Developmental therapeutics for inflammatory breast cancer: Biology and translational directions

被引:18
作者
Costa, Ricardo [1 ]
Santa-Maria, Cesar A. [1 ,2 ]
Rossi, Giovanna [2 ]
Carneiro, Benedito A. [1 ,2 ]
Chae, Young Kwang [1 ,2 ]
Gradishar, William J. [1 ,2 ]
Giles, Francis J. [1 ,2 ]
Cristofanilli, Massimo [1 ,2 ]
机构
[1] Feinberg Sch Med, Div Hematol Oncol, Dev Therapeut Program, Chicago, IL 60611 USA
[2] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
关键词
inflammatory breast cancer; targeted therapy; immunotherapy; CONTROLLED SUPERIORITY TRIAL; PERTUZUMAB PLUS TRASTUZUMAB; GROUP PROTEIN EZH2; GROWTH-FACTOR; PHASE-II; NEOADJUVANT CHEMOTHERAPY; PATHOLOGICAL RESPONSE; GENE-EXPRESSION; RHOC GTPASE; DOXORUBICIN-CYCLOPHOSPHAMIDE;
D O I
10.18632/oncotarget.13778
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Inflammatory breast cancer (IBC) is a rare and aggressive form of breast cancer, which accounts for approximately 3% of cases of breast malignancies. Diagnosis relies largely on its clinical presentation, and despite a characteristic phenotype, underlying molecular mechanisms are poorly understood. Unique clinical presentation indicates that IBC is a distinct clinical and biological entity when compared to nonIBC. Biological understanding of non-IBC has been extrapolated into IBC and targeted therapies for HER2 positive (HER2+) and hormonal receptor positive non-IBC led to improved patient outcomes in the recent years. This manuscript reviews recent discoveries related to the underlying biology of IBC, clinical progress to date and suggests rational approaches for investigational therapies.
引用
收藏
页码:12417 / 12432
页数:16
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