Alonso-Gordoa T, Capdevila J, Grande E
Medical Oncology DepartmentRamón y Cajal University Hospital, Carretera de Colmenar Km 9,100, 28034 Madrid, SpainMedical Oncology DepartmentVall d'Hebrón University Hospital, Passeig de la Vall d'Hebrón, 119-129, 08035 Barcelona, Spain.
Medical Oncology DepartmentRamón y Cajal University Hospital, Carretera de Colmenar Km 9,100, 28034 Madrid, SpainMedical Oncology DepartmentVall d'Hebrón University Hospital, Passeig de la Vall d'Hebrón, 119-129, 08035 Barcelona, Spain
Eur J Endocrinol. 2015 Jan;172(1):R31-46. doi: 10.1530/EJE-14-0354.
Neuroendocrine tumours (NETs) represent a less frequent and heterogeneous group of tumours, which has experienced, in recent years, a significant increase in effective therapeutic possibilities overcoming the disappointing results from chemotherapy. Initial improvements in treatment strategies came from somatostatin analogues (SSAs) that have widely demonstrated a significant improvement in symptomatic relief and tumour control growth by a complex mechanism of action over cell survival, angiogenesis and immunomodulation. Recent investigations have pointed out novel SSAs with a wider binding profile (pasireotide), chimeric molecules against somatostatin receptors and dopamine receptors and the combination with targeted agents, such as mTOR inhibitors or antiangiogenic agents. Immunotherapy is the second cornerstone in NET treatment and has been represented with interferon alpha for a long time, with a demonstrated activity on tumour and clinical response. Its less manageable adverse events have limited its usage. However, different checkpoints in immune system regulation have been effectively targeted in different solid tumours, and novel approaches are currently arising in NETs. In conclusion, biotherapy remains an active treatment strategy for initial approach in patients with NETs. Further investigation on patients' selection, molecular profiles, treatment sequence or combination and optimisation of current and novel biotherapy agents is required.
神经内分泌肿瘤(NETs)是一类较为少见且异质性的肿瘤,近年来,其有效治疗可能性显著增加,克服了化疗令人失望的结果。治疗策略的初步改进来自生长抑素类似物(SSAs),通过对细胞存活、血管生成和免疫调节的复杂作用机制,SSAs已广泛证明在缓解症状和控制肿瘤生长方面有显著改善。最近的研究指出了具有更广泛结合谱的新型SSAs(帕瑞肽)、针对生长抑素受体和多巴胺受体的嵌合分子以及与靶向药物(如mTOR抑制剂或抗血管生成药物)的联合应用。免疫疗法是NET治疗的第二个基石,长期以来一直以干扰素α为代表,对肿瘤和临床反应有明确的活性。其较难处理的不良事件限制了其使用。然而,免疫系统调节中的不同检查点已在不同实体瘤中得到有效靶向,目前NETs中也出现了新的方法。总之,生物疗法仍然是NET患者初始治疗的积极策略。需要对患者选择、分子特征、治疗顺序或联合应用以及当前和新型生物治疗药物的优化进行进一步研究。