Surgical Breast Centre, Singleton Hospital, Swansea, United Kingdom.
Maturitas. 2011 Feb;68(2):121-8. doi: 10.1016/j.maturitas.2010.10.012. Epub 2010 Dec 8.
Breast cancer is the most common cancer among women in the UK, with 46,000 new cases and 12,000 deaths due to this disease estimated to have occurred in 2008. Around three-quarters of breast cancers express the estrogen receptor and are therefore presumed to be hormone-responsive and potentially treatable or preventable by anti-estrogenic agents. Expression of the HER2 receptor occurs in a fifth of breast cancers and is associated with limited endocrine response in hormone receptor-positive tumours and directs treatment with HER2-targeted agents. Despite improvements in the clinical outcome of breast cancer patients through the development of endocrine and targeted agents, overcoming de novo or acquired resistance remains a considerable therapeutic hurdle. In addition, as our understanding of the complexity of breast cancer biology increases, it is clear that existing therapies will fall short of offering an effective treatment solution to many patients. The ability to profile molecular pathways in drug-responsive and drug-resistant tumours has provided an important step in identifying novel targets in breast cancer. To this end, a number of new targeted therapeutics are currently being investigated both as single agents and as a means to improve existing therapeutic regimens.
在英国,乳腺癌是女性最常见的癌症,据估计,2008 年有 4.6 万例新发病例和 1.2 万例死亡归因于该病。大约四分之三的乳腺癌表达雌激素受体,因此被认为是激素反应性的,并且可以通过抗雌激素药物进行治疗或预防。HER2 受体的表达发生在五分之一的乳腺癌中,并且与激素受体阳性肿瘤中的内分泌反应有限相关,并指导使用 HER2 靶向药物进行治疗。尽管通过开发内分泌和靶向药物改善了乳腺癌患者的临床结局,但克服新出现的或获得性耐药仍然是一个相当大的治疗障碍。此外,随着我们对乳腺癌生物学复杂性的理解的增加,很明显,现有的治疗方法将无法为许多患者提供有效的治疗解决方案。在有反应的肿瘤和耐药肿瘤中对分子途径进行分析的能力为确定乳腺癌中的新靶标提供了重要的一步。为此,目前正在作为单一药物和作为改善现有治疗方案的手段来研究许多新的靶向治疗药物。