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   <subfield code="a">10.1245/s10434-011-1920-z</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1245/s10434-011-1920-z</subfield>
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   <subfield code="a">Triple-Negative Breast Cancer Is Not a Contraindication for Breast Conservation</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Farrell Adkins, Ana Gonzalez-Angulo, Xiudong Lei, Leonel Hernandez-Aya, Elizabeth Mittendorf, Jennifer Litton, Jamie Wagner, Kelly Hunt, Wendy Woodward, Funda Meric-Bernstam]</subfield>
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   <subfield code="a">Background: Triple-negative breast cancer (TNBC) is an aggressive subtype shown to have a high risk of locoregional recurrence (LRR). The purpose of this study was to determine the impact of operation type on LRR in TNBC patients. Methods: A total of 1325 patients with TNBC who underwent breast-conserving therapy (BCT) or mastectomy from 1980 to the present were identified. Clinical and pathological factors were compared by the chi-square test. LRR-free survival (LRRFS), distant metastasis-free survival, and overall survival were estimated by the Kaplan-Meier method. Multivariate analysis was performed by the Cox proportional hazard models. Results: BCT was performed in 651 patients (49%) and mastectomy in 674 (51%). The mastectomy group had larger tumors, a higher incidence of lymphovascular invasion, and higher pathologic N stage (all P&lt;0.001). At 62-month median follow-up, LRR was seen in 170 (26%) in the BCT group and 203 (30%) in the mastectomy group. Five-year LRRFS rates were higher in the BCT group (76% vs. 71%, P=0.032), as was distant metastasis-free survival (68% vs. 54%, P&lt;0.0001) and overall survival (74% vs. 63%, P&lt;0.0001). On multivariate analysis, T stage (hazard ratio [HR] 1.37, P=0.006), high nuclear grade (HR 1.92, P=0.002), lymphovascular invasion (HR 1.93, P&lt;0.0001), close/positive margins (HR 1.89, P&lt;0.0001), and use of non-anthracycline or taxane-based adjuvant chemotherapy (HR 2.01, P&lt;0.0001) increased the LRR risk, while age &gt;50years was protective (HR 0.73, P=0.007). Operation type (mastectomy vs. BCT, HR 1.07, P=0.55) was not statistically significant. Conclusions: BCT is not associated with increased LRR rates compared to mastectomy. TNBC should not be considered a contraindication for breast conservation.</subfield>
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   <subfield code="a">Society of Surgical Oncology, 2011</subfield>
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   <subfield code="a">Adkins</subfield>
   <subfield code="D">Farrell</subfield>
   <subfield code="u">Department of Surgical Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, USA</subfield>
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   <subfield code="a">Gonzalez-Angulo</subfield>
   <subfield code="D">Ana</subfield>
   <subfield code="u">Department Breast Medical Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, USA</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Lei</subfield>
   <subfield code="D">Xiudong</subfield>
   <subfield code="u">Department of Biostatistics, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, USA</subfield>
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   <subfield code="a">Hernandez-Aya</subfield>
   <subfield code="D">Leonel</subfield>
   <subfield code="u">Department Breast Medical Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, USA</subfield>
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   <subfield code="a">Mittendorf</subfield>
   <subfield code="D">Elizabeth</subfield>
   <subfield code="u">Department of Surgical Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, USA</subfield>
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   <subfield code="a">Litton</subfield>
   <subfield code="D">Jennifer</subfield>
   <subfield code="u">Department Breast Medical Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, USA</subfield>
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   <subfield code="a">Wagner</subfield>
   <subfield code="D">Jamie</subfield>
   <subfield code="u">Department of Surgical Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, USA</subfield>
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   <subfield code="a">Hunt</subfield>
   <subfield code="D">Kelly</subfield>
   <subfield code="u">Department of Surgical Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, USA</subfield>
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   <subfield code="a">Woodward</subfield>
   <subfield code="D">Wendy</subfield>
   <subfield code="u">Department of Radiation Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, USA</subfield>
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   <subfield code="u">Department of Surgical Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, TX, USA</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
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   <subfield code="g">18/11(2011-10-01), 3164-3173</subfield>
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