Breast Center, Department Obstetrics & Gynecology & CCC LMU, University of Munich, Marchioninistrasse 15, 81377 Munich, Germany.
Future Oncol. 2014 Jan;10(1):21-40. doi: 10.2217/fon.13.244.
Aberrant signaling of the ErbB family of receptors plays an integral role in the tumorigenesis of many cancer types, including head and neck squamous cell carcinoma (HNSCC) and breast cancer (BC). Significant research efforts have focused on developing new treatments that target ErbB family members, with the last decade seeing the approval of small-molecule tyrosine kinase inhibitors and monoclonal antibodies that inhibit ErbB signaling. However, treatment resistance is an ever-growing problem and, therefore, new therapies are being investigated to overcome this hurdle. Afatinib is an irreversible ErbB family blocker that has demonstrated potent anti-tumor activity in preclinical models and has displayed clinical efficacy in patients with non-small-cell lung cancer, and activity in HNSCC and BC. Here, the preclinical and clinical development of afatinib in the treatment of non-small-cell lung cancer, HNSCC and BC is described in the context of currently approved agents.
ErbB 家族受体的异常信号转导在多种癌症类型的肿瘤发生中起着重要作用,包括头颈部鳞状细胞癌 (HNSCC) 和乳腺癌 (BC)。大量研究集中于开发针对 ErbB 家族成员的新治疗方法,过去十年见证了小分子酪氨酸激酶抑制剂和单克隆抗体的批准,这些药物可抑制 ErbB 信号转导。然而,治疗耐药性是一个日益严重的问题,因此正在研究新的疗法来克服这一障碍。阿法替尼是一种不可逆的 ErbB 家族阻滞剂,在临床前模型中显示出强大的抗肿瘤活性,并在非小细胞肺癌患者中显示出临床疗效,以及在 HNSCC 和 BC 中的活性。本文描述了阿法替尼在治疗非小细胞肺癌、HNSCC 和 BC 中的临床前和临床开发情况,并结合了目前已批准的药物。