translocations such as those in the anaplastic lymphoma kinase (ALK) gene. To facilitate the identification of treatment targets, multiple guidelines (European Society for Medical Oncology, National Comprehensive Cancer Network, and American Society of Clinical Oncology) now recommend screening for genetic factors to help guide treatment decisions. In recent years, multiple ALK inhibitors have been developed to treat NSCLC, including the first-generation tyrosine kinase inhibitor (TKI) crizotinib; second-generation TKIs such as ceritinib, ensartinib, brigatinib, and alectinib; the third-generation TKI lorlatinib; and the fourth-generation TKI repotrectinib. These agents differ in structure, potency, and activity, both systemically and their effects on central nervous system (CNS) metastases. Recently, alectinib was approved in China to treat patients with locally advanced or metastatic NSCLC that were ALK+. Alectinib has demonstrated activity against NSCLC, including metastases within the CNS, with better tolerability than crizotinib. These ALK inhibitors represent significant advances in the treatment of NSCLC and yet patients will likely still exhibit disease progression. Alectinib offers greater potency with greater specificity as well as a better toxicity profile than many other TKIs that are currently available. Here, we review the role of ALK as a therapeutic target in NSCLC, the testing methods for identifying ALK-rearranged NSCLC, and the various TKIs currently being used or explored for treatment in this setting, with a focus on alectinib from a Chinese perspective.
机译:与西方国家的趋势相反,中国的肺癌发病率正在增加,这是由于吸烟者数量增加和空气污染水平高。非小细胞肺癌(NSCLC)是最常见的肺癌形式,约占肺癌总数的85%。对NSCLC发病机理的更好理解已导致鉴定出多种基因突变和染色体易位,例如间变性淋巴瘤激酶(ALK)基因中的突变。为了帮助确定治疗目标,现在建议使用多个指南(欧洲医学肿瘤学会,国家综合癌症网络和美国临床肿瘤学会)筛查遗传因素,以帮助指导治疗决策。近年来,已经开发出多种ALK抑制剂来治疗NSCLC,包括第一代酪氨酸激酶抑制剂(TKI)crizotinib;第二代TKI,例如ceritinib,ensartinib,brigatinib和alectinib;第三代TKI洛莱替尼;和第四代TKI repotrectinib。这些药物在结构上,效力和活性上均在系统方面不同,并且它们对中枢神经系统(CNS)转移的影响也不同。最近,艾乐替尼在中国被批准用于治疗ALK +局部晚期或转移性NSCLC患者。艾乐替尼已显示出抗非小细胞肺癌的活性,包括中枢神经系统内的转移,其耐受性比克唑替尼更好。这些ALK抑制剂代表了NSCLC治疗的重大进展,但患者仍可能会出现疾病进展。与目前可用的许多其他TKI相比,Alectinib具有更高的效价,更高的特异性和更高的毒性。在这里,我们回顾了ALK在NSCLC中作为治疗靶点的作用,鉴定ALK重排的NSCLC的测试方法以及在这种情况下目前正在使用或探索用于治疗的各种TKI,从中国的角度着眼于艾乐替尼。

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