Author:
Kader Tanjina,Provenzano Elena,Jayawardana Madawa W.,Hendry Shona,Pang Jia-Min,Elder Kenneth,Byrne David J.,Tjoeka Lauren,Frazer Helen ML.,House Eloise,Jayasinghe Sureshni I.,Keane Holly,Murugasu Anand,Rajan Neeha,Miligy Islam M.,Toss Michael,Green Andrew R.,Rakha Emad A.,Fox Stephen B.,Mann G. Bruce,Campbell Ian G.,Gorringe Kylie L.
Abstract
AbstractVarious histopathological, clinical and imaging parameters have been evaluated to identify a subset of women diagnosed with lesions with uncertain malignant potential (B3 or BIRADS 3/4A lesions) who could safely be observed rather than being treated with surgical excision, with little impact on clinical practice. The primary reason for surgery is to rule out an upgrade to either ductal carcinoma in situ or invasive breast cancer, which occurs in up to 30% of patients. We hypothesised that the stromal immune microenvironment could indicate the presence of carcinoma associated with a ductal B3 lesion and that this could be detected in biopsies by counting lymphocytes as a predictive biomarker for upgrade. A higher number of lymphocytes in the surrounding specialised stroma was observed in upgraded ductal and papillary B3 lesions than non-upgraded (p < 0.01, negative binomial model, n = 307). We developed a model using lymphocytes combined with age and the type of lesion, which was predictive of upgrade with an area under the curve of 0.82 [95% confidence interval 0.77–0.87]. The model can identify some patients at risk of upgrade with high sensitivity, but with limited specificity. Assessing the tumour microenvironment including stromal lymphocytes may contribute to reducing unnecessary surgeries in the clinic, but additional predictive features are needed.
Funder
Cancer Australia
National Breast Cancer Foundation
University of Melbourne
Peter MacCallum Foundation
Cancer Council Victoria
National Health and Medical Research Council
Union for International Cancer Control
Australian Cancer Research Foundation
Publisher
Springer Science and Business Media LLC