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免疫治疗时代广泛期小细胞肺癌的系统治疗。

Systemic Therapy of Extensive Stage Small Cell Lung Cancer in the Era of Immunotherapy.

机构信息

Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.

Department of Medicine, VA Palo Alto Health Care System, 111-ONC 3801 Miranda Avenue, Palo Alto, CA, 94304, USA.

出版信息

Curr Treat Options Oncol. 2020 Jun 29;21(8):64. doi: 10.1007/s11864-020-00762-8.

Abstract

In March 2019, the FDA approved the use of the anti-programmed death ligand 1 (PD-L1) antibody atezolizumab, as a first-line treatment option in combination with platinum-etoposide (PE) for patients with extensive stage small cell lung cancer (ED SCLC) based upon the results of the IMpower133 trial. More recently, the FDA approved the anti-PD-L1 antibody durvalumab in March 2020 , also in the frontline setting for SCLC based upon the results of the CASPIAN trial. Both these trials demonstrated a small, but significant overall survival (OS) benefit with the addition of a PD-L1 antibody to standard chemotherapy in the treatment of ED SCLC, thereby altering the treatment paradigm for this aggressive disease. Previously, the FDA had approved the anti-PD1 antibodies nivolumab and pembrolizumab as single-agent third-line treatment options based upon encouraging phase 1/2 data in patients with relapsed SCLC who had not received prior immunotherapy (IO). Despite these recent advances, the overall benefit of IO in SCLC remains somewhat disappointing in comparison with the results seen in non-small cell lung cancer (NSCLC). To date, no reliable biomarkers exist to predict responsiveness to IO in SCLC, and the utility of second- or third-line immunotherapy is questionable in patients who have received IO as part of first-line treatment. There has also been minimal success in identifying targetable mutations in SCLC. Novel approaches include combination approaches with IO, including PARP inhibitors and CDK inhibitors. Few ongoing trials, however, have enrolled patients who have received frontline immunotherapy given the only recent change in standard of care. Consequently, the results of current trials evaluating second- and third-line therapies need to be interpreted and translated into clinical practice with caution. The most significant challenge in SCLC remains the identification of molecular targets for which drugs can be developed that can improve survival over the current standard of care.

摘要

2019 年 3 月,FDA 基于 IMpower133 试验结果批准抗程序性死亡配体 1(PD-L1)抗体阿替利珠单抗与铂类依托泊苷(PE)联合用于广泛期小细胞肺癌(ED SCLC)患者的一线治疗选择。最近,FDA 基于 CASPIAN 试验结果于 2020 年 3 月批准了抗 PD-L1 抗体度伐利尤单抗用于 SCLC 的一线治疗。这两项试验都证明了在 ED SCLC 的标准化疗中添加 PD-L1 抗体可带来微小但有显著意义的总生存期(OS)获益,从而改变了这种侵袭性疾病的治疗模式。此前,FDA 已基于复发性 SCLC 患者接受免疫治疗(IO)之前的令人鼓舞的 1/2 期数据,批准了抗 PD1 抗体纳武利尤单抗和帕博利珠单抗作为单药三线治疗选择。尽管取得了这些最新进展,但与非小细胞肺癌(NSCLC)的结果相比,IO 在 SCLC 中的整体获益仍有些令人失望。迄今为止,尚无可靠的生物标志物可预测 IO 对 SCLC 的反应性,并且在作为一线治疗一部分接受 IO 的患者中,二线或三线免疫治疗的效用存在疑问。在 SCLC 中也很少有成功鉴定出可靶向的突变。新的方法包括 IO 联合治疗方法,包括 PARP 抑制剂和 CDK 抑制剂。然而,由于最近才改变了标准护理,很少有正在进行的试验招募接受过一线免疫治疗的患者。因此,需要谨慎解释和将评估二线和三线治疗的当前试验结果转化为临床实践。SCLC 面临的最大挑战仍然是确定药物可开发的分子靶点,以提高超过当前标准护理的生存率。

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