Recent advances in understanding and managing pituitary adenomas.

Faculty reviews Pub Date : 2023-01-01 DOI:10.12703/r/12-6
Maria Markou, Aikaterini Lavrentaki, Georgia Ntali
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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.

垂体腺瘤的认识和治疗的最新进展。
垂体腺瘤是一种常见的颅内肿瘤。尽管它们是良性的,但PAs可能会引起严重的疾病负担,导致激素紊乱或局部压迫。一部分PAs表现出难以预测的侵袭性行为,在极少数情况下它们会转移。因此,早期诊断和治疗非常重要。分子病理学的进步提高了对其发病机制的理解,并提供了识别和靶向新途径的机会。改进的成像和功能分子技术可以精确检测甚至非常小的肿瘤并指导靶向治疗。经蝶窦手术是大多数PAs的一线治疗方法,内窥镜神经外科领域的进展提供了良好的结果。传统上,多巴胺激动剂(DAs)是治疗催乳素瘤的一线药物。对于肢端肥大症患者,当手术不成功或无指征时,应用第一代和第二代生长抑素类似物(SSAs)。对于库欣病(CD),针对肾上腺甾体生成、垂体生长抑素受体和糖皮质激素受体的药物用于治疗持续性或复发性CD患者的高皮质醇症,对于那些不适合手术的患者,以及作为接受放射治疗直到皮质醇水平得到控制的患者的桥梁治疗。替莫唑胺(TMZ)是侵袭性PAs的一线化疗药物,但现在有新的实验疗法,如抗血管内皮生长因子(anti-VEGF)治疗、雷帕霉素(mTOR)抑制剂的机制靶点、酪氨酸激酶抑制剂、细胞周期和检查点抑制剂。放射治疗提供给肿瘤残留、复发或进展的患者。放射治疗计划和递送的现代技术能够在保留重要结构的同时向目标组织提供高剂量。随着我们对PAs的生物学行为的熟悉和我们的治疗手段的扩大,我们的下一个目标是为每个患者量身定制和个性化治疗,以达到最佳效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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