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肢端肥大症预后因素的最新进展:能否建立风险评分?

Update on prognostic factors in acromegaly: Is a risk score possible?

作者信息

Fernandez-Rodriguez E, Casanueva F F, Bernabeu I

机构信息

Endocrinology Division, Servicio Gallego de Salud (SERGAS), Complejo Hospitalario Universitario de Santiago de Compostela, 15706, Santiago de Compostela, La Coruña, Spain.

出版信息

Pituitary. 2015 Jun;18(3):431-40. doi: 10.1007/s11102-014-0574-9.

DOI:10.1007/s11102-014-0574-9
PMID:24858722
Abstract

Certain clinical conditions and markers have recently been demonstrated to modify the natural history of acromegaly in affected patients. Thus, some clinical, histological, radiological and molecular factors are associated with more aggressive pituitary tumors that have higher biochemical activity, higher tumor volumes and decreased tumoral and biochemical responses to current therapies. However, these factors do not seem to have an equal influence on the prognosis of patients with acromegaly. We present a review of the factors that influence the clinical course of patients with acromegaly and propose a risk value for each factor that will allow prognostic scoring for affected patients by considering a combination of these factors.

摘要

最近已证实某些临床状况和标志物可改变肢端肥大症患者的自然病程。因此,一些临床、组织学、放射学和分子因素与侵袭性更强的垂体瘤相关,这些垂体瘤具有更高的生化活性、更大的肿瘤体积,并且对当前治疗的肿瘤和生化反应降低。然而,这些因素对肢端肥大症患者预后的影响似乎并不相同。我们综述了影响肢端肥大症患者临床病程的因素,并针对每个因素提出一个风险值,通过综合考虑这些因素,可为受影响患者进行预后评分。

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Update on prognostic factors in acromegaly: Is a risk score possible?肢端肥大症预后因素的最新进展:能否建立风险评分?
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本文引用的文献

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Pasireotide versus octreotide in acromegaly: a head-to-head superiority study.培高利特与奥曲肽治疗肢端肥大症的头对头优效性研究。
J Clin Endocrinol Metab. 2014 Mar;99(3):791-9. doi: 10.1210/jc.2013-2480. Epub 2014 Jan 13.
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Clinical experience in the screening and management of a large kindred with familial isolated pituitary adenoma due to an aryl hydrocarbon receptor interacting protein (AIP) mutation.家族性孤立性垂体腺瘤一家系中芳香烃受体相互作用蛋白(AIP)突变的筛查和管理的临床经验。
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Pituitary tumor transforming gene and insulin-like growth factor 1 receptor expression and immunohistochemical measurement of Ki-67 as potential prognostic markers of pituitary tumors aggressiveness.
侵袭性/难治性生长激素分泌型垂体神经内分泌肿瘤的诊断与管理
Int J Endocrinol. 2024 Aug 26;2024:5085905. doi: 10.1155/2024/5085905. eCollection 2024.
4
Diagnostic, therapeutic, and prognostic characteristics of patients with acromegaly according to tumor size at diagnosis.根据诊断时肿瘤大小,肢端肥大症患者的诊断、治疗和预后特征。
Pituitary. 2024 Oct;27(5):537-544. doi: 10.1007/s11102-024-01432-w. Epub 2024 Aug 1.
5
Clinical characteristics and therapeutic outcomes of acromegalic patients with giant growth hormone-secreting pituitary adenomas: a single-center study of 67 cases.肢端肥大症患者伴巨大生长激素分泌垂体腺瘤的临床特征和治疗结局:单中心 67 例研究。
Pituitary. 2023 Dec;26(6):675-685. doi: 10.1007/s11102-023-01356-x. Epub 2023 Oct 17.
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The Prognostic-Based Approach in Growth Hormone-Secreting Pituitary Neuroendocrine Tumors (PitNET): Tertiary Reference Center, Single Senior Surgeon, and Long-Term Follow-Up.生长激素分泌型垂体神经内分泌肿瘤(PitNET)的基于预后的治疗方法:三级转诊中心、单一资深外科医生及长期随访
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Giant growth hormone-secreting pituitary adenomas from the endocrinologist's perspective.从内分泌学家的角度看生长激素分泌型垂体腺瘤。
Endocrine. 2023 Mar;79(3):545-553. doi: 10.1007/s12020-022-03241-2. Epub 2022 Nov 1.
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J Neurooncol. 2021 Jan;151(2):313-324. doi: 10.1007/s11060-020-03669-4. Epub 2021 Jan 4.
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Expert Rev Endocrinol Metab. 2020 May;15(3):171-183. doi: 10.1080/17446651.2020.1749048. Epub 2020 May 6.
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Endocrinol Nutr. 2013 Aug-Sep;60(7):358-67. doi: 10.1016/j.endonu.2012.09.005. Epub 2013 Feb 15.
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