Identifying the impact of inflammatory breast cancer on survival: a retrospective multi-center cohort study

被引:5
作者
Diessner, J. [1 ]
Van Ewijk, R. [3 ]
Weiss, C. R. [1 ]
Janni, W. [2 ]
Wischnewsky, M. B. [4 ]
Kreienberg, R. [2 ]
Hancke, K. [2 ]
Blettner, M. [3 ]
Woeckel, A. [1 ]
Schwentner, L. [2 ]
机构
[1] Univ Wurzburg, Dept Obstet & Gynecol, Sch Med, D-97080 Wurzburg, Germany
[2] Univ Ulm, Dept Obstet & Gynecol, Sch Med, D-89075 Ulm, Germany
[3] Johannes Gutenberg Univ Mainz, Dept Obstet & Gynecol, Sch Med, D-55131 Mainz, Germany
[4] Univ Bremen, Fac Math Comp Sci, D-28359 Bremen, Germany
关键词
Inflammatory breast cancer; Overall survival; Her2; Expression; Hormone receptor expression; BRENDA; NEOADJUVANT CHEMOTHERAPY; MOLECULAR-BIOLOGY; RECEPTOR STATUS; OPEN-LABEL; CARCINOMA; TRASTUZUMAB; THERAPY; WOMEN; EXPRESSION; PACLITAXEL;
D O I
10.1007/s00404-015-3691-4
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Inflammatory breast cancer (IBC) represents a rare and aggressive form of cancer with negative prognosis and high rate of recurrence. The purpose of this retrospective multi-center study was to evaluate the effect of IBC on overall and disease-free survival. Furthermore we analyzed the influence of hormone and Her2 receptor expression on inflammatory breast cancer cells on the clinical outcome of patients. This retrospective German multi-center study included 11,780 patients with primary breast cancer recruited from 1992 to 2008. In this sub-group analysis we focused on 70 patients with IBC. Despite the relatively small sample size, we could confirm the aggressiveness of inflammatory breast cancer and the different clinical behavior of IBC subtypes. It could be demonstrated that the lack of expression of hormone receptors on tumor cells is associated with a more aggressive clinical course and decreased overall and disease-free survival. Higher incidence of Her2 overexpression, that is typically associated with poor prognostic outcome among women with non-IBC tumors, seems however to have no prognostic significance. This BRENDA sub-group analysis, on a German cohort of breast cancer patients confirmed the negative outcome of IBC and the different clinical behavior of IBC subtypes. The best management of IBC requires intensive coordination and cooperation between various clinical disciplines involved in the treatment of IBC patients. Moreover there is a need to identify IBC-specific targeted therapies to improve the curing prospects of this subtype of cancer.
引用
收藏
页码:655 / 664
页数:10
相关论文
共 52 条
[1]  
Baldini Editta, 2004, Clin Breast Cancer, V5, P358, DOI 10.3816/CBC.2004.n.042
[2]   Gene expression profiles of inflammatory breast cancer: correlation with response to neoadjuvant chemotherapy and metastasis-free survival [J].
Bertucci, F. ;
Ueno, N. T. ;
Finetti, P. ;
Vermeulen, P. ;
Lucci, A. ;
Robertson, F. M. ;
Marsan, M. ;
Iwamoto, T. ;
Krishnamurthy, S. ;
Masuda, H. ;
Van Dam, P. ;
Woodward, W. A. ;
Cristofanilli, M. ;
Reuben, J. M. ;
Dirix, L. ;
Viens, P. ;
Symmans, W. F. ;
Birnbaum, D. ;
Van Laere, S. J. .
ANNALS OF ONCOLOGY, 2014, 25 (02) :358-365
[3]   Genomic profiling of inflammatory breast cancer: A review [J].
Bertucci, Franois ;
Finetti, Pascal ;
Vermeulen, Peter ;
Van Dam, Peter ;
Dirix, Luc ;
Birnbaum, Daniel ;
Viens, Patrice ;
Van Laere, Steven .
BREAST, 2014, 23 (05) :538-545
[4]   INFLAMMATORY CARCINOMAS OF THE BREAST - A CLINICAL, PATHOLOGICAL, OR A CLINICAL AND PATHOLOGICAL DEFINITION [J].
BONNIER, P ;
CHARPIN, C ;
LEJEUNE, C ;
ROMAIN, S ;
TUBIANA, N ;
BEEDASSY, B ;
MARTIN, PM ;
SERMENT, H ;
PIANA, L .
INTERNATIONAL JOURNAL OF CANCER, 1995, 62 (04) :382-385
[5]   Phase II Study to Evaluate the Efficacy and Safety of Neoadjuvant Lapatinib Plus Paclitaxel in Patients With Inflammatory Breast Cancer [J].
Boussen, Hamouda ;
Cristofanilli, Massimo ;
Zaks, Tal ;
DeSilvio, Michelle ;
Salazar, Vanessa ;
Spector, Neil .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (20) :3248-3255
[6]   Preoperative therapy with trastuzumab and paclitaxel followed by sequential adjuvant doxorubicin/cyclophosphamide for HER2 overexpressing stage II or III breast cancer: A pilot study [J].
Burstein, HJ ;
Harris, LN ;
Gelman, R ;
Lester, SC ;
Nunes, RA ;
Kaelin, CM ;
Parker, LM ;
Ellisen, LW ;
Kuter, I ;
Gadd, MA ;
Christian, RL ;
Kennedy, PR ;
Borges, VF ;
Bunnell, CA ;
Younger, J ;
Smith, BL ;
Winer, EP .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (01) :46-53
[7]   Defining the molecular biology of inflammatory breast cancer [J].
Charafe-Lauffret, Emmanuelle ;
Tarpin, Corole ;
Viens, Patrice ;
Bertucci, Francois .
SEMINARS IN ONCOLOGY, 2008, 35 (01) :41-50
[8]   Histone deacetylase inhibitors modulate miRNA and mRNA expression, block metaphase, and induce apoptosis in inflammatory breast cancer cells [J].
Chatterjee, Namita ;
Wang, Wei-Lin Winnie ;
Conklin, Tucker ;
Chittur, Sridar ;
Tenniswood, Martin .
CANCER BIOLOGY & THERAPY, 2013, 14 (07) :658-671
[9]  
Cristofanilli M, 2001, CANCER-AM CANCER SOC, V92, P1775, DOI 10.1002/1097-0142(20011001)92:7<1775::AID-CNCR1693>3.0.CO
[10]  
2-E