Department of Oncology and Hematology, Division of Oncology, University Hospital Modena, Modena, Italy.
School of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Expert Opin Investig Drugs. 2021 Apr;30(4):411-418. doi: 10.1080/13543784.2021.1881479. Epub 2021 Mar 28.
: Biliary Tract Cancer (BTC) is a heterogeneous group of malignant neoplasms with a complex molecular pathogenesis. The prognosis of metastatic disease is dramatically dismal and therapeutic options are scarce. Systemic chemotherapy is the gold standard for the metastatic disease. However, because of the disappointing results with conventional chemotherapy, investigators have turned to new biological therapeutic options targeting the main molecular pathways, neo-angiogenesis, involved in the disease pathogenesis.: This paper examines the rationale of using antiangiogenic therapies in this setting, evaluates the therapeutic implications, and highlights ongoing studies and future perspectives. A Pubmed systematic review of preclinical and clinical data was performed which enabled the composition of this paper.: Amore in-depth understanding of the interplay between the neo-angiogenesis pathways, and the microenvironment will could propel the design new therapeutic strategies. Nowadays, the combination of antiangiogenic drugs and immune check-point inhibitors looks promising, but further, more comprehensive data are necessary to gain afuller picture. In an era of novel technologies and techniques, which includes radiomics, the challenge is to identify the biomarkers of response to antiangiogenic drugs which will permit the selection of patients that are more likely to respond to antiangiogenic therapies.
胆管癌(BTC)是一组具有复杂分子发病机制的异质性恶性肿瘤。转移性疾病的预后非常差,治疗选择有限。系统化疗是转移性疾病的金标准。然而,由于常规化疗的结果令人失望,研究人员已经转向针对疾病发病机制中涉及的主要分子途径(新生血管生成)的新型生物治疗选择。本文研究了在这种情况下使用抗血管生成治疗的基本原理,评估了治疗意义,并强调了正在进行的研究和未来的展望。对临床前和临床数据进行了 Pubmed 系统评价,在此基础上撰写了本文。更深入地了解新生血管生成途径与微环境之间的相互作用,可以推动设计新的治疗策略。如今,抗血管生成药物与免疫检查点抑制剂的联合应用前景看好,但还需要更多全面的数据来获得更全面的认识。在包括放射组学在内的新技术和新方法时代,面临的挑战是确定对抗血管生成药物反应的生物标志物,从而选择更有可能对抗血管生成治疗产生反应的患者。