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克唑替尼:从发现到加速开发再到一线治疗。

Crizotinib: from discovery to accelerated development to front-line treatment.

机构信息

Christie NHS Foundation Trust, Institute of Cancer Sciences, University of Manchester, Manchester, UK

Department of Oncology, AUSL della Romagna, Ravenna, Italy.

出版信息

Ann Oncol. 2016 Sep;27 Suppl 3:iii35-iii41. doi: 10.1093/annonc/mdw304.

Abstract

Non-small-cell lung cancer (NSCLC) is associated with a poor prognosis and low survival rates, providing a strong rationale for the development of new treatment options. The discovery of ALK gene rearrangements in a subset of NSCLC specimens and the identification and development of the first-in-class ALK inhibitor crizotinib provided a personalised treatment option for patients with advanced ALK-positive NSCLC. Crizotinib demonstrated rapid and durable responses in advanced ALK-positive NSCLC patients in phase I and II studies, leading to accelerated FDA approval. Subsequent evaluation in phase III studies showed that crizotinib improved progression-free survival compared with platinum-based doublet chemotherapy in previously untreated patients and compared with pemetrexed or docetaxel in previously treated patients. Crizotinib was shown to have an acceptable safety profile and also to improve quality of life and symptom scores. Overall, crizotinib has been shown to provide a valuable first- and second-line treatment option and is now the first-line standard of care for patients with advanced ALK-positive NSCLC.

摘要

非小细胞肺癌(NSCLC)预后不良,生存率低,这为开发新的治疗方案提供了强有力的依据。在一部分 NSCLC 标本中发现了 ALK 基因重排,以及发现并开发了第一代 ALK 抑制剂克唑替尼,为晚期 ALK 阳性 NSCLC 患者提供了一种个体化的治疗选择。在 I 期和 II 期研究中,克唑替尼在晚期 ALK 阳性 NSCLC 患者中表现出快速和持久的反应,促使 FDA 加速批准。随后在 III 期研究中的评估表明,与顺铂类双药化疗相比,克唑替尼在未经治疗的患者中改善了无进展生存期,与培美曲塞或多西他赛相比,在经治患者中也改善了无进展生存期。克唑替尼的安全性特征可接受,还改善了生活质量和症状评分。总的来说,克唑替尼已被证明是一种有价值的一线和二线治疗选择,现在是晚期 ALK 阳性 NSCLC 患者的一线治疗标准。

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