Department of Radiology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA; Department of Radiology, Hospital Sirio-Libanes, Rua Adma Jafet, 91, Sao Paulo, SP, 01308-050, Brazil.
Department of Pathology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA.
Lung Cancer. 2021 Mar;153:158-164. doi: 10.1016/j.lungcan.2021.01.019. Epub 2021 Jan 25.
Distinguishing separate primary lung carcinomas (SPLCs) from intrapulmonary metastases (IPMs) in non-small cell lung cancer (NSCLC) patients is a challenging dilemma in clinical practice. Next-generation sequencing (NGS) was recently shown to represent a robust molecular method for clonal discrimination in this setting. In this study, using clonal relationships established by comprehensive NGS as the ground truth, we investigated whether NSCLC patients with SPLCs versus IPMs exhibit distinct imaging characteristics.
This retrospective study included patients who underwent pre-treatment computed tomography (CT) and/or positron emission tomography/CT (PET/CT) imaging followed by surgical resection for >1 NSCLC. Nodular, parenchymal, pleural, and ancillary CT features, as well as maximum standardized uptake values (SUVs) on PET/CT were recorded. Rao-Scott chi-square, Wilcoxon rank-sum, and Fisher's exact tests were used in patient- and lesion-level comparisons.
This study included 60 patients (median age = 69 years, 68 % female) with 127 individual tumors comprising 51 SPLC vs 23 IPM tumor pairs based on NGS profiling. SPLCs were associated with subsolid consistency (P = 0.005) and spiculated contours (P < 0.001), while IPMs were associated with greater difference of size between lesions (P = 0.017) or pure solid consistency of the smaller lesion (P = 0.011). Lymph node involvement was more frequent in IPMs than SPLCs (P = 0.036). SUV measurements were not useful for differentiation (P > 0.05).
Selected preoperative CT features are distributed differentially in SPLCs and IPMs, suggesting that imaging may have a role in distinguishing clonal relationships of tumors in patients with >1 NSCLC.
在非小细胞肺癌(NSCLC)患者中,区分原发性肺肿瘤(SPLCs)和肺内转移(IPMs)是临床实践中的一个具有挑战性的难题。最近的研究表明,下一代测序(NGS)代表了一种在这种情况下进行克隆区分的强大分子方法。在这项研究中,我们使用综合 NGS 确定的克隆关系作为真实情况,研究了 SPLCs 与 IPMs 的 NSCLC 患者是否表现出不同的影像学特征。
本回顾性研究纳入了接受过治疗前计算机断层扫描(CT)和/或正电子发射断层扫描/CT(PET/CT)成像,随后接受>1 个 NSCLC 手术切除的患者。记录结节、实质、胸膜和辅助 CT 特征,以及 PET/CT 上的最大标准化摄取值(SUVs)。在患者和病变水平比较中使用 Rao-Scott 卡方检验、Wilcoxon 秩和检验和 Fisher 精确检验。
本研究纳入了 60 名患者(中位年龄 69 岁,68%为女性),127 个肿瘤包括 51 个 SPLC 和 23 个 IPM 肿瘤对,基于 NGS 分析。SPLCs 与亚实性一致性(P=0.005)和分叶状轮廓(P<0.001)相关,而 IPMs 与病变之间大小差异更大(P=0.017)或较小病变的纯实性一致性(P=0.011)相关。IPMs 比 SPLCs 更常伴有淋巴结受累(P=0.036)。SUV 测量对鉴别无帮助(P>0.05)。
在 SPLCs 和 IPMs 中,选定的术前 CT 特征分布不同,提示影像学可能在区分>1 个 NSCLC 患者肿瘤的克隆关系方面具有一定作用。