Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.
Drugs. 2020 Oct;80(15):1587-1594. doi: 10.1007/s40265-020-01398-6.
Atezolizumab (Tecentriq), a fully humanized, monoclonal anti-programmed cell death ligand-1 (PD-L1) antibody, is the first immune checkpoint inhibitor to be approved, in combination with carboplatin and etoposide, for the treatment of adult patients with extensive-stage small cell lung cancer (ES-SCLC). Approval was based on primary data from the multinational phase I/III IMpower133 trial in PD-L1-unselected patients with previously untreated ES-SCLC. In this trial, induction therapy with atezolizumab plus carboplatin and etoposide followed by maintenance therapy with atezolizumab alone significantly prolonged overall survival (OS) and progression-free survival (PFS) compared with carboplatin and etoposide alone. The addition of atezolizumab to chemotherapy was generally well tolerated, with no new safety signals being identified beyond those previously reported for the individual agents. The most common grade 3-4 treatment-related adverse events with this regimen were haematological; the most common immune-related adverse events included rash and hypothyroidism. Importantly, the addition of atezolizumab to chemotherapy improved survival outcomes without adversely impacting patient-reported health-related quality of life (HRQOL). Thus, atezolizumab in combination with carboplatin plus etoposide has emerged as a valuable option for the first-line treatment of ES-SCLC and is being accepted as a standard of care in this setting.
阿替利珠单抗(Tecentriq)是一种完全人源化的、单克隆抗程序性死亡配体-1(PD-L1)抗体,是首个被批准的免疫检查点抑制剂,与卡铂和依托泊苷联合用于治疗未经治疗的广泛期小细胞肺癌(ES-SCLC)的成年患者。批准基于在 PD-L1 未选择的未经治疗的 ES-SCLC 患者中进行的多中心 I/III 期 IMpower133 试验的主要数据。在这项试验中,阿替利珠单抗联合卡铂和依托泊苷诱导治疗,然后单独用阿替利珠单抗维持治疗,与单独用卡铂和依托泊苷相比,显著延长了总生存期(OS)和无进展生存期(PFS)。与单独使用卡铂和依托泊苷相比,阿替利珠单抗联合化疗通常耐受性良好,除了先前报告的个别药物的新安全性信号外,没有发现新的安全性信号。该方案最常见的 3-4 级与治疗相关的不良事件是血液学方面的;最常见的免疫相关不良事件包括皮疹和甲状腺功能减退。重要的是,阿替利珠单抗联合化疗改善了生存结果,而没有对患者报告的健康相关生活质量(HRQOL)产生不利影响。因此,阿替利珠单抗联合卡铂加依托泊苷已成为治疗 ES-SCLC 的一线治疗的有价值的选择,并在该治疗中被接受为标准治疗。