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Overall Survival and Biomarker Analysis of Neoadjuvant Nivolumab Plus Chemotherapy in Operable Stage IIIA Non-Small-Cell Lung Cancer (NADIM phase II trial).新辅助纳武利尤单抗联合化疗治疗可手术 IIIA 期非小细胞肺癌的总生存和生物标志物分析(NADIM Ⅱ期试验)。
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Neoadjuvant Nivolumab plus Chemotherapy in Resectable Lung Cancer.新辅助纳武利尤单抗联合化疗治疗可切除肺癌。
N Engl J Med. 2022 May 26;386(21):1973-1985. doi: 10.1056/NEJMoa2202170. Epub 2022 Apr 11.
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Adjuvant atezolizumab after adjuvant chemotherapy in resected stage IB-IIIA non-small-cell lung cancer (IMpower010): a randomised, multicentre, open-label, phase 3 trial.辅助阿特珠单抗治疗辅助化疗后切除的 IB-IIIA 期非小细胞肺癌(IMpower010):一项随机、多中心、开放标签、III 期临床试验。
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Neoadjuvant osimertinib with/without chemotherapy versus chemotherapy alone for -mutated resectable non-small-cell lung cancer: NeoADAURA.奥希替尼新辅助治疗联合/不联合化疗对比单纯化疗用于可切除 - 突变型非小细胞肺癌:NeoADAURA 研究。
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SAKK 16/14: Durvalumab in Addition to Neoadjuvant Chemotherapy in Patients With Stage IIIA(N2) Non-Small-Cell Lung Cancer-A Multicenter Single-Arm Phase II Trial.SAKK 16/14:在 IIIA(N2)期非小细胞肺癌患者中,新辅助化疗联合度伐利尤单抗:一项多中心单臂 II 期试验。
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Neoadjuvant nivolumab or nivolumab plus ipilimumab in operable non-small cell lung cancer: the phase 2 randomized NEOSTAR trial.可切除非小细胞肺癌的新辅助纳武利尤单抗或纳武利尤单抗联合伊匹单抗:Ⅱ期随机 NEOSTAR 试验。
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Efficacy and Safety of PD-1/PD-L1 Inhibitors Plus Chemotherapy Versus PD-1/PD-L1 Inhibitors in Advanced Non-Small Cell Lung Cancer: A Network Analysis of Randomized Controlled Trials.PD-1/PD-L1抑制剂联合化疗与PD-1/PD-L1抑制剂治疗晚期非小细胞肺癌的疗效和安全性:一项随机对照试验的网状分析
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Neoadjuvant atezolizumab and chemotherapy in patients with resectable non-small-cell lung cancer: an open-label, multicentre, single-arm, phase 2 trial.可切除非小细胞肺癌患者新辅助阿替利珠单抗和化疗:一项开放标签、多中心、单臂、2 期临床试验。
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可切除非小细胞肺癌诱导治疗新时代的开端:一项叙述性综述

The beginning of a new era in induction treatment for operable non-small cell lung cancer: a narrative review.

作者信息

Shinohara Shuichi, Takahashi Yusuke, Masago Katsuhiro, Matsushita Hirokazu, Kuroda Hiroaki

机构信息

Department of Thoracic Surgery, Aichi Cancer Center Hospital, Nagoya, Japan.

Division of Oncoimmunology, Aichi Cancer Center Research Institute, Nagoya, Japan.

出版信息

J Thorac Dis. 2023 Feb 28;15(2):747-758. doi: 10.21037/jtd-22-957. Epub 2023 Feb 2.

DOI:10.21037/jtd-22-957
PMID:36910085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9992625/
Abstract

BACKGROUND AND OBJECTIVE

The survival benefit of induction therapy for non-small cell lung cancer (NSCLC) remains controversial. Recently, the outcomes of systemic therapy for NSCLC have dramatically changed with the advent of molecular target drugs and immune checkpoint inhibitors (ICIs). The present review was conducted to investigate the outcomes of induction therapy with reference to randomized control trials (RCTs).

METHODS

We reviewed RCTs and ongoing clinical trials between 1990 and 2022 using relevant databases: PubMed, Web of Science, and EMBASE database. We investigated the outcomes of induction therapy.

KEY CONTENT AND FINDINGS

Induction therapy was associated with longer overall survival in comparison to surgery alone in several RCTs for stage III disease. However, its benefit in early-stage (I-II) disease was unclear. Regarding induction chemotherapy and chemoradiotherapy, the safety and survival outcomes did not differ between the two arms. Epidermoid growth factor receptor (EGFR) tyrosine kinase inhibitors as induction therapy in patients with proven EGFR mutations may be a sufficient choice for the improvement of overall survival. In ongoing single arm clinical trials and a randomized control study, the administration of ICIs as induction therapy was associated with a good pathological response and satisfactory safety, which will lead to a better survival outcome. Long-term observation is needed to evaluate the toxicity and survival impact of induction therapy with ICIs.

CONCLUSIONS

Induction chemotherapy and EGFR-TKIs for stage IIIA NSCLC may contribute to the improvement of survival outcomes although the effect of systemic therapy on stage I-II remains controversial. ICIs may be considered as a valuable treatment option because of their feasibility and safety for induction therapy.

摘要

背景与目的

非小细胞肺癌(NSCLC)诱导治疗的生存获益仍存在争议。近年来,随着分子靶向药物和免疫检查点抑制剂(ICI)的出现,NSCLC全身治疗的结果发生了显著变化。本综述旨在参考随机对照试验(RCT)来研究诱导治疗的结果。

方法

我们使用相关数据库(PubMed、科学网和EMBASE数据库)回顾了1990年至2022年间的RCT和正在进行的临床试验。我们研究了诱导治疗的结果。

关键内容与发现

在几项针对III期疾病的RCT中,与单纯手术相比,诱导治疗与更长的总生存期相关。然而,其在早期(I-II期)疾病中的获益尚不清楚。关于诱导化疗和放化疗,两组的安全性和生存结果没有差异。对于已证实EGFR突变的患者,表皮生长因子受体(EGFR)酪氨酸激酶抑制剂作为诱导治疗可能是改善总生存期的充分选择。在正在进行的单臂临床试验和一项随机对照研究中,ICI作为诱导治疗的应用与良好的病理反应和令人满意的安全性相关,这将带来更好的生存结果。需要长期观察来评估ICI诱导治疗的毒性和生存影响。

结论

尽管全身治疗对I-II期NSCLC的疗效仍存在争议,但III期NSCLC的诱导化疗和EGFR-TKI可能有助于改善生存结果。由于ICI诱导治疗的可行性和安全性,可将其视为一种有价值的治疗选择。