Department of Surgery, Office of Health Promotion Research, University of Vermont Larner College of Medicine, Burlington, Vermont.
University of Vermont Cancer Center, University of Vermont Larner College of Medicine, Burlington, Vermont.
Cancer Epidemiol Biomarkers Prev. 2021 Jan;30(1):80-88. doi: 10.1158/1055-9965.EPI-20-0889. Epub 2020 Oct 20.
There is widespread interest in discriminating indolent from aggressive ductal carcinoma (DCIS). We sought to evaluate collagen organization in the DCIS tumor microenvironment in relation to pathologic characteristics and patient outcomes.
We retrieved fixed tissue specimens for 90 DCIS cases within the population-based Vermont DCIS Cohort. We imaged collagen fibers within 75 μm of the tumor/stromal boundary on hematoxylin and eosin-stained slides using multiphoton microscopy with second-harmonic generation. Automated software quantified collagen fiber length, width, straightness, density, alignment, and angle to the tumor/stroma boundary. Factor analysis identified linear combinations of collagen fiber features representing composite attributes of collagen organization.
Multiple collagen features were associated with DCIS grade, necrosis pattern, or periductal fibrosis ( < 0.05). After adjusting for treatments and nuclear grade, risk of recurrence (defined as any second breast cancer diagnosis) was lower among cases with greater collagen fiber width [hazard ratio (HR), 0.57 per one standard deviation increase; 95% confidence interval (CI), 0.39-0.84] and fiber density (HR, 0.60; 95% CI, 0.42-0.85), whereas risk was elevated among DCIS cases with higher fiber straightness (HR, 1.47; 95% CI, 1.05-2.06) and distance to the nearest two fibers (HR, 1.47; 95% CI, 1.06-2.02). Fiber length, alignment, and fiber angle were not associated with recurrence ( > 0.05). Five composite factors were identified, accounting for 72.4% of the total variability among fibers; three were inversely associated with recurrence (HRs ranging from 0.60 to 0.67; ≤ 0.01).
Multiple aspects of collagen organization around DCIS lesions are associated with recurrence risk.
Collagen organization should be considered in the development of prognostic DCIS biomarker signatures.
鉴别惰性和侵袭性导管癌(DCIS)具有广泛的意义。我们试图评估 DCIS 肿瘤微环境中的胶原组织与病理特征和患者结局的关系。
我们从基于人群的佛蒙特州 DCIS 队列中检索了 90 例 DCIS 病例的固定组织标本。我们使用双光子显微镜和二次谐波产生,对苏木精和伊红染色载玻片上肿瘤/基质边界 75μm 内的胶原纤维进行成像。自动化软件定量了胶原纤维的长度、宽度、直线度、密度、排列和与肿瘤/基质边界的角度。因子分析确定了胶原纤维特征的线性组合,代表胶原组织复合属性。
多个胶原特征与 DCIS 分级、坏死模式或周围纤维组织增生有关(<0.05)。在校正了治疗和核分级后,具有较宽胶原纤维[风险比(HR),每增加一个标准差增加 0.57;95%置信区间(CI),0.39-0.84]和纤维密度(HR,0.60;95%CI,0.42-0.85)的病例复发风险较低,而胶原纤维直线度较高(HR,1.47;95%CI,1.05-2.06)和与最近两根纤维的距离较高(HR,1.47;95%CI,1.06-2.02)的 DCIS 病例风险增加。纤维长度、排列和纤维角度与复发无关(>0.05)。确定了 5 个综合因素,占纤维总变异性的 72.4%;其中 3 个与复发呈负相关(HR 范围为 0.60 至 0.67;≤0.01)。
DCIS 病变周围的胶原组织多个方面与复发风险相关。
胶原组织应在开发用于预测 DCIS 生物标志物特征的方案中得到考虑。