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      Increased Risk of Locoregional Recurrence for Women With T1-2N0 Triple-Negative Breast Cancer Treated With Modified Radical Mastectomy Without Adjuvant Radiation Therapy Compared With Breast-Conserving Therapy

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          Abstract

          Purpose

          To evaluate the risk of locoregional recurrence (LRR) associated with locoregional treatment of women with primary breast cancer tumors negative for estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (triple-negative breast cancer [TNBC]).

          Patients and Methods

          Patients diagnosed with TNBC were identified from a cancer registry in a single institution (n=768). LRR-free survival was estimated using Kaplan-Meier analysis. The Cox proportional hazards regression model was used to determine risk of LRR on the basis of locoregional management: breast-conserving therapy (BCT; ie, lumpectomy and adjuvant radiation therapy [RT]) and modified radical mastectomy (MRM) in the TNBC population and T1-2N0 subgroup.

          Results

          At a median follow-up of 7.2 years, 77 patients (10%) with TNBC developed LRR. Five-year LRR-free survival was 94%, 85%, and 87% in the BCT, MRM, and MRM + RT groups, respectively ( P < .001). In multivariate analysis, MRM (compared with BCT), lymphovascular invasion and lymph node positivity were associated with increased LRR. Conversely, adjuvant chemotherapy was associated with decreased risk of LRR. For patients with T1-2N0 tumors, 5-year LRR-free survival was 96% and 90% in the BCT and MRM groups, respectively ( P =.027), and MRM was the only independent prognostic factor associated with increased LRR compared with BCT (hazard ratio, 2.53; 95% CI, 1.12 to 5.75; P= .0264).

          Conclusion

          Women with T1-2N0 TNBC treated with MRM without RT have a significant increased risk of LRR compared with those treated with BCT. Prospective studies are warranted to investigate the benefit of adjuvant RT after MRM in TNBC.

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          Author and article information

          Journal
          J Clin Oncol
          J. Clin. Oncol
          jco
          jco
          JCO
          Journal of Clinical Oncology
          American Society of Clinical Oncology
          0732-183X
          1527-7755
          20 July 2011
          13 June 2011
          13 June 2011
          : 29
          : 21
          : 2852-2858
          Affiliations
          [1]All authors: Cross Cancer Institute and University of Alberta, Edmonton, Alberta, Canada.
          Author notes
          Corresponding author: Bassam Abdulkarim, MD, PhD, FRCPC, Department of Oncology, McGill University Montreal General Hospital, McGill University Health Centre, 1650 Cedar Avenue, Montreal, Quebec H3G 1A4, Canada; e-mail: bassam.abdulkarim@ 123456mcgill.ca .

          B.S.A. and J.C. contributed equally to this work.

          Article
          PMC5073381 PMC5073381 5073381 34714
          10.1200/JCO.2010.33.4714
          5073381
          21670451
          9242c2bb-f865-4d32-9bee-b36458f9a6e8
          © 2011 by American Society of Clinical Oncology
          History
          : 28 October 2010
          : 23 March 2011
          Categories
          Bc3
          Bc4
          Hung
          ORIGINAL REPORTS
          Breast Cancer

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