Marchiò Caterina, Gatti Gaia, Massa Federica, Bertero Luca, Filosso Pierluigi, Pelosi Giuseppe, Cassoni Paola, Volante Marco, Papotti Mauro
Department of Medical Sciences, University of Turin, Via Giuseppe Verdi, 8, 10124, Turin, Italy.
Pathology Division, AOU Città della Salute e della Scienza di Torino, Via Santena 7, 10126, Turin, Italy.
Virchows Arch. 2017 Dec;471(6):713-720. doi: 10.1007/s00428-017-2177-0. Epub 2017 Jun 19.
Typical (TCs) and atypical carcinoids (ACs) are defined based on morphological criteria, and no grading system is currently accepted to further stratify these entities. The 2015 WHO classification restricts the Ki-67 role to biopsy or cytology samples, rather than for prognostic prediction. We aimed to investigate whether values and patterns of Ki-67 alone would allow for a clinically meaningful stratification of lung carcinoids, regardless of histological typing. Ki-67 proliferation index and pattern (homogeneous versus heterogeneous expression) were assessed in a cohort of 171 TCs and 68 ACs. Cases were subdivided into three Ki-67 ranges (<4/4-9/≥10%). Correlations with clinicopathological data, univariate and multivariate survival analyses were performed. The majority of cases (61.5%) belonged to the <4% Ki-67 range; 25.1 and 13.4% had a proliferation index of 4-9% and ≥10%, respectively. The <4% Ki-67 subgroup was significantly enriched for TCs (83%, p < 0.0001); ACs were more frequent in the subgroup showing Ki-67 ≥ 10% (75%, p < 0.0001). A heterogeneous Ki-67 pattern was preferentially seen in carcinoids with a Ki-67 ≥10% (38%, p < 0.02). Mean Ki-67 values ≥4 and ≥10% identified categories of poor prognosis both in terms of disease-free and overall survival (p = 0.003 and <0.0001). At multivariate analysis, the two thresholds did not retain statistical significance; however, a Ki-67 ≥ 10% identified a subgroup of dismal prognosis even within ACs (p = 0.03) at univariate analysis. Here, we describe a subgroup of lung carcinoids showing brisk proliferation activity within the necrosis and/or mitotic count-based categories. These patients were associated with specific clinicopathological characteristics, to some extent regardless of histological subtyping.
典型类癌(TCs)和非典型类癌(ACs)是根据形态学标准定义的,目前尚无被广泛接受的分级系统来进一步区分这些实体。2015年世界卫生组织(WHO)分类将Ki-67的作用限制在活检或细胞学样本中,而非用于预后预测。我们旨在研究仅通过Ki-67的值和模式是否能对肺类癌进行具有临床意义的分层,而不考虑组织学类型。我们对171例TCs和68例ACs队列中的Ki-67增殖指数和模式(均匀表达与异质性表达)进行了评估。病例被分为三个Ki-67范围(<4%/4%-9%/≥10%)。进行了与临床病理数据的相关性分析、单因素和多因素生存分析。大多数病例(61.5%)属于Ki-67<4%的范围;25.1%和13.4%的增殖指数分别为4%-9%和≥10%。Ki-67<4%的亚组中TCs显著富集(83%,p<0.0001);在Ki-67≥10%的亚组中ACs更为常见(75%,p<0.0001)。异质性Ki-67模式在Ki-67≥10%的类癌中更为常见(38%,p<0.02)。平均Ki-67值≥4%和≥10%在无病生存期和总生存期方面均确定了预后不良的类别(p=0.003和<0.0001)。在多因素分析中,这两个阈值没有统计学意义;然而,在单因素分析中,Ki-67≥10%即使在ACs中也确定了一个预后不良的亚组(p=0.03)。在此,我们描述了一组肺类癌,其在基于坏死和/或有丝分裂计数的类别中显示出活跃的增殖活性。这些患者具有特定的临床病理特征,在一定程度上与组织学亚型无关。