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Analysis of complete response by MRI following neoadjuvant chemotherapy predicts pathological tumor responses differently for molecular subtypes of breast cancer

机译:新辅助化疗后通过MRI对完全反应的分析预测乳腺癌分子亚型的病理性肿瘤反应不同

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In the present study, clinical tumor response following neoadjuvant chemotherapy (NAC) was diagnosed by magnetic resonance imaging (MRI) and clinicopathological factors, including molecular subtypes at baseline, were analyzed for correlations with pathological tumor responses. In addition, clinicopathological factors were analyzed for a correlation with the MRI capacity to predict pathological complete response (pCR). Clinical tumor response evaluated by MRI following NAC was determined as a clinical CR (cCR) or a residual tumor. cCR was confirmed if no gadolinium enhancement or an enhancement equal to or less than that of glandular tissue was observed in any phase of the MRI. Pathological tumor responses following NAC were classified into grades 0 (no change) to 3 (no residual invasive cancer) according to criteria of the Japanese Breast Cancer Society. pCR was defined as grade 3 in the present study. Of 264 cases of invasive breast cancer in 260 patients (4 synchronous bilateral breast cancer cases), 59 (22%) were diagnosed by MRI following NAC as cCR and 98 (37%) were pathologically diagnosed as pCR. In terms of predicting pCR by MRI, the sensitivity, specificity, accuracy, positive predictive value (PPV) and negative predictive value (NPV) were 44, 90, 73, 73 and 73%, respectively. Tumor size, hormone receptor status, human epidermal growth factor receptor 2 (HER2) status, molecular subtype and histological type were significantly correlated with pathological tumor responses. pCR rates increased in the following order: luminal/HER2-negative (14%), luminal/HER2-positive (32%), triple-negative (46%) and non-luminal/HER2-positive (73%) tumors. Sensitivity and specificity were the highest (60 and 100%, respectively) in triple-negative tumors. PPV decreased in the following order: triple-negative (100%), non-luminal/HER2-positive (92%), luminal/HER2-positive (46%) and luminal/HER2-negative (33%) tumors. In conclusion, MRI evaluation is useful for predicting pCR following NAC, particularly for triple-negative tumors.
机译:在本研究中,通过磁共振成像(MRI)诊断了新辅助化疗(NAC)后的临床肿瘤反应,并分析了包括基线分子亚型在内的临床病理因素与病理肿瘤反应的相关性。此外,分析了临床病理因素与MRI预测病理完全缓解(pCR)能力的相关性。 NAC后通过MRI评估的临床肿瘤反应被确定为临床CR(cCR)或残留肿瘤。如果在MRI的任何阶段均未观察到g增强或等于或小于腺组织的增强,则可以确认cCR。根据日本乳腺癌学会的标准,NAC后的病理性肿瘤反应分为0级(无变化)至3级(无残留浸润癌)。在本研究中,pCR被定义为3级。在260例患者中的264例浸润性乳腺癌中(4例同时发生的双侧乳腺癌),在NAC后经MRI诊断为cCR的为59例(22%),在病理学上诊断为pCR的为98例(37%)。就通过MRI预测pCR而言,敏感性,特异性,准确性,阳性预测值(PPV)和阴性预测值(NPV)分别为44%,90%,73%,73%和73%。肿瘤大小,激素受体状态,人类表皮生长因子受体2(HER2)状态,分子亚型和组织学类型与病理性肿瘤反应显着相关。 pCR率按以下顺序增加:管腔/ HER2阴性(14%),管腔/ HER2阳性(32%),三管阴性(46%)和非管腔/ HER2阳性(73%)肿瘤。在三阴性肿瘤中,敏感性和特异性最高(分别为60%和100%)。 PPV按以下顺序降低:三阴性(100%),非管腔/ HER2阳性(92%),管腔/ HER2阳性(46%)和管腔/ HER2阴性(33%)。总之,MRI评估可用于预测NAC后的pCR,特别是对于三阴性肿瘤。

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