Pal Sumanta Kumar, Mortimer Joanne
Division of Genitourinary Malignancies, Department of Medical Oncology & Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA 91010, USA.
Maturitas. 2009 Aug 20;63(4):269-74. doi: 10.1016/j.maturitas.2009.06.010. Epub 2009 Jul 25.
Triple-negative breast cancer (TNBC) accounts for approximately 15% of breast cancer diagnoses, and exhibits substantial overlap with basal-type and BRCA1-positive breast cancer. In recent years, a greater understanding of the biology of this disease has led to the development of numerous and varied therapeutic approaches. Neoadjuvant trials using conventional cytotoxic agents such as cisplatin have demonstrated TNBC to be a relatively chemo-sensitive disease. In the current review, focus is directed towards novel targeted strategies for TNBC. Recent trials have shown the poly(ADP-ribosyl)ation polymerase (PARP) inhibitors BSI-201 and olaparib to be highly effective in TNBC and BRCA1/2-positive disease, respectively. Efforts to assess the role of antiangiogenic agents such as bevacizumab and sunitinib in TNBC are ongoing. Finally, preclinical studies provide a signal of potential activity with use of heat shock protein 90 (Hsp90) and Src inhibitors in this breast cancer subtype.
三阴性乳腺癌(TNBC)约占乳腺癌诊断病例的15%,并且与基底样型和BRCA1阳性乳腺癌有很大重叠。近年来,对这种疾病生物学特性的深入了解促使了多种治疗方法的发展。使用顺铂等传统细胞毒性药物的新辅助试验表明TNBC是一种相对化疗敏感的疾病。在当前的综述中,重点关注TNBC的新型靶向策略。最近的试验显示,聚(ADP - 核糖基)化聚合酶(PARP)抑制剂BSI - 201和奥拉帕尼分别在TNBC和BRCA1/2阳性疾病中具有高效性。评估贝伐单抗和舒尼替尼等抗血管生成药物在TNBC中的作用的研究正在进行。最后,临床前研究显示在这种乳腺癌亚型中使用热休克蛋白90(Hsp90)和Src抑制剂有潜在活性迹象。