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Angiogenesis and anti-angiogenic therapy in prostate cancer

机译:前列腺癌的血管生成和抗血管生成治疗

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Inhibition of angiogenic pathways has proven an effective strategy for the treatment of several common solid tumors however its role in the management of prostate cancer is yet to be defined. Advances in clinical research have resulted in five new treatments for metastatic prostate cancer in the last two years. The immunotherapy sipuleucel-T, the cytotoxic cabazitaxel, the androgen biosynthesis inhibitor abiraterone acetate, the radioisotope radium-223 and the antiandrogen enzalutamide have all been shown to improve overall survival in randomized phase III studies treatment paradigms are changing rapidly. Angiogenesis is known to play a central role in the progression of advanced prostate cancer however established antiangiogenic therapies including bevacizumab and sunitinib have failed to improve survival in randomized trials to date. Novel treatment combinations and novel agents such as cabozantinib are showing promising early results and it is hoped that further well-designed studies will validate the strong biological hypothesis for the benefit of antiangiogenic therapy to improve outcomes for patients with prostate cancer.
机译:血管生成途径的抑制已被证明是治疗几种常见实体瘤的有效策略,但是其在前列腺癌管理中的作用尚待确定。在过去的两年中,临床研究的进展导致了五种治疗转移性前列腺癌的新疗法。免疫疗法sipuleucel-T,细胞毒性卡巴他赛,雄激素生物合成抑制剂醋酸阿比特龙,放射性同位素镭223和抗雄激素enzalutamide均能改善随机III期研究治疗方案的总体生存率。众所周知,血管生成在晚期前列腺癌的进展中起着中心作用,但是迄今为止,包括贝伐单抗和舒尼替尼在内的已确立的抗血管生成疗法在随机试验中均未能提高生存率。新型治疗组合和新型药物(例如卡博替尼)显示出令人鼓舞的早期结果,并希望进一步精心设计的研究能够验证强大的生物学假设,从而有益于抗血管生成治疗,以改善前列腺癌患者的预后。

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