D'Aniello Carmine, Berretta Massimiliano, Cavaliere Carla, Rossetti Sabrina, Facchini Bianca Arianna, Iovane Gelsomina, Mollo Giovanna, Capasso Mariagrazia, Pepa Chiara Della, Pesce Laura, D'Errico Davide, Buonerba Carlo, Di Lorenzo Giuseppe, Pisconti Salvatore, De Vita Ferdinando, Facchini Gaetano
Division of Medical Oncology, A.O.R.N. dei COLLI "Ospedali Monaldi-Cotugno-CTO," Naples, Italy.
Division of Medical Oncology, Istituto Nazionale Tumori, IRCCS CRO Aviano (PN), Milan, Italy.
Front Oncol. 2019 Dec 11;9:1400. doi: 10.3389/fonc.2019.01400. eCollection 2019.
In the last decades, the prognosis of metastatic renal cell carcinoma (mRCC) has remarkably improved following the advent of the "targeted therapy" era. The expanding knowledge on the prominent role played by angiogenesis in RCC pathogenesis has led to approval of multiple anti-angiogenic agents such as sunitinib, pazopanib, axitinib, cabozantinib, sorafenib, and bevacizumab. These agents can induce radiological responses and delay cancer progression for months or years before onset of resistance, with a clinically meaningful activity. The need for markers of prognosis and efficacy of anti-angiogenic agents has become more compelling as novel systemic immunotherapy agents have also been approved in RCC and can be administered as an alternative to angiogenesis inhibitors. Anti PD-1 monoclonal antibody nivolumab has been approved in the second-line setting after tyrosine kinase inhibitors failure, while combination of nivolumab plus anti CTLA-4 monoclonal antibody ipilimumab has been approved as first-line therapy of RCC patients at intermediate or poor prognosis. In this review article, biomarkers of prognosis and efficacy of antiangiogenic therapies are summarized with a focus on those that have the potential to affect treatment decision-making in RCC. Biomarkers predictive of toxicity of anti-angiogenic agents have also been discussed.
在过去几十年中,随着“靶向治疗”时代的到来,转移性肾细胞癌(mRCC)的预后有了显著改善。对血管生成在RCC发病机制中所起重要作用的认识不断深入,促使多种抗血管生成药物获批,如舒尼替尼、帕唑帕尼、阿昔替尼、卡博替尼、索拉非尼和贝伐单抗。这些药物可诱导影像学反应,并在出现耐药之前将癌症进展延迟数月或数年,具有临床意义的活性。随着新型全身免疫治疗药物也在RCC中获批,并可作为血管生成抑制剂的替代药物使用,对抗血管生成药物的预后和疗效标志物的需求变得更加迫切。抗PD - 1单克隆抗体纳武单抗在酪氨酸激酶抑制剂治疗失败后的二线治疗中获批,而纳武单抗联合抗CTLA - 4单克隆抗体伊匹木单抗已获批用于中危或低危RCC患者的一线治疗。在这篇综述文章中,总结了抗血管生成治疗的预后和疗效生物标志物,重点关注那些有可能影响RCC治疗决策的生物标志物。还讨论了抗血管生成药物毒性的预测生物标志物。