Relationship between lymphovascular invasion and molecular subtypes in invasive breast cancer

Purpose The aim of this study is to evaluate the relation between LVI and molecular subtypes in invasive breast cancers and to find out whether LVI which is a histopathologic indicator has a role in subtype classification or not. Methods One hundred and seventy‐six patients who had mastectomy for br...

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Published inInternational journal of clinical practice (Esher) Vol. 75; no. 4; pp. e13897 - n/a
Main Authors Morkavuk, Şevket Barış, Güner, Murat, Çulcu, Serdar, Eroğlu, Aydan, Bayar, Sancar, Ünal, Ali Ekrem
Format Journal Article
LanguageEnglish
Published England Hindawi Limited 01.04.2021
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Summary:Purpose The aim of this study is to evaluate the relation between LVI and molecular subtypes in invasive breast cancers and to find out whether LVI which is a histopathologic indicator has a role in subtype classification or not. Methods One hundred and seventy‐six patients who had mastectomy for breast cancer between 2013 and 2018 in the Department of Surgical Oncology, Faculty of Medicine, Ankara University were retrospectively analysed. One hundred and thirty‐two patients who had LVI, ER, PR, Her 2 and Ki‐67 index status information provided in their pathology results were included in the study. The relationship between molecular subtypes and LVI was investigated. Results One hundred and thirty‐two patients were analysed retrospectively. Eighty‐two patients had LVI and 50 patients had not. We found a relationship between Luminal B with Her2(−) and LVI, basal like and LVI (P = .00). No significant statistical difference was found between LVI and other molecular subtypes. We confirmed these results with multiple variable analysis (%77.3 correlation). Conclusions As a result, we found that LVI can affect molecular subtypes. This showed that a histopathological factor may affect tumour biology. In other words, breast cancer is a heterogeneous disease with many different predictors and prognostic variables.
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ISSN:1368-5031
1742-1241
DOI:10.1111/ijcp.13897