ALK and NSCLC: Targeted therapy with ALK inhibitors.

F1000 medicine reports Pub Date : 2011-01-01 Epub Date: 2011-11-01 DOI:10.3410/M3-21
Bengt Hallberg, Ruth H Palmer
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Abstract

For many years treatment for advanced or metastatic non-small cell lung cancer (NSCLC) has employed chemotherapy regimens for patient care, with limited effect. Five-year survival rates for these patients are not encouraging. However, for a subgroup of these patients, there have been radical changes over recent years. Our understanding of the basic pathology behind NSCLC at the molecular level has offered up a host of new molecularly targeted therapies, which are revolutionizing this area of cancer care. Results from recent clinical trials provide hope for NSCLC patients harboring oncogenic translocations involving the anaplastic lymphoma kinase (ALK) receptor tyrosine kinase. Just as inhibition of the breakpoint cluster region-ABL complex has changed the face of chronic myeloid leukemia diagnosis, oncogenic ALK fusions offer a step forward in the diagnosis and treatment of ALK-positive NSCLC. This article discusses the current knowledge and potential implications concerning ALK inhibitors and NSCLC.

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ALK 和 NSCLC:ALK 抑制剂的靶向治疗。
多年来,晚期或转移性非小细胞肺癌(NSCLC)的治疗一直采用化疗方案,但效果有限。这些患者的五年生存率并不乐观。然而,对于这些患者中的一个亚群来说,近年来发生了翻天覆地的变化。我们在分子水平上对 NSCLC 的基本病理有了更深入的了解,这为我们提供了大量新的分子靶向疗法,从而彻底改变了这一癌症治疗领域。最近的临床试验结果为携带无性淋巴瘤激酶(ALK)受体酪氨酸激酶致癌易位的 NSCLC 患者带来了希望。正如抑制断点簇区-ABL复合物改变了慢性粒细胞白血病诊断的面貌一样,致癌ALK融合也为ALK阳性NSCLC的诊断和治疗提供了前进的一步。本文讨论了有关 ALK 抑制剂和 NSCLC 的现有知识和潜在影响。
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