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实现可切除非小细胞肺癌最佳病理分期。

Towards optimal pathologic staging of resectable non-small cell lung cancer.

机构信息

Thoracic Oncology Research Group, Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN, USA ;

Toronto General Hospital, University Health Network, University of Toronto, Toronto, Canada.

出版信息

Transl Lung Cancer Res. 2013 Oct;2(5):364-71. doi: 10.3978/j.issn.2218-6751.2013.10.04.

Abstract

Pathologic nodal staging is the most accurate means of determining prognosis of patients with resectable non-small cell lung cancer (NSCLC), but confusion prevails about the optimal pre-operative and surgical lymph node examination procedures for candidates of curative-intent resection. The landmark American College of Surgeons Oncology Group Z0030 trial revealed no difference in the survival of patients with clinical T1 or T2, N0 or N1 (hilar node-negative), M0 NSCLC who either had a fastidious, pre-defined systematic hilar and mediastinal lymph node sampling procedure, or who received a complete mediastinal lymph node dissection. We place the results of this major trial into a contemporary clinical practice context, and discuss problems associated with apparent misunderstanding of the lessons from this trial, especially in light of evidence of prevailing sub-optimal nodal examination practices. We also discuss evolving knowledge about the origin of the quality gap in pathologic nodal staging and the emerging literature on corrective interventions.

摘要

病理淋巴结分期是确定可切除非小细胞肺癌(NSCLC)患者预后的最准确手段,但对于有治愈性切除意向的患者,最佳术前和手术淋巴结检查程序仍存在混淆。具有里程碑意义的美国外科医师学院肿瘤学组 Z0030 试验表明,临床 T1 或 T2、N0 或 N1(肺门淋巴结阴性)、M0 NSCLC 患者的生存率无差异,这些患者要么接受了严格的、预先定义的系统肺门和纵隔淋巴结取样程序,要么接受了完全纵隔淋巴结清扫。我们将这一主要试验的结果置于当代临床实践背景下,并讨论了与明显误解该试验结果相关的问题,特别是考虑到证据表明存在淋巴结检查实践不佳的情况。我们还讨论了关于病理淋巴结分期质量差距的起源和关于纠正干预措施的新文献中不断发展的知识。

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