Abstract

BackgroundDuctal carcinoma in situ with microinvasion (DCIS-Mi) generally has favorable prognosis, but the long-term outcomes of DCIS-Mi and the biologic evolution from ductal carcinoma in situ (DCIS), DCIS-Mi, to DCIS with T1a breast cancer (DCIS-T1a) has not been specified. The aim of our study was to explore the biological and prognostic features of DCIS-Mi, compared with pure DCIS and DCIS-T1a.ResultsAfter a median follow-up of 31 months, the 3-year estimated disease free survival(DFS) rate of DCIS-Mi patients was significantly lower than that of pure DCIS patients (89.5% vs 97.1%, P=0.009). Patients with DCIS-Mi or DCIS-T1a tumors had comparable 3-year estimated DFS rates (89.5% vs 94.3%, P=0.13). No significant difference in overall survival (OS) was found among different groups (99.6%, 100% and 99.1% for DCIS, DCIS-Mi and DCIS-T1a, P=0.797). In chemotherapy and trastuzumab-naive DCIS-Mi patients, human epidermal growth factor receptor2 (HER2) positivity (HR=21.8, 95%CI, 1.7-286.8, P=0.019) were independent predictor of worse DFS on multivariate analysis.MethodsDuring September 2002 and December 2014, 602 breast cancer patients who underwent radical surgery were retrospectively reviewed. Three hundred and fifty-nine patients (59.6%) had pure DCIS, 84(14.0%) and 159(26.4%) were diagnosed as DCIS-Mi and DCIS-T1a. Clinico-pathological features were compared between different subgroups.ConclusionsDCIS-Mi displayed a comparable survival to that of DCIS-T1a and a more aggressive biological nature than pure DCIS. Patients with HER2-positive DCIS-Mi had a worse survival and adjuvant chemotherapy plus target therapy needs to be further optimized in those patients.

Highlights

  • Patients with human epidermal growth factor receptor2 (HER2)-positive DCISMi had a worse survival and adjuvant chemotherapy plus target therapy needs to be further optimized in those patients

  • According to the staging system of the American Joint Committee on Cancer (AJCC), ductal carcinoma in situ with microinvasion (DCIS-Mi) was defined as ductal carcinoma in situ (DCIS) with a microscopic focus of invasion ≤1 mm in the longest diameter [1], which is identified in 10–20% of DCIS cases and accounts for approximately 1% of all breast cancers [2, 3]

  • Ductal carcinoma in situ with microinvasion (DCIS-Mi) tumors tended to exhibit the highest proportion of human epidermal growth factor receptor2 (HER2)-positive tumor (29.5% for DCIS, 42.9% for DCIS-Mi and 29.3% for DCIS-T1a, P=0.048)

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Summary

Introduction

According to the staging system of the American Joint Committee on Cancer (AJCC), ductal carcinoma in situ with microinvasion (DCIS-Mi) was defined as ductal carcinoma in situ (DCIS) with a microscopic focus of invasion ≤1 mm in the longest diameter [1], which is identified in 10–20% of DCIS cases and accounts for approximately 1% of all breast cancers [2, 3]. The natural history of cancer cells progression from DCIS to DCISMi, and to invasive ductal carcinoma (IDC) remains unclear, and DCIS-Mi may represent the interim stage in the evolutionary progress from DCIS to IDC. Ductal carcinoma in situ with microinvasion (DCIS-Mi) generally has favorable prognosis, but the long-term outcomes of DCIS-Mi and the biologic evolution from ductal carcinoma in situ (DCIS), DCIS-Mi, to DCIS with T1a breast cancer (DCIS-T1a) has not been specified. The aim of our study was to explore the biological and prognostic features of DCIS-Mi, compared with pure DCIS and DCIS-T1a

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