Zhang Meng, Yoshizawa Akihiko, Kawakami Satoshi, Asaka Shiho, Yamamoto Hiroshi, Yasuo Masanori, Agatsuma Hiroyuki, Toishi Masayuki, Shiina Takayuki, Yoshida Kazuo, Honda Takayuki, Ito Ken-Ichi
Division of Breast, Endocrine and Respiratory Surgery, Department of Surgery (II), Shinshu University School of Medicine, Matsumoto, Japan.
Department of Laboratory Medicine, Shinshu University Hospital, Matsumoto, Japan.
Cancer Med. 2016 Oct;5(10):2721-2730. doi: 10.1002/cam4.858. Epub 2016 Aug 21.
Combined pulmonary fibrosis and emphysema (CPFE) is an important risk factor for lung cancer (LC), because most patients with CPFE are smokers. However, the histological characteristics of LC in patients with CPFE (LC-CPFE) remain unclear. We conducted this study to explore the clinicopathological characteristics of LC-CPFE. We retrospectively reviewed data from 985 patients who underwent resection for primary LC, and compared the clinicopathological characteristics of patients with LC-CPFE and non-CPFE LC. We identified 72 cases of LC-CPFE, which were significantly associated with squamous cell carcinoma (SqCC) histology (n = 46, P < 0.001) and higher tumor grade (n = 44, P < 0.001), compared to non-CPFE LC. Most LC-CPFE lesions were contiguous with fibrotic areas around the tumor (n = 59, 81.9%), and this association was independent of tumor location. Furthermore, dysplastic epithelium was identified in the fibrotic area for 31 (52.5%) LC-CPFE lesions. Moreover, compared to patients with pulmonary fibrosis alone in the non-CPFE group (n = 31), patients with CPFE were predominantly male (P = 0.008) and smokers (P < 0.001), with LC-CPFE predominantly exhibiting SqCC histology (P = 0.010) and being contiguous with the tumor-associated fibrotic areas (P < 0.001). Multivariate analysis revealed that CPFE was an independent predictor of overall survival (hazard ratio: 1.734; 95% confidence interval: 1.060-2.791; P = 0.028). Our results indicate that LC-CPFE has a distinct histological phenotype, can arise from the dysplastic epithelium in the fibrotic area around the tumor, and is associated with poor survival outcomes.
合并性肺纤维化和肺气肿(CPFE)是肺癌(LC)的一个重要危险因素,因为大多数CPFE患者是吸烟者。然而,CPFE患者的肺癌(LC-CPFE)的组织学特征仍不清楚。我们进行了这项研究以探讨LC-CPFE的临床病理特征。我们回顾性分析了985例接受原发性肺癌切除术患者的数据,并比较了LC-CPFE患者和非CPFE肺癌患者的临床病理特征。我们确定了72例LC-CPFE,与非CPFE肺癌相比,其与鳞状细胞癌(SqCC)组织学(n = 46,P < 0.001)和更高的肿瘤分级(n = 44,P < 0.001)显著相关。大多数LC-CPFE病变与肿瘤周围的纤维化区域相邻(n = 59,81.9%),并且这种关联与肿瘤位置无关。此外,在31例(52.5%)LC-CPFE病变的纤维化区域中发现了发育异常的上皮。此外,与非CPFE组中仅患有肺纤维化的患者(n = 31)相比,CPFE患者以男性为主(P = 0.008)且为吸烟者(P < 0.001),LC-CPFE主要表现为SqCC组织学(P = 0.010)且与肿瘤相关的纤维化区域相邻(P < 0.001)。多变量分析显示CPFE是总生存的独立预测因素(风险比:1.734;95%置信区间:1.060 - 2.791;P = 0.028)。我们的结果表明,LC-CPFE具有独特的组织学表型,可起源于肿瘤周围纤维化区域的发育异常上皮,并且与不良生存结果相关。