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非小细胞肺癌(NSCLC)的一线免疫检查点抑制剂治疗。

First-Line Treatment of Non-Small-Cell Lung Cancer (NSCLC) with Immune Checkpoint Inhibitors.

机构信息

Service de Pneumologie, Hôpital d'Instruction des Armées Percy, 106, avenue Henri-Barbusse, 92140, Clamart Cedex, France.

Department of Respiratory Diseases, Hôpital d'Instruction des Armées Saint-Anne, Toulon, France.

出版信息

BioDrugs. 2019 Apr;33(2):159-171. doi: 10.1007/s40259-019-00339-4.

Abstract

Treatment of advanced-stage or metastatic non-small-cell lung cancers (NSCLCs) without EGFR mutations or ALK rearrangements, which can now be treated with molecularly targeted therapies, had been based on cytotoxic chemotherapy for a long time. Immune checkpoint inhibitors (ICIs), notably antibodies directed against programmed cell-death protein-1 (PD-1) and its ligand (PD-L1) have transformed therapeutic standards in thoracic oncology. These ICIs are now the reference second-line treatment and numerous phase III trials have examined their efficacy in treatment-naïve patients. First-line pembrolizumab monotherapy was validated for patients with ≥ 50% of tumor cells expressing PD-L1; pembrolizumab, atezolizumab, and nivolumab have obtained good outcomes in combination with chemotherapy or another immunotherapy. However, in this context, other phase III trials yielded negative findings for nivolumab alone (CheckMate-026) or in combination (MYSTIC trial). Biomarkers, such as PD-L1 and the tumor mutation burden (TMB), enable better selection of patients who should benefit the most from first-line ICI use.

摘要

对于没有 EGFR 突变或 ALK 重排的晚期或转移性非小细胞肺癌(NSCLC)的治疗,现在可以采用分子靶向治疗,长期以来一直基于细胞毒性化疗。免疫检查点抑制剂(ICI),特别是针对程序性细胞死亡蛋白-1(PD-1)及其配体(PD-L1)的抗体,已经改变了胸部肿瘤学的治疗标准。这些 ICI 现在是二线治疗的参考标准,许多 III 期临床试验已经研究了它们在未经治疗的患者中的疗效。对于肿瘤细胞中 PD-L1 表达≥50%的患者,一线帕博利珠单抗单药治疗得到了验证;帕博利珠单抗、阿替利珠单抗和纳武利尤单抗与化疗或另一种免疫疗法联合使用取得了良好的效果。然而,在这种情况下,其他 III 期试验对纳武利尤单抗单药(CheckMate-026)或联合用药(MYSTIC 试验)的结果为阴性。生物标志物,如 PD-L1 和肿瘤突变负担(TMB),可以更好地选择最有可能从一线 ICI 治疗中获益的患者。

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