Division of Medical Oncology, Mayo Clinic, 200 First St SW, Rochester, MN, 55905, USA,
Curr Oncol Rep. 2013 Oct;15(5):492-9. doi: 10.1007/s11912-013-0334-4.
Metastatic malignant melanoma is a uniformly fatal disease. Tumor growth and metastasis are associated with angiogenesis and lymphangiogenesis. Proangiogenic factors are associated with higher disease burdens and worse outcomes in melanoma. Accordingly, many agents that target angiogenesis have been studied in melanoma. Angiogenesis is a complex, multifaceted process with many potential therapeutic targets. So far, monoclonal antibodies, immune conjugates, tyrosine kinase inhibitors, immunomodulatory agents, and other therapies have been tested in the phase 2 or phase 3 setting for the treatment of metastatic melanoma. The antiangiogenic agents that have been tested to date offer little activity as single agents, but in combination with cytotoxic agents prolong progression-free survival. We explore data from published phase 2 and phase 3 trials in addition to the purported mechanisms of action of antiangiogenic agents.
转移性恶性黑色素瘤是一种普遍致命的疾病。肿瘤生长和转移与血管生成和淋巴管生成有关。促血管生成因子与黑色素瘤更高的疾病负担和更差的预后相关。因此,许多针对血管生成的药物已在黑色素瘤中进行了研究。血管生成是一个复杂的、多方面的过程,有许多潜在的治疗靶点。到目前为止,单克隆抗体、免疫偶联物、酪氨酸激酶抑制剂、免疫调节剂和其他疗法已在 2 期或 3 期临床试验中用于治疗转移性黑色素瘤。迄今为止,经过测试的抗血管生成药物作为单一药物活性很小,但与细胞毒性药物联合使用可延长无进展生存期。我们探讨了已发表的 2 期和 3 期试验的数据,以及抗血管生成药物的作用机制。