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Pembrolizumab in the treatment of metastatic non-small cell lungcancer: a review of current evidence

机译:派姆单抗治疗转移性非小细胞肺癌癌症:当前证据的回顾

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摘要

Immune checkpoint inhibitors (ICPIs) are considered one of the most important breakthroughs in cancer treatment of the past decade; notably, different studies of programmed cell death protein 1 (PD-1) and programmed death-ligand 1 (PD-L1) inhibitors have reported impressive clinical activity and durable responses in patients with advanced non-small cell lung cancer (NSCLC). These findings have led to the changing of the current therapeutic algorithm of advanced NSCLC, adding a new standard first-line treatment option for patients with PD-L1-positive tumors. Pembrolizumab, a highly selective anti-PD-1 humanized monoclonal antibody, was approved by the United States Food and Drug Administration (US FDA) in October 2016 for previously untreated metastatic NSCLC patients whose tumors have high PD-L1 expression, tumor proportion score (TPS) ⩾ 50%, as well as for metastatic NSCLC patients whose tumors express PD-L1 with TPS ⩾ 1% progressing on or after platinum-based chemotherapy. However, many issues remain outstanding, mainly regarding the identification of an optimal biomarker which can help selecting patients more likely to respond to ICPIs. In this review, we discuss the clinical results obtained so far with the anti-PD-1 pembrolizumab in advanced NSCLC, commenting on the role of PD-L1 as a predictivefactor and providing an update of the future perspectives.
机译:免疫检查点抑制剂(ICPIs)被认为是过去十年来癌症治疗中最重要的突破之一。值得注意的是,对程序性细胞死亡蛋白1(PD-1)和程序性死亡配体1(PD-L1)抑制剂的不同研究已经报道了晚期非小细胞肺癌(NSCLC)患者令人印象深刻的临床活性和持久反应。这些发现导致了当前晚期NSCLC的治疗算法的改变,为PD-L1阳性肿瘤患者增加了新的标准一线治疗选择。 Pembrolizumab是一种高度选择性的抗PD-1人源化单克隆抗体,已于2016年10月获得美国食品药品监督管理局(US FDA)批准,用于肿瘤未经治疗的转移性NSCLC患者,其肿瘤中PD-L1表达高,肿瘤比例评分( (TPS)≥50%,以及转移性NSCLC患者在铂类化疗中或治疗后肿瘤进展为PD-L1,TPS≥1%。但是,许多问题仍然悬而未决,主要是在确定最佳生物标志物方面,这可以帮助选择更可能对ICPI做出反应的患者。在这篇综述中,我们讨论了迄今为止抗PD-1 pembrolizumab在晚期NSCLC中获得的临床结果,并评论了PD-L1作为一种预测性药物的作用。因素并提供对未来观点的更新。

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