CI Parhon National Institute of Endocrinology, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Northwest Pituitary Center, and Departments of Medicine (Endocrinology) and Neurological Surgery, Oregon Health & Science University, Portland, United States.
Horm Metab Res. 2020 Jan;52(1):8-24. doi: 10.1055/a-1066-4592. Epub 2019 Dec 20.
Pituitary adenomas represent approximately 15% of brain tumors; incidence is significantly on the increase due to widespread use of magnetic resonance imaging. Surgery remains the first-line treatment for most tumors overall. The role of dopaminergic agonists (DAs) and somatostatin receptor ligands (SRLs) in the treatment of pituitary adenomas is quite well established for prolactinomas and growth hormone (GH) excess. However, over the last decade new multi-receptor binding SRLs are increasingly used for treatment of acromegaly and Cushing's disease. SRLs/DA chimeric compounds seem to have enhanced potency and efficacy when compared to that of individual SRLs or DA receptor agonists according to preclinical data. However, following negative results, more research is needed to determine if this interesting mechanism will translate into positive clinical effects for acromegaly patients. Furthermore, new agents that block adrenal steroidogenesis have been developed in phase III clinical trials for Cushing's disease and several new compounds working at the pituitary level and/or blocking the glucocorticoid receptor are also in development. Combination therapy of drugs with similar or different mechanisms (possibly synergistic) are also on the increase. A growing awareness regarding all mechanisms involved in both control of pituitary secretion and cellular proliferation might allow for sole medical treatment of pituitary adenomas, especially macroadenomas, rather than surgery and/or radiation therapy, in the future. Moreover, the underlying decision on how to treat patients with pituitary adenomas should be individualized on a case-by-case basis with not only a goal of tumor shrinkage and biochemical control, but also of improving patients' quality of life.
垂体腺瘤占脑肿瘤的 15%左右;由于磁共振成像的广泛应用,其发病率显著增加。手术仍然是大多数肿瘤的首选治疗方法。多巴胺激动剂(DA)和生长抑素受体配体(SRL)在催乳素瘤和生长激素(GH)过度分泌的治疗中作用已经得到充分证实。然而,在过去十年中,新型多受体结合 SRL 越来越多地用于治疗肢端肥大症和库欣病。根据临床前数据,SRL/DA 嵌合化合物与单独的 SRL 或 DA 受体激动剂相比,似乎具有增强的效力和疗效。然而,在得到阴性结果后,需要进行更多的研究来确定这种有趣的机制是否会对肢端肥大症患者产生积极的临床效果。此外,用于库欣病的阻断肾上腺类固醇生成的新药物已经在 III 期临床试验中开发,并且还有几种在垂体水平起作用和/或阻断糖皮质激素受体的新型化合物也正在开发中。具有相似或不同机制(可能具有协同作用)的药物联合治疗也在增加。对控制垂体分泌和细胞增殖的所有机制的认识不断提高,可能允许仅通过药物治疗来治疗垂体腺瘤,尤其是大腺瘤,而不是手术和/或放射治疗,在未来。此外,如何治疗垂体腺瘤患者的决策应该根据具体情况个体化,不仅要达到肿瘤缩小和生化控制的目标,还要提高患者的生活质量。