Bartsch Rupert, Bergen Elisabeth
1Department of Medicine 1, Clinical Division of Oncology, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.
2Comprehensive Cancer Center Vienna, Medical University of Vienna, Vienna, Austria.
Memo. 2018;11(4):280-283. doi: 10.1007/s12254-018-0441-x. Epub 2018 Oct 11.
At the 2018 ASCO Annual Meeting, data from several interesting studies in HER2-positive metastatic breast cancer were presented. While not immediately practice changing, these trials indicate the future directions of drug development in this field. Early phase studies with novel antibody-drug conjugates (ADCs) such as trastuzumab-deruxtecan and trastuzumab-duocarmazine suggest relevant clinical activity of these drugs in pretreated patients; in addition, these ADCs may offer activity in low HER2-expressing tumours as well. ZW25, a bispecific HER2-directed antibody targeting the extracellular domains 2 and 4, showed excellent tolerability and considerable single-agent activity. A combination of T‑DM1 with the tyrosine-kinase inhibitor neratinib yielded high response rates, while a study of trastuzumab plus durvalumab reported disappointing results. Although formally negative, overall survival data from the PHEREXA trial suggest clinical activity of dual HER2-inhibition with trastuzumab and pertuzumab in patients with prior trastuzumab treatment for advanced disease. A combined analysis of two tucatinib studies showed that systemic therapy is active when continued in case of isolated central nervous system progression and stable extracranial disease after local therapy of brain metastases; finally, a small prospective observation in asymptomatic patients with reduced left ventricular ejection fraction suggests that anti-HER2 treatment may be reasonably safe in this population.
在2018年美国临床肿瘤学会(ASCO)年会上,公布了几项关于HER2阳性转移性乳腺癌的有趣研究数据。虽然这些试验不会立即改变临床实践,但它们指明了该领域药物研发的未来方向。早期针对新型抗体药物偶联物(ADC)的研究,如曲妥珠单抗-德卢替康和曲妥珠单抗-多卡马嗪,表明这些药物在经治患者中具有相关临床活性;此外,这些ADC在低HER2表达肿瘤中也可能具有活性。ZW25是一种靶向细胞外结构域2和4的双特异性HER2导向抗体,显示出优异的耐受性和可观的单药活性。曲妥珠单抗-美坦新(T-DM1)与酪氨酸激酶抑制剂来那替尼联合使用产生了高缓解率;而一项关于曲妥珠单抗联合度伐利尤单抗的研究报告了令人失望的结果。尽管PHEREXA试验的总生存数据形式上为阴性,但表明对于先前接受曲妥珠单抗治疗的晚期疾病患者,曲妥珠单抗和帕妥珠单抗双重HER2抑制具有临床活性。两项图卡替尼研究的综合分析表明,在脑转移瘤局部治疗后出现孤立的中枢神经系统进展且颅外疾病稳定的情况下继续进行全身治疗是有效的;最后,一项针对左心室射血分数降低的无症状患者的小型前瞻性观察表明,抗HER2治疗在该人群中可能相当安全。