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Durvalumab after Chemoradiotherapy in Stage III Non-Small-Cell Lung Cancer.Durvalumab 用于 III 期非小细胞肺癌放化疗后的治疗。
N Engl J Med. 2017 Nov 16;377(20):1919-1929. doi: 10.1056/NEJMoa1709937. Epub 2017 Sep 8.
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Neoadjuvant Chemoradiotherapy vesus Chemotherapy alone Followed by Surgery for Resectable Stage III Non-Small-Cell Lung Cancer: a Meta-Analysis.新辅助放化疗与单纯化疗后手术治疗可切除的Ⅲ期非小细胞肺癌的Meta分析
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Outcome after PORT in ypN2 or R1/R2 versus no PORT in ypN0 Stage III-N2 NSCLC after Induction Chemotherapy and Resection.诱导化疗和切除术治疗后 ypN0 期 III-N2 NSCLC 患者中 PORT(胸内淋巴结放疗)在 ypN2 或 R1/R2 患者与无 PORT 患者的预后比较。
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Institutional Enrollment and Survival Among NSCLC Patients Receiving Chemoradiation: NRG Oncology Radiation Therapy Oncology Group (RTOG) 0617.接受放化疗的非小细胞肺癌患者的机构登记与生存情况:NRG肿瘤学放射治疗肿瘤学组(RTOG)0617研究
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Management of stage IIIA (N2) non-small cell lung cancer: A transatlantic perspective.ⅢA期(N2)非小细胞肺癌的治疗:跨大西洋视角
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Induction chemoradiation in stage IIIA/N2 non-small-cell lung cancer: a phase 3 randomised trial.诱导化疗联合放化疗治疗 IIIA/N2 期非小细胞肺癌:一项 3 期随机试验。
Lancet. 2015 Sep 12;386(9998):1049-56. doi: 10.1016/S0140-6736(15)60294-X. Epub 2015 Aug 11.
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Adding radiation to induction chemotherapy does not improve survival of patients with operable clinical N2 non-small cell lung cancer.在诱导化疗基础上加用放疗并不能提高可手术切除的临床N2期非小细胞肺癌患者的生存率。
J Thorac Cardiovasc Surg. 2015 Dec;150(6):1484-92; discussion 1492-3. doi: 10.1016/j.jtcvs.2015.06.062. Epub 2015 Jul 2.
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A phase 3 study of induction treatment with concurrent chemoradiotherapy versus chemotherapy before surgery in patients with pathologically confirmed N2 stage IIIA nonsmall cell lung cancer (WJTOG9903).一项针对病理确诊的 N2 期 IIIA 期非小细胞肺癌患者,在手术前采用同期放化疗与化疗进行诱导治疗的 3 期研究(WJTOG9903)。
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Radiotherapy plus chemotherapy with or without surgical resection for stage III non-small-cell lung cancer: a phase III randomised controlled trial.III期非小细胞肺癌的放疗联合化疗(无论是否进行手术切除):一项III期随机对照试验
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多模态治疗 N2 期非小细胞肺癌:一个不断发展的范例。

Multimodality Therapy for N2 Non-Small Cell Lung Cancer: An Evolving Paradigm.

机构信息

Division of Thoracic Surgery, McGill University Health Centre, Montréal, Quebec, Canada.

Department of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas; Department of Epidemiology, Human Genetics and Environmental Sciences, The University of Texas Health Science Center (UTHealth) School of Public Health, Houston, Texas.

出版信息

Ann Thorac Surg. 2019 Jan;107(1):277-284. doi: 10.1016/j.athoracsur.2018.07.033. Epub 2018 Sep 15.

DOI:10.1016/j.athoracsur.2018.07.033
PMID:30227129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6993842/
Abstract

BACKGROUND

Induction chemoradiation for resectable N2 non-small cell lung cancer (NSCLC) is used with the intent to optimize locoregional control, whereas induction chemotherapy given in systemic doses is meant to optimally target potential distant disease. However, the optimal preoperative treatment regimen is still unknown and practice patterns continue to vary widely. We compared multiinstitutional oncologic outcomes for N2 NSCLC from 4 experienced lung cancer treatment centers.

METHODS

This collaborative retrospective study unites 4 major thoracic oncology centers. Patients with N2 NSCLC undergoing surgical resection after induction chemotherapy (CxT) or concurrent chemoradiation (CxRT) were included. Primary outcomes were overall and disease-free survival (OS and DFS).

RESULTS

822 patients were identified (CxT = 662 and CxRT = 160). There were no differences in 5-year OS (CxT 39.9% versus CxRT 42.9%, p = 0.250) nor in DFS (CxT 28.7% versus 29.8%, p = 0.207). Recurrence rates (CxT 46.8% versus CxRT 51.6%, p = 0.282) and recurrence patterns were not significantly different (Local: CxT 9.8% versus CxRT 9.7%; and Distant: CxT 30.4% versus CxRT 33.1%, p = 0.764). There was no difference in perioperative mortality. In the analyses of patients who underwent pretreatment invasive mediastinal staging (n = 555), there were still no significant differences in OS (p = 0.341) and DFS (p = 0.455) between the 2 treatment strategies.

CONCLUSIONS

Both treatment strategies produce equivalent and better than expected outcomes compared with historical controls for N2 NSCLC, with no differences in recurrence patterns. How these conventional therapeutic strategies will compare with those involving immunotherapy combined with surgical locoregional disease control for N2 disease remains to be determined.

摘要

背景

可切除 N2 非小细胞肺癌(NSCLC)采用诱导放化疗旨在优化局部区域控制,而全身剂量给予诱导化疗旨在最佳靶向潜在远处疾病。然而,最佳术前治疗方案仍不清楚,且实践模式仍存在很大差异。我们比较了 4 个经验丰富的肺癌治疗中心的 N2 NSCLC 的多机构肿瘤学结果。

方法

这项合作回顾性研究联合了 4 个主要的胸科肿瘤中心。纳入接受诱导化疗(CxT)或同步放化疗(CxRT)后行手术切除的 N2 NSCLC 患者。主要结局是总生存(OS)和无病生存(DFS)。

结果

共纳入 822 例患者(CxT 662 例,CxRT 160 例)。5 年 OS 无差异(CxT 39.9% vs CxRT 42.9%,p=0.250),DFS 也无差异(CxT 28.7% vs CxRT 29.8%,p=0.207)。复发率(CxT 46.8% vs CxRT 51.6%,p=0.282)和复发模式无显著差异(局部:CxT 9.8% vs CxRT 9.7%;远处:CxT 30.4% vs CxRT 33.1%,p=0.764)。围手术期死亡率无差异。在对行术前侵袭性纵隔分期的患者(n=555)进行分析时,2 种治疗策略在 OS(p=0.341)和 DFS(p=0.455)方面仍无显著差异。

结论

与 N2 NSCLC 的历史对照相比,这两种治疗策略都产生了等效甚至更好的结果,且复发模式无差异。这些传统治疗策略与将免疫治疗与手术局部区域疾病控制相结合用于 N2 疾病的策略相比如何,还有待确定。