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侵袭性垂体腺瘤的分子诊断与药物治疗策略进展

Advancements in Molecular Diagnosis and Pharmacotherapeutic Strategies for Invasive Pituitary Adenomas.

作者信息

Xu Dingkai, Wang Ling, Zheng Maohua

机构信息

Department of Neurosurgery, The First Hospital of Lanzhou University, Lanzhou, China.

Department of Endocrinology, Liangzhou Hospital, Wuwei, Gansu, China.

出版信息

Immun Inflamm Dis. 2024 Dec;12(12):e70098. doi: 10.1002/iid3.70098.

Abstract

BACKGROUND

The overwhelming majority of pituitary tumors consist of pituitary adenomas (PAs), which have recently also been termed pituitary neuroendocrine tumors (PitNETs). Clinically significant PAs occur in approximately one in every 1000 individuals, while other types of pituitary tumors, such as craniopharyngiomas and pituicytomas, are significantly less common. Although PAs are generally benign, a subset of them exhibits malignant-like biological traits. They tend to infiltrate and grow aggressively into adjacent tissues and organs, including the dura mater, cavernous sinus, and sphenoid sinus. This invasive behavior often results in the destruction of the normal anatomical architecture of the sella turcica and skull base. Clinically, such tumors are classified as invasive PAs (IPAs), emphasizing their aggressive and destructive nature.

OBJECTIVE AND SIGNIFICANCE

Currently, the diagnostic indicators for IPAs frequently suffer from suboptimal sensitivity and specificity. The invasiveness assessment of PAs lacks a definitive gold standard and instead serves as a predictive tool, with a greater number of indicators met suggesting a higher likelihood of invasiveness. Consequently, a comprehensive approach that integrates imaging, pathological, molecular biological, and other disciplinary metrics is crucial for accurate evaluation. Despite surgery being the primary treatment modality for IPAs, their malignant-like behavior complicates complete resection, resulting in lower resection rates and heightened postoperative recurrence, necessitating multiple surgeries. Therefore, adjunctive drug therapy is often necessary for IPA patients. Preoperative drug therapy can shrink tumor size, facilitating resection and postoperative recovery, mitigating hormone imbalances, delaying recurrence, and enhancing patients' quality of life.

CONCLUSIONS

This article comprehensively reviews the diagnostic criteria for assessing the invasiveness of PAs in the domains of imaging, pathology, and molecular biology, provides an overview of the current research status of drug therapy for these conditions, and deepens our insight into the biological and therapeutic aspects of the tumor microenvironment in PAs.

摘要

背景

绝大多数垂体肿瘤由垂体腺瘤(PAs)组成,垂体腺瘤最近也被称为垂体神经内分泌肿瘤(PitNETs)。具有临床意义的垂体腺瘤在每1000人中约有1例发生,而其他类型的垂体肿瘤,如颅咽管瘤和垂体细胞瘤,则明显较少见。虽然垂体腺瘤通常是良性的,但其中一部分表现出类似恶性的生物学特征。它们倾向于浸润并向邻近组织和器官,包括硬脑膜、海绵窦和蝶窦,进行侵袭性生长。这种侵袭行为常常导致蝶鞍和颅底正常解剖结构的破坏。临床上,这类肿瘤被归类为侵袭性垂体腺瘤(IPAs),强调其侵袭性和破坏性本质。

目的和意义

目前,侵袭性垂体腺瘤的诊断指标常常存在敏感性和特异性欠佳的问题。垂体腺瘤的侵袭性评估缺乏明确的金标准,而是作为一种预测工具,满足的指标数量越多,侵袭的可能性就越高。因此,整合影像学、病理学、分子生物学和其他学科指标的综合方法对于准确评估至关重要。尽管手术是侵袭性垂体腺瘤的主要治疗方式,但其类似恶性的行为使完整切除变得复杂,导致切除率降低和术后复发率升高,需要多次手术。因此,侵袭性垂体腺瘤患者通常需要辅助药物治疗。术前药物治疗可以缩小肿瘤大小,便于切除和术后恢复,减轻激素失衡,延缓复发,并提高患者的生活质量。

结论

本文全面综述了在影像学、病理学和分子生物学领域评估垂体腺瘤侵袭性的诊断标准,概述了这些疾病药物治疗的当前研究现状,并加深了我们对垂体腺瘤肿瘤微环境的生物学和治疗方面的认识。

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