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明智选择非小细胞肺癌(NSCLC)一线免疫治疗:该加什么,该弃什么。

Choosing wisely first line immunotherapy in non-small cell lung cancer (NSCLC): what to add and what to leave out.

机构信息

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

出版信息

Cancer Treat Rev. 2019 May;75:39-51. doi: 10.1016/j.ctrv.2019.03.004. Epub 2019 Mar 28.

Abstract

Immunotherapy has dramatically changed the therapeutic scenario in treatment naïve advanced non-small cell lung cancer (NSCLC). While single agent pembrolizumab has become the standard therapy in patients with PD-L1 expression on tumor cells ≥ 50%, the combination of pembrolizumab or atezolizumab and platinum-based chemotherapy has emerged as an effective first line treatment regardless of PD-L1 expression both in squamous and non-squamous NSCLC without oncogenic drivers. Furthermore, double immune checkpoint inhibition has shown promising results in treatment naïve patients with high tumor mutational burden (TMB). Of note, the presence of both negative PD-L1 expression and low TMB may identify a subgroup of patients who has little benefit from immunotherapy combinations and for whom the best treatment option may still be platinum-based chemotherapy. To date, first-line single agent immune checkpoint blockade has demonstrated limited activity in EGFR mutated NSCLC and the combination of immunotherapy and targeted agents has raised safety concerns in both EGFR and ALK positive NSCLC patients. Finally, in EGFR mutated or ALK rearranged NSCLC, atezolizumab in combination with platinum-based chemotherapy and bevacizumab is emerging as a potential treatment option upon progression to first line tyrosine kinase inhibitors.

摘要

免疫疗法极大地改变了未经治疗的晚期非小细胞肺癌(NSCLC)的治疗格局。虽然在肿瘤细胞 PD-L1 表达≥50%的患者中,单药 pembrolizumab 已成为标准治疗,但 pembrolizumab 或 atezolizumab 联合铂类化疗无论 PD-L1 表达如何,已成为鳞状和非鳞状 NSCLC 中无致癌驱动基因的有效一线治疗方法。此外,双免疫检查点抑制在高肿瘤突变负荷(TMB)的初治患者中显示出有希望的结果。值得注意的是,阴性 PD-L1 表达和低 TMB 均存在可能确定一组患者从免疫治疗联合治疗中获益甚少,而铂类化疗可能仍然是最佳治疗选择。迄今为止,一线单药免疫检查点阻断在 EGFR 突变型 NSCLC 中的活性有限,免疫治疗与靶向药物联合应用在 EGFR 和 ALK 阳性 NSCLC 患者中引起了安全性问题。最后,在 EGFR 突变或 ALK 重排的 NSCLC 中,在进展为一线酪氨酸激酶抑制剂时,atezolizumab 联合铂类化疗和贝伐珠单抗可能成为一种潜在的治疗选择。

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