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功能性垂体腺瘤——当前的治疗选择与新兴药物疗法

Functioning Pituitary Adenomas - Current Treatment Options and Emerging Medical Therapies.

作者信息

Varlamov Elena V, McCartney Shirley, Fleseriu Maria

机构信息

Oregon Health & Science University, Oregon, USA.

出版信息

Eur Endocrinol. 2019 Apr;15(1):30-40. doi: 10.17925/EE.2019.15.1.30. Epub 2019 Apr 12.

DOI:10.17925/EE.2019.15.1.30
PMID:31244908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6587904/
Abstract

Pituitary adenomas are benign tumours comprising approximately 16% of all primary cranial neoplasms. Functioning pituitary adenomas (prolactinomas, somatotroph, corticotroph, thyrotroph and rarely gonadotroph adenomas) cause complex clinical syndromes and require prompt treatment to reduce associated morbidity and mortality. Treatment approaches include transsphenoidal surgery, medical therapy and radiation. Medical therapy is the primary therapy for prolactinomas, and surgery by a skilled neurosurgeon is the first-line approach for other functioning pituitary adenomas. A multimodal treatment is frequently necessary to achieve biochemical and clinical control, especially, when surgery is not curative or when medical therapy fails. Several emerging, novel, medical treatments for acromegaly, Cushing's disease and prolactinomas are in phase II and III clinical trials and may become effective additions to the current drug armamentarium. The availability of various management options will allow an individualised treatment approach based on the unique tumour type, clinical situation and patient preference.

摘要

垂体腺瘤是良性肿瘤,约占所有原发性颅脑肿瘤的16%。功能性垂体腺瘤(泌乳素瘤、生长激素瘤、促肾上腺皮质激素瘤、促甲状腺激素瘤以及罕见的促性腺激素瘤)会引发复杂的临床综合征,需要及时治疗以降低相关的发病率和死亡率。治疗方法包括经蝶窦手术、药物治疗和放射治疗。药物治疗是泌乳素瘤的主要治疗方法,而由经验丰富的神经外科医生进行的手术则是其他功能性垂体腺瘤的一线治疗方法。为实现生化和临床控制,通常需要采取多模式治疗,尤其是在手术无法治愈或药物治疗失败的情况下。几种针对肢端肥大症、库欣病和泌乳素瘤的新兴、新型药物治疗正处于II期和III期临床试验阶段,可能会成为当前药物库中的有效补充。多种治疗选择的可用性将使基于独特肿瘤类型、临床情况和患者偏好的个体化治疗方法成为可能。

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本文引用的文献

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Systemic Complications of Acromegaly and the Impact of the Current Treatment Landscape: An Update.肢端肥大症的全身并发症及当前治疗现状的影响:最新进展。
Endocr Rev. 2019 Feb 1;40(1):268-332. doi: 10.1210/er.2018-00115.
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Identification of recurrent USP48 and BRAF mutations in Cushing's disease.鉴定库欣病中 USP48 和 BRAF 的复发性突变。
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PATHOGENESIS OF CUSHING DISEASE: AN UPDATE ON THE GENETICS OF CORTICOTROPINOMAS.库欣病的发病机制:促肾上腺皮质细胞瘤遗传学的最新研究进展。
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Efficacy and Safety of switching to Pasireotide in Acromegaly Patients controlled with Pegvisomant and Somatostatin Analogues: PAPE extension study.培维索孟和生长抑素类似物治疗控制下的肢端肥大症患者切换为帕瑞肽的疗效和安全性:PAPE 扩展研究。
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