Royal Brompton and Harefield National Health Service Foundation Trust and National Heart and Lung Institute, Imperial College, London/United Kingdom.
University of Colorado Anschutz Medical Campus, Aurora, Colorado.
J Thorac Oncol. 2018 Feb;13(2):205-217. doi: 10.1016/j.jtho.2017.10.019. Epub 2017 Nov 7.
Multiple tumor nodules are seen with increasing frequency in clinical practice. On the basis of the 2015 WHO classification of lung tumors, we assessed the reproducibility of the comprehensive histologic assessment to distinguish second primary lung cancers (SPLCs) from intrapulmonary metastases (IPMs), looking for the most distinctive histologic features. An international panel of lung pathologists reviewed a scanned sequential cohort of 126 tumors from 48 patients and recorded an agreed set of histologic features, including tumor typing and predominant pattern of adenocarcinoma, thereby opining whether the case was SPLC, IPM, or a combination thereof. Cohen κ statistics of 0.60 on overall assessment of SPLC or IPM indicated a good agreement. Likewise, there was good agreement (κ score 0.64, p < 0.0001) between WHO histologic pattern in individual cases and SPLC or IPM status, but the proportions diversified for histologic pattern and SPLC or IPM status (McNemar test, p < 0.0001). The strongest associations for distinguishing between SPLC and IPM were observed for nuclear pleomorphism, cell size, acinus formation, nucleolar size, mitotic rate, nuclear inclusions, intraalveolar clusters, and necrosis. Conversely, the associations for lymphocytosis, mucin content, lepidic growth, vascular invasion, macrophage response, clear cell change, acute inflammation keratinization, and emperipolesis did not reach significance with tumor extent. Comprehensive histologic assessment is recommended for distinguishing SPLC from IPM with good reproducibility among lung pathologists. In addition to main histologic type and predominant patterns of histologic subtypes, nuclear pleomorphism, cell size, acinus formation, nucleolar size, and mitotic rate strongly correlate with pathologic staging status.
临床上越来越多地发现多个肿瘤结节。基于 2015 年世卫组织肺癌肿瘤分类,我们评估了综合组织学评估区分第二原发肺癌(SPLC)和肺内转移(IPM)的可重复性,寻找最具特征性的组织学特征。一个国际肺癌病理学家小组回顾了来自 48 名患者的 126 个肿瘤的扫描连续队列,并记录了一组商定的组织学特征,包括肿瘤分型和腺癌的主要模式,从而判断该病例是 SPLC、IPM 还是两者的组合。总体评估 SPLC 或 IPM 的 Cohen κ 统计量为 0.60,表明存在良好的一致性。同样,在个别病例的世卫组织组织学模式与 SPLC 或 IPM 状态之间也存在良好的一致性(κ 评分 0.64,p < 0.0001),但组织学模式和 SPLC 或 IPM 状态的比例有所不同(McNemar 检验,p < 0.0001)。区分 SPLC 和 IPM 的最强关联是核多形性、细胞大小、腺泡形成、核仁大小、有丝分裂率、核内包涵体、肺泡内簇和坏死。相反,对于区分 SPLC 和 IPM,淋巴细胞增多、粘蛋白含量、贴壁生长、血管侵犯、巨噬细胞反应、透明细胞改变、急性炎症角化和吞噬现象与肿瘤程度没有相关性。推荐综合组织学评估用于区分 SPLC 和 IPM,肺病理学家之间具有良好的可重复性。除了主要组织学类型和组织学亚型的主要模式外,核多形性、细胞大小、腺泡形成、核仁大小和有丝分裂率与病理分期状态密切相关。