Mukherjee A, Dhadda A S, Shehata M, Chan Stephen
Nottingham University Hospitals NHS Trust (City Hospital Campus), Department of Clinical Oncology, Nottingham, UK.
Expert Opin Pharmacother. 2007 Sep;8(13):2189-204. doi: 10.1517/14656566.8.13.2189.
Lapatinib is a dual (ErbB-1 and ErB-2) receptor tyrosine kinase inhibitor (TKI) that was recently approved by the FDA for the treatment of advanced breast cancer. It shows synergy with trastuzumab, and has demonstrated clinical activity in trastuzumab-resistant tumour. This paper reviews the drug development of lapatinib from preclinical studies to the pivotal Phase III trial and ongoing clinical studies. Areas of interest include the advantages of small molecule TKIs versus antibodies in targeting HER receptors and the efficacy of lapatinib in the treatment of cerebral metastases. The surprisingly high response rate in inflammatory breast cancer raises the possibility of other novel predictive biomarkers. The potential for combination and sequencing with other biological and cytotoxic agents is both exciting and challenging.
拉帕替尼是一种双靶点(ErbB-1和ErbB-2)受体酪氨酸激酶抑制剂(TKI),最近被美国食品药品监督管理局(FDA)批准用于治疗晚期乳腺癌。它与曲妥珠单抗具有协同作用,并已在曲妥珠单抗耐药的肿瘤中显示出临床活性。本文回顾了拉帕替尼从临床前研究到关键的III期试验以及正在进行的临床研究的药物研发过程。感兴趣的领域包括小分子TKI与抗体在靶向HER受体方面的优势以及拉帕替尼治疗脑转移瘤的疗效。炎性乳腺癌中令人惊讶的高缓解率增加了其他新型预测生物标志物的可能性。与其他生物制剂和细胞毒性药物联合使用及序贯使用的潜力既令人兴奋又具有挑战性。