Radiotherapy and Mortality in Pituitary Adenomas

IF 4.7 3区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Baldomero González-Virla , Guadalupe Vargas-Ortega , Carlos Alfonso Romero-Gameros
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引用次数: 0

Abstract

Background

Pituitary adenomas (PA), comprising 10–20% of intracranial tumors, are classified as functioning and non-functioning and are further divided by size. Non-functioning tumors cause mechanical symptoms while functioning ones result in hormonal hypersecretion syndromes. Initial treatment involves surgery, with medical treatment for prolactinomas. Radiotherapy (RT) is employed as an adjuvant treatment, with various modalities including conventional, stereotactic radiosurgery (SRS), and fractionated stereotactic RT (FSRT). Although effective, RT is associated with complications and toxicities such as hypopituitarism, optic neuritis, secondary CNS tumors, and neurocognitive deficits.

Aim

Describe the information on mortality from radiotherapy as treatment of functioning PA.

Methods

A PubMed search spanning 2000–2017 was conducted for articles on pituitary RT.

Results

Conventional RT entails high-energy radiation over multiple sessions, while SRS delivers precise high doses in a single session. FSRT offers enhanced precision using a linear accelerator, delivering multiple doses. Optic structure proximity and tumor volume dictate RT modality. Studies have shown SRS and FSRT's efficacy in tumor and endocrine control, with variable risks and complications. Mortality rates in pituitary adenomas treated with RT have been evaluated, revealing complexities. Acromegaly, associated with increased mortality due to cerebrovascular disease, may result from RT. Irradiation of non-functioning pituitary macroadenomas also elevates cerebrovascular risk, while radiotherapy-induced hypopituitarism is associated with increased cardiovascular mortality. RT-induced damage is attributed to microvascular lesions and arteriolar changes.

Conclusion

Modern techniques mitigate complications, and although safer, long-term studies are needed. Multidisciplinary evaluation guides the treatment decision, optimizing efficacy and minimizing risk, ultimately improving the patient's quality of life.

垂体腺瘤的放射治疗与死亡率。
背景:垂体腺瘤(PA)占颅内肿瘤的10-20%,分为功能性和非功能性,并按大小进一步划分。非功能性肿瘤会引起机械症状,而功能性肿瘤则会导致激素分泌过多综合征。最初的治疗包括手术和泌乳素瘤的药物治疗。放射治疗(RT)是一种辅助治疗方法,包括常规、立体定向放射外科(SRS)和分级立体定向放射治疗(FSRT)。尽管有效,RT与并发症和毒性有关,如垂体功能减退、视神经炎、继发性中枢神经系统肿瘤和神经认知缺陷。目的:描述放射治疗功能性PA的死亡率信息。方法:PubMed在2000-2017年间对垂体RT的文章进行了检索。结果:常规RT需要多次高能辐射,而SRS在单次治疗中提供精确的高剂量。FSRT使用线性加速器提供了更高的精度,可提供多种剂量。光学结构接近度和肿瘤体积决定了RT模式。研究表明,SRS和FSRT在肿瘤和内分泌控制方面具有疗效,风险和并发症各不相同。对RT治疗垂体腺瘤的死亡率进行了评估,揭示了复杂性。肢端肥大症与脑血管疾病导致的死亡率增加有关,可能由RT引起。对功能不全的垂体大腺瘤进行放疗也会增加脑血管风险,而放疗诱导的垂体功能减退与心血管死亡率增加有关。RT诱导的损伤可归因于微血管病变和小动脉变化。结论:现代技术可以减轻并发症,尽管更安全,但还需要长期研究。多学科评估指导治疗决策,优化疗效并将风险降至最低,最终提高患者的生活质量。
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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来源期刊
Archives of Medical Research
Archives of Medical Research 医学-医学:研究与实验
CiteScore
12.50
自引率
0.00%
发文量
84
审稿时长
28 days
期刊介绍: Archives of Medical Research serves as a platform for publishing original peer-reviewed medical research, aiming to bridge gaps created by medical specialization. The journal covers three main categories - biomedical, clinical, and epidemiological contributions, along with review articles and preliminary communications. With an international scope, it presents the study of diseases from diverse perspectives, offering the medical community original investigations ranging from molecular biology to clinical epidemiology in a single publication.
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