4.5 Article

Collagen Organization in Relation to Ductal Carcinoma In Situ Pathology and Outcomes

Journal

CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
Volume 30, Issue 1, Pages 80-88

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1055-9965.EPI-20-0889

Keywords

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Funding

  1. NCI [U01 CA196383, U54 CA163303, P01 CA154292, R01 CA199996, P30 CA014520]
  2. Patient-Centered Outcomes Research Institute (PCORI) [PCS1504-30370]
  3. University of Vermont Cancer Center
  4. Lake Champlain Cancer Research Organization [032800]
  5. Centers for Disease Control and Prevention [NU58DP006322]

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The study found associations between collagen fiber features in the DCIS tumor microenvironment and pathological characteristics and patient outcomes. After adjustment for treatments and nuclear grade, greater collagen fiber width and density were associated with lower risk of recurrence, while higher fiber straightness and distance to the nearest two fibers were linked to increased risk. Additionally, composite factors identified through factor analysis were inversely associated with recurrence risk.
Background: There is widespread interest in discriminating indolent from aggressive ductal carcinoma in situ (DCIS). We sought to evaluate collagen organization in the DCIS tumor microenvironment in relation to pathologic characteristics and patient outcomes. Methods: We retrieved fixed tissue specimens for 90 DCIS cases within the population-based Vermont DC1S Cohort. We imaged collagen fibers within 75 mu m 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. Results: Multiple collagen features were associated with DCIS grade, necrosis pattern, or periductal fibrosis (P < 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 (P > 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; P <= 0.01). Conclusions: Multiple aspects of collagen organization around DCIS lesions are associated with recurrence risk. Impact: Collagen organization should be considered in the development of prognostic DCIS biomarker signatures.

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