Oki Yutaka
Department of Family and Community Medicine, Hamamatsu University School of Medicine.
Neurol Med Chir (Tokyo). 2014;54(12):958-65. doi: 10.2176/nmc.ra.2014-0239. Epub 2014 Nov 29.
The treatment of functioning pituitary adenoma (FPA) must achieve endocrinological remission as well as tumor size reduction. The first-line treatment of FPA except prolactinoma is transsphenoidal surgery (TSS). Medical treatments and/or radiation will be applied as adjuvant therapies succeeding to TSS. In patients with prolactinoma, dopamine agonists, especially cabergoline, are quite efficient. Dopamine agonists decrease plasma prolactin levels and induce shrinkage in most patients and can be ceased in some of them. In patients with acromegaly, dopamine agonists, somatostatin analogues, and growth hormone receptor antagonist have been used as a monotherapy or the combination, and the high remission rate can be achieved. Pasireotide having high affinity to type 5 somatostatin receptors will be available for the patients presenting resistance against type 2 receptor agonists, such as octreotide and lanreotide. The preceding treatment with somatostatin analogues is beneficial for improving the success rate of TSS. The chimera compounds of somatostatin analogues and dopamine agonists have been investigated. The medical treatments of Cushing's disease are challenging, if TSS is not successful. To suppress ACTH secretion, dopamine agonists and somatostatin analogues have been examined, but neither came to show a sufficient effect. Pasireotide reduces urinary cortisol excretion with a high remission rate. Adrenal enzyme inhibitors (AEIs), such as metyrapone, can inhibit cortisol synthesis form adrenal glands promptly and sufficiently in most of patients. LCI699, a newly developed AEI, is more potent than metyrapone and will be available. We should use available medical treatments for improving the prognosis and quality of life.
功能性垂体腺瘤(FPA)的治疗必须实现内分泌缓解以及肿瘤体积缩小。除泌乳素瘤外,FPA的一线治疗方法是经蝶窦手术(TSS)。TSS后将采用药物治疗和/或放疗作为辅助治疗。对于泌乳素瘤患者,多巴胺激动剂,尤其是卡麦角林,疗效显著。多巴胺激动剂可降低血浆催乳素水平,使大多数患者的肿瘤缩小,部分患者还可停药。对于肢端肥大症患者,多巴胺激动剂、生长抑素类似物和生长激素受体拮抗剂已被用作单一疗法或联合疗法,且可实现较高的缓解率。对奥曲肽和兰瑞肽等2型受体激动剂耐药的患者,可使用对5型生长抑素受体具有高亲和力的帕瑞肽。术前使用生长抑素类似物有助于提高TSS的成功率。生长抑素类似物和多巴胺激动剂的嵌合化合物已在研究中。如果TSS不成功,库欣病的药物治疗具有挑战性。为抑制促肾上腺皮质激素(ACTH)分泌,已对多巴胺激动剂和生长抑素类似物进行了研究,但均未显示出足够的效果。帕瑞肽可降低尿皮质醇排泄,缓解率较高。肾上腺酶抑制剂(AEIs),如甲吡酮,可在大多数患者中迅速且充分地抑制肾上腺皮质醇合成。新开发的AEI LCI699比甲吡酮更有效,即将上市。我们应使用现有的药物治疗来改善预后和生活质量。