Division of Pathology, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Kashiwa, Chiba, Japan; Department of Thoracic Surgery, National Cancer Center Hospital, Kashiwa, Chiba, Japan; Department of Pathology and Clinical Laboratories, National Cancer Center Hospital East, Kashiwa, Japan; Departments of General Thoracic Surgery, Juntendo University School of Medicine, Tokyo, Japan.
Department of Thoracic Surgery, National Cancer Center Hospital, Kashiwa, Chiba, Japan.
Lung Cancer. 2018 Dec;126:162-169. doi: 10.1016/j.lungcan.2018.11.006. Epub 2018 Nov 6.
Lung cancer with usual interstitial pneumonia (UIP) pattern is a disease with poor prognosis. This study aimed to characterize the tumor microenvironment of lung adenocarcinoma associated with UIP (UIP-ADC).
A total of 1341 consecutive patients with ADC who had undergone complete surgical resection were enrolled in this study, and the clinicopathological features of UIP-ADC were examined. Further, we selected 17 cases of UIP-ADC and non-UIP ADC each (adjusted for age, smoking status, pathological stage, and invasive size of lesion) for immunohistochemical analysis, and the biological differences between UIP-ADC and non-UIP ADC groups were analyzed.
UIP-ADC was detected in 18 patients (1.3%). Patients with UIP-ADC had shorter cancer-specific survival (CSS) (5 yrs CSS; UIP-ADC 52.9% vs non-UIP ADC 81.8%, p < 0.01). Evaluation of tumor-infiltrating lymphocytes (TILs) in cancer stroma showed that the number of CD8 TILs in UIP-ADC group was significantly lower than that in the non-UIP ADC group (median number 91 vs 121, p < 0.01). In contrast, levels of Foxp3 TILs were not significantly different between the two groups. The CD8/Foxp3 T cell ratio was significantly lower in UIP-ADC than in the non-UIP ADC population (1.9 vs 2.7, p < 0.01). Additionally, among UIP-ADC patients, the CD8/Foxp3 T cell ratio was significantly higher in the non-cancerous UIP lesions than in the cancer stroma from the same patient (2.4 vs 1.7, p < 0.01).
In the current study, we have demonstrated that the tumor microenvironment of UIP-ADC acquires an immunosuppressive state, and this could be one of the possible explanations for poor prognosis of this disease.
具有普通间质性肺炎(UIP)模式的肺癌是一种预后不良的疾病。本研究旨在描述与 UIP 相关的肺腺癌(UIP-ADC)的肿瘤微环境。
本研究共纳入 1341 例接受完全手术切除的连续 ADC 患者,并检查 UIP-ADC 的临床病理特征。进一步,我们选择了每个 17 例 UIP-ADC 和非 UIP ADC(根据年龄、吸烟状态、病理分期和病变侵袭大小进行调整)进行免疫组织化学分析,并分析 UIP-ADC 和非 UIP ADC 组之间的生物学差异。
在 18 例患者(1.3%)中检测到 UIP-ADC。UIP-ADC 患者的癌症特异性生存率(CSS)更短(5 年 CSS;UIP-ADC 为 52.9%,而非 UIP ADC 为 81.8%,p<0.01)。对肿瘤浸润淋巴细胞(TILs)在癌症基质中的评估表明,UIP-ADC 组中 CD8 TILs 的数量明显低于非 UIP ADC 组(中位数为 91 对 121,p<0.01)。相比之下,两组之间 Foxp3 TILs 的水平没有显著差异。UIP-ADC 的 CD8/Foxp3 T 细胞比值明显低于非 UIP ADC 人群(1.9 对 2.7,p<0.01)。此外,在 UIP-ADC 患者中,同一患者的非癌性 UIP 病变中的 CD8/Foxp3 T 细胞比值明显高于癌基质(2.4 对 1.7,p<0.01)。
在目前的研究中,我们已经证明 UIP-ADC 的肿瘤微环境获得了免疫抑制状态,这可能是这种疾病预后不良的原因之一。