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垂体腺瘤的认识与管理的最新进展

Recent advances in understanding and managing pituitary adenomas.

作者信息

Markou Maria, Lavrentaki Aikaterini, Ntali Georgia

机构信息

Private Endocrinology, Diabetes and Metabolism Clinic, Daidalou 11, Levadia, 32131, Greece.

Department of Endocrinology, Diabetes and Metabolism, Evangelismos Hospital, 10676 Athens, Greece.

出版信息

Fac Rev. 2023 Mar 21;12:6. doi: 10.12703/r/12-6. eCollection 2023.

Abstract

Pituitary adenomas (PAs) are common intracranial tumors. Despite their benign nature, PAs may cause a significant burden of disease, leading to either hormonal disturbances or local compression. A subset of PAs presents an aggressive behavior that remains difficult to predict, and in rare cases they metastasize. Therefore, early diagnosis and treatment are important. Advances in molecular pathology have improved the understanding of their pathogenesis and offer opportunities to identify and target novel pathways. Improved imaging and functional molecular techniques precisely detect even very small tumors and guide targeted treatment. Transsphenoidal surgery is the first-line treatment for the majority of PAs, and advances in the field of endoscopic neurosurgery offer excellent outcomes. Dopamine agonists (DAs) are traditionally the first-line treatment for prolactinomas. For patients with acromegaly, first- and second-generation somatostatin analogues (SSAs) are applied when surgery is not successful or not indicated. For Cushing's disease (CD), drugs targeting adrenal steroidogenesis, somatostatin receptors in the pituitary, and glucocorticoid receptors are used to treat hypercortisolism in patients with persistent or recurrent CD, for those who are not good surgical candidates, and as a bridge treatment for those who have undergone radiation treatment until cortisol levels are controlled. Temozolomide (TMZ) is the first-line chemotherapy for aggressive PAs, but new experimental therapies, like the anti-vascular endothelial growth factor (anti-VEGF) therapy, mechanistic target of rapamycin (mTOR) inhibitors, tyrosine kinase inhibitors, and cell cycle and checkpoint inhibitors, are now available. Radiotherapy is offered to patients with residual, recurrent, or progressive tumors. Modern techniques in radiotherapy planning and delivery are able to deliver high doses to the target tissue while sparing vital structures. As we familiarize ourselves with the biological behavior of PAs and our therapeutic armamentarium expands, the next goal is to tailor and personalize treatment to each individual patient so as to achieve the best outcome.

摘要

垂体腺瘤(PAs)是常见的颅内肿瘤。尽管其本质为良性,但垂体腺瘤可能导致重大疾病负担,引发激素紊乱或局部压迫。一部分垂体腺瘤表现出侵袭性行为,难以预测,且在罕见情况下会发生转移。因此,早期诊断和治疗至关重要。分子病理学的进展加深了对其发病机制的理解,并为识别和靶向新途径提供了机会。改进的成像和功能分子技术能够精确检测出极小的肿瘤并指导靶向治疗。经蝶窦手术是大多数垂体腺瘤的一线治疗方法,内镜神经外科领域的进展带来了出色的治疗效果。多巴胺激动剂(DAs)传统上是催乳素瘤的一线治疗药物。对于肢端肥大症患者,当手术不成功或不适用时,会应用第一代和第二代生长抑素类似物(SSAs)。对于库欣病(CD),针对肾上腺类固醇生成、垂体中的生长抑素受体以及糖皮质激素受体的药物,用于治疗持续性或复发性CD患者、不适合手术的患者以及作为接受放射治疗患者的过渡治疗,直至皮质醇水平得到控制。替莫唑胺(TMZ)是侵袭性垂体腺瘤的一线化疗药物,但现在有了新的实验性疗法,如抗血管内皮生长因子(抗VEGF)疗法、雷帕霉素靶蛋白(mTOR)抑制剂酪氨酸激酶抑制剂以及细胞周期和检查点抑制剂。对于有残留、复发或进展性肿瘤的患者会提供放射治疗。放射治疗计划和实施中的现代技术能够在保护重要结构的同时,向靶组织输送高剂量辐射。随着我们熟悉垂体腺瘤的生物学行为且治疗手段不断扩展,下一个目标是为每位患者量身定制个性化治疗方案,以实现最佳治疗效果。

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Overview of the 2022 WHO Classification of Pituitary Tumors.《2022 年世卫组织垂体肿瘤分类概述》。
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