Eleutherakis-Papaiakovou V, Karali M, Kokkonouzis I, Tiliakos I, Dimopoulos M A
Department of Clinical Therapeutics, University of Athens School of Medicine, Athens, Greece.
Leuk Lymphoma. 2003 Jun;44(6):937-48. doi: 10.1080/1042819031000067639.
It is now well established that solid tumors depend on angiogenesis. Promoters and inhibitors of angiogenesis are in balance and antiangiogenic strategies aim at repressing the angiogenic process, thus retarding solid tumor progression. Recent data suggest the importance of angiogenesis in hematologic malignancies and several studies reveal an increased angiogenesis in active multiple myeloma. Angiogenesis seems to be a prominent feature of MM progression, and seems to be correlated with the prognosis and the resistance of MM to chemotherapy. Numerous cell populations and cytokines are involved in angiogenesis in multiple myeloma and antiangiogenic therapy with thalidomide is effective in patients with refractory or relapsed disease. The combination of thalidomide and of other immunomodulatory agents with other therapeutic regimens could lead to more effective management of patients with multiple myeloma.
现已充分证实实体瘤依赖于血管生成。血管生成的促进剂和抑制剂处于平衡状态,抗血管生成策略旨在抑制血管生成过程,从而延缓实体瘤进展。近期数据表明血管生成在血液系统恶性肿瘤中具有重要性,多项研究显示活动性多发性骨髓瘤中血管生成增加。血管生成似乎是多发性骨髓瘤进展的一个突出特征,并且似乎与多发性骨髓瘤的预后及化疗耐药性相关。多种细胞群体和细胞因子参与多发性骨髓瘤的血管生成,沙利度胺抗血管生成治疗对难治性或复发性疾病患者有效。沙利度胺与其他免疫调节剂以及其他治疗方案联合应用可能会更有效地治疗多发性骨髓瘤患者。