Population-based study of peritumoral lymphovascular invasion and outcome among patients with operable breast cancer

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Abstract

BackgroundLymphovascular invasion has been associated with poor prognosis in women with breast cancer, but it is unclear whether the presence of lymphovascular invasion should be considered sufficient to reclassify breast cancer patients who are at a low risk of recurrence into a high-risk category.MethodsOf the 16172 patients with operable breast cancer who were entered into the Danish Breast Cancer Cooperative Group Registry from January 1, 1996, to December 31, 2002, lymphovascular invasion was classified at primary diagnosis in 16121 patients as present (n=2453, 15%) or as absent (n=13206, 82%). Patients with at least one of the risk criteria (positive lymph nodes, tumor size >2 cm, high grade, hormone receptor-negative tumor, or younger than 35 years) were assigned to the high-risk group; the other patients were assigned to the low-risk group. All procedures, including report forms, central review, and querying, were specified in advance. Kaplan-Meier analyses were used to estimate disease-free intervals and overall survival rates among patients with and without lymphovascular invasion, and multivariable analysis was used to adjust for differences in baseline characteristics and therapy. All statistical tests were two-sided.ResultsComplete follow-up was achieved for 15659 patients. The median estimated potential follow-up was 6.4 years for invasive disease-free interval and 7.7 years for overall survival. Invasive disease-free interval and overall survival were statistically significantly associated with lymphovascular invasion within the high-risk group (hazard ratio [HR] for invasive disease=2.29, 95% confidence interval [CI]=2.14 to 2.45, P

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CITATION STYLE

APA

Ejlertsen, B., Jensen, M. B., Rank, F., Rasmussen, B. B., Christiansen, P., Kroman, N., … Mouridsen, H. T. (2009). Population-based study of peritumoral lymphovascular invasion and outcome among patients with operable breast cancer. Journal of the National Cancer Institute, 101(10), 729–735. https://doi.org/10.1093/jnci/djp090

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