Lee Su Hyun, Chang Jung Min, Shin Sung Ui, Chu A Jung, Yi Ann, Cho Nariya, Moon Woo Kyung
1 Department of Radiology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
2 Department of Radiology, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Korea.
Br J Radiol. 2017 Dec;90(1080):20170470. doi: 10.1259/bjr.20170470. Epub 2017 Oct 9.
To evaluate imaging features of breast cancers on digital breast tomosynthesis (DBT) according to molecular subtype and to determine whether the molecular subtype affects breast cancer detection on DBT.
This was an institutional review board--approved study with a waiver of informed consent. DBT findings of 288 invasive breast cancers were reviewed according to Breast Imaging Reporting and Data System lexicon. Detectability of breast cancer was quantified by the number of readers (0-3) who correctly detected the cancer in an independent blinded review. DBT features and the cancer detectability score according to molecular subtype were compared using Fisher's exact test and analysis of variance.
Of 288 invasive cancers, 194 were hormone receptor (HR)-positive, 48 were human epidermal growth factor receptor 2 (HER2) positive and 46 were triple negative breast cancers. The most common DBT findings were irregular spiculated masses for HR-positive cancer, fine pleomorphic or linear branching calcifications for HER2 positive cancer and irregular masses with circumscribed margins for triple negative breast cancers (p < 0.001). Cancer detectability on DBT was not significantly different according to molecular subtype (p = 0.213) but rather affected by tumour size, breast density and presence of mass or calcifications.
Breast cancers showed different imaging features according to molecular subtype; however, it did not affect the cancer detectability on DBT. Advances in knowledge: DBT showed characteristic imaging features of breast cancers according to molecular subtype. However, cancer detectability on DBT was not affected by molecular subtype of breast cancers.
根据分子亚型评估数字乳腺断层合成(DBT)上乳腺癌的影像特征,并确定分子亚型是否影响DBT对乳腺癌的检测。
本研究经机构审查委员会批准,豁免知情同意。根据乳腺影像报告和数据系统词典对288例浸润性乳腺癌的DBT检查结果进行回顾。在独立的盲法评估中,通过正确检测到癌症的读者数量(0 - 3名)对乳腺癌的可检测性进行量化。使用Fisher精确检验和方差分析比较DBT特征以及根据分子亚型的癌症可检测性评分。
在288例浸润性癌中,194例为激素受体(HR)阳性,48例为人表皮生长因子受体2(HER2)阳性,46例为三阴性乳腺癌。最常见的DBT表现为HR阳性癌呈不规则毛刺状肿块,HER2阳性癌为细多形性或线性分支钙化,三阴性乳腺癌为边缘清晰的不规则肿块(p < 0.001)。根据分子亚型,DBT对癌症的可检测性无显著差异(p = 0.213),而是受肿瘤大小、乳腺密度以及肿块或钙化的存在影响。
乳腺癌根据分子亚型表现出不同的影像特征;然而,这并不影响DBT对癌症的可检测性。知识进展:DBT根据分子亚型显示出乳腺癌的特征性影像特征。然而,DBT对癌症的可检测性不受乳腺癌分子亚型的影响。