Prognostic Markers and Long-Term Outcomes in Ductal Carcinoma In Situ of the Breast Treated With Excision Alone

被引:34
作者
Holmes, Phoebe [1 ]
Lloyd, Joshua [1 ]
Chervoneva, Inna [2 ]
Pequinot, Edward [2 ]
Cornfield, Dennis B. [3 ]
Schwartz, Gordon F. [4 ]
Allen, Kathleen G. [5 ]
Palazzo, Juan P. [1 ]
机构
[1] Thomas Jefferson Univ Hosp, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Div Clin Pharmacol, Biostat Sect, Philadelphia, PA 19107 USA
[3] Lehigh Valley Hosp, Hlth Network Labs, Dept Pathol, Allentown, PA USA
[4] Thomas Jefferson Univ Hosp, Dept Surg, Philadelphia, PA 19107 USA
[5] Morton Plant Hosp, Comprehens Breast Care Ctr Tampa Bay, Clearwater, FL USA
关键词
ductal carcinoma in situ; breast conservation surgery; prognostic markers; CONSERVING SURGERY; RADIATION-THERAPY; LOCAL RECURRENCE; NATURAL-HISTORY; CANCER; TUMORS; WOMEN; CONSERVATION; EXPRESSION; LUMPECTOMY;
D O I
10.1002/cncr.25942
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Increased use of breast cancer screening has led to an increase in the number of diagnosed cases of ductal carcinoma in situ (DCIS). However, there is no definite way to predict progression or recurrence of DCIS. We analyzed the significance of biological markers and tumor characteristics in predicting recurrence in a large series of DCIS patients with long-term follow-up treated with breast conservation surgery (BCS) alone. METHODS: Clinical and pathological data were analyzed for 141 patients who underwent BCS for DCIS. All had negative surgical margins. Using local disease recurrence as an endpoint, we sought to determine the prognostic significance of several histopathological characteristics (tumor size, presence of necrosis, and subtype) and biological markers (estrogen receptor, progesterone receptor, and Her-2/neu.) RESULTS: At a median follow-up of 122 months (maximum follow-up, 294 months), 60 recurrences occurred, with a median time to recurrence of 191 months. On multivariate analysis, Her-2 positivity (3+) was found to be significantly associated with reduced time to tumor recurrence (P = .028). Tumor size and higher grade were marginally statistically significant (P = .099, P = .070). Neither necrosis nor tumor pathological characteristics were found to be significantly related to time to disease recurrence. CONCLUSIONS: Our results suggested that status of Her-2/neu, larger tumor size, and higher nuclear grade were significantly correlated with time to tumor recurrence in patients treated with BCS alone. Using logistical analyses, no significant correlation was found between tumor pathological characteristics and disease recurrence. Cancer 2011;117:3650-7. (C) 2011 American Cancer Society.
引用
收藏
页码:3650 / 3657
页数:8
相关论文
共 38 条
[1]   Prognostic Significance of Oncogenic Markers in Ductal Carcinoma In Situ of the Breast: A Clinicopathologic Study [J].
Altintas, Sevilay ;
Lambein, Kathleen ;
Huizing, Manon T. ;
Braems, Geert ;
Asjoe, Fernando Tjin ;
Hellemans, Hilde ;
Van Marck, Eric ;
Weyler, Joost ;
Praet, Marleen ;
Van den Broecke, Rudy ;
Vermorken, Jan B. ;
Tjalma, Wiebren A. .
BREAST JOURNAL, 2009, 15 (02) :120-132
[2]   Prediction of local recurrence of ductal carcinoma in situ of the breast using five histological classifications:: A comparative study with long follow-up [J].
Badve, S ;
A'Hern, RP ;
Ward, AM ;
Millis, RR ;
Pinder, SE ;
Ellis, IO ;
Gusterson, BA ;
Sloane, JP .
HUMAN PATHOLOGY, 1998, 29 (09) :915-923
[3]   Molecular Grading of Ductal Carcinoma In situ of the Breast [J].
Balleine, Rosemary L. ;
Webster, Lucy R. ;
Davis, Sean ;
Salisbury, Elizabeth L. ;
Palazzo, Juan P. ;
Schwartz, Gordon F. ;
Cornfield, Dennis B. ;
Walker, Robert L. ;
Byth, Karen ;
Clarke, Christine L. ;
Meltzer, Paul S. .
CLINICAL CANCER RESEARCH, 2008, 14 (24) :8244-8252
[4]   Trends in the treatment of ductal carcinoma in situ of the breast [J].
Baxter, NN ;
Virnig, BA ;
Durham, SB ;
Tuttle, TM .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (06) :443-448
[5]   Breast-conserving treatment with or without radiotherapy in ductal carcinoma-in-situ: Ten-Year results of European Organisation for Research and Treatment of Cancer randomized phase III trial 10853 - A study by the EORTC Breast Cancer Cooperative Group and EORTC Radiotherapy Group [J].
Bijker, Nina ;
Meijnen, Philip ;
Peterse, Johannes L. ;
Bogaerts, Jan ;
Van Hoorebeeck, Irene ;
Julien, Jean-Pierre ;
Gennaro, Massimiliano ;
Rouanet, Philippe ;
Avril, Antoine ;
Fentiman, Ian S. ;
Bartelink, Harry ;
Rutgers, Emiel J. Th. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (21) :3381-3387
[6]   Separate cavity margin sampling at the time of initial breast lumpectomy significantly reduces the need for reexcisions [J].
Cao, DF ;
Lin, C ;
Woo, SH ;
Vang, R ;
Tsangaris, TN ;
Argani, P .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2005, 29 (12) :1625-1632
[7]   The prognostic significance of multiple morphologic features and biologic markers in ductal carcinoma in situ of the breast - A study of a large cohort of patients treated with surgery alone [J].
Cornfield, DB ;
Palazzo, JP ;
Schwartz, GF ;
Goonewardene, SA ;
Kovatich, AJ ;
Chervoneva, I ;
Hyslop, T ;
Schwarting, R .
CANCER, 2004, 100 (11) :2317-2327
[8]   Targeting HER-2/neu in early breast cancer development using dendritic cells with staged interleukin-12 burst secretion [J].
Czerniecki, Brian J. ;
Koski, Gary K. ;
Koldovsky, Ursula ;
Xu, Shuwen ;
Cohen, Peter A. ;
Mick, Rosemarie ;
Nisenbaum, Harvey ;
Pasha, Terry ;
Xu, Min ;
Fox, Kevin R. ;
Weinstein, Susan ;
Orel, Susan G. ;
Vonderheide, Robert ;
Coukos, George ;
DeMichele, Angela ;
Araujo, Louis ;
Spitz, Francis R. ;
Rosen, Mark ;
Levine, Bruce L. ;
June, Carl ;
Zhang, Paul J. .
CANCER RESEARCH, 2007, 67 (04) :1842-1852
[9]   Effect of Margin Status on Local Recurrence After Breast Conservation and Radiation Therapy for Ductal Carcinoma In Situ [J].
Dunne, Clive ;
Burke, John P. ;
Morrow, Monica ;
Kell, Malcolm R. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (10) :1615-1620
[10]   The natural history of ductal carcinoma in situ of the breast:: a review [J].
Erbas, B ;
Provenzan, E ;
Armes, J ;
Gertig, D .
BREAST CANCER RESEARCH AND TREATMENT, 2006, 97 (02) :135-144