Beck J Thaddeus
Highlands Oncology Group, Fayetteville, AR, USA.
Onco Targets Ther. 2015 Dec 7;8:3629-38. doi: 10.2147/OTT.S88037. eCollection 2015.
Despite advances in cytotoxic chemotherapy and targeted therapies, 5-year survival rates remain low for patients with advanced breast cancer at diagnosis. This highlights the limited effectiveness of current treatment options. An improved understanding of cellular functions associated with the development and progression of breast cancer has resulted in the creation of a number of novel targeted molecular therapies. However, more work is needed to improve outcomes, particularly in the first-line recurrent or metastatic hormone receptor-positive breast cancer setting. The phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin (mTOR) pathway is a major intracellular signaling pathway that is often upregulated in breast cancer, and overactivation of this pathway has been associated with primary or developed resistance to endocrine treatment. Clinical data from the Phase III Breast Cancer Trials of Oral Everolimus-2 (BOLERO-2) study of the mTOR inhibitor everolimus combined with exemestane in hormone receptor-positive advanced breast cancer were very promising, highlighting the potential role of mTOR inhibitors in combination with endocrine therapies as a first-line treatment option for these patients. It is hoped that the use of mTOR inhibitors combined with current standard-of-care endocrine therapies, such as aromatase inhibitors, in the first-line advanced breast cancer setting may result in greater antitumor effects and also delay or reverse treatment resistance.
尽管细胞毒性化疗和靶向治疗取得了进展,但晚期乳腺癌患者在诊断时的5年生存率仍然很低。这凸显了当前治疗方案的有效性有限。对与乳腺癌发生和进展相关的细胞功能的进一步了解,催生了许多新型靶向分子疗法。然而,仍需要更多工作来改善治疗结果,尤其是在一线复发或转移性激素受体阳性乳腺癌的情况下。磷脂酰肌醇3激酶/蛋白激酶B/雷帕霉素哺乳动物靶点(mTOR)通路是一条主要的细胞内信号通路,在乳腺癌中常被上调,该通路的过度激活与对内分泌治疗的原发性或获得性耐药有关。mTOR抑制剂依维莫司与依西美坦联合用于激素受体阳性晚期乳腺癌的口服依维莫司-2(BOLERO-2)III期乳腺癌试验的临床数据非常有前景,凸显了mTOR抑制剂与内分泌疗法联合作为这些患者一线治疗选择的潜在作用。人们希望,在一线晚期乳腺癌治疗中使用mTOR抑制剂与当前标准护理内分泌疗法(如芳香化酶抑制剂)联合,可能会产生更大的抗肿瘤效果,并延缓或逆转治疗耐药性。