Department of Radiation Oncology; Department of Neuro-Oncology Disease Management Group, TMH/ACTREC, Tata Memorial Centre, Homi Bhabha National Institute (HBNI), Mumbai, Maharashtra, India.
Neurol India. 2020 May-Jun;68(Supplement):S113-S122. doi: 10.4103/0028-3886.287678.
Pituitary adenomas are benign tumors arising in the adenohypophysis and comprise 8%-20% of all reported primary brain tumors in the west. Transsphenoidal surgery with an aim to achieve complete tumor resection is the recommended first-line treatment for nonfunctioning as well as secretory pituitary adenoma. External beam radiation therapy (RT) has been demonstrated to be an effective treatment modality for pituitary adenoma, uncured by surgery and/or medical therapy, providing excellent long-term local control (>90%), but lower and variable rates (50%-80%) of biochemical remission in secretory tumors. The adoption of pituitary RT in the community has been limited due to concerns regarding potential late toxicity and long latency in normalization of hormonal hypersecretion. Over the years, technological advances in RT planning and delivery have resulted in progressive conformation of high doses to the target tissues while sparing adjacent neurovascular structures providing a favorable therapeutic index. The choice of RT technique should be based on size, site, and availability of infrastructure and expertise, with no significant differences between fractionated approaches and stereotactic radiosurgery (SRS). In contemporary clinical practice, the recommended dose of fractionated RT for pituitary adenoma is 45-50.4Gy in 25-28 fractions delivered over 5-6 weeks using modern high-precision techniques. The recommended dose of SRS given in a single fraction is 12-14Gy for nonfunctioning adenomas and 16-20Gy for secretory tumors. Late toxicity of pituitary RT includes hypopituitarism, neurocognitive impairment, neuropsychological dysfunction, optic neuropathy, cerebrovascular accidents, and second malignant neoplasms. Hence, RT in pituitary adenoma should be offered only to patients with residual, recurrent, progressive, or high-risk tumors with careful assessment of the benefit-risk ratio by an experienced multidisciplinary neurooncology team.
垂体腺瘤是起源于腺垂体的良性肿瘤,占西方报道的所有原发性脑肿瘤的 8%-20%。经蝶窦手术旨在实现肿瘤完全切除,是无功能和分泌性垂体腺瘤的推荐一线治疗方法。外照射放疗(RT)已被证明是一种有效的治疗方法,对于手术和/或药物治疗未治愈的垂体腺瘤,提供了极好的长期局部控制(>90%),但分泌性肿瘤的生化缓解率较低且变化较大(50%-80%)。由于担心潜在的晚期毒性和激素分泌过度正常化的潜伏期较长,社区中采用垂体 RT 受到限制。多年来,RT 计划和交付方面的技术进步导致目标组织的高剂量逐渐形成,同时保护相邻的神经血管结构,提供了有利的治疗指数。RT 技术的选择应基于肿瘤的大小、位置以及基础设施和专业知识的可用性,分阶段方法和立体定向放射外科(SRS)之间没有显著差异。在当代临床实践中,推荐的垂体腺瘤分割 RT 剂量为 45-50.4Gy,在 5-6 周内使用现代高精度技术分 25-28 次给予。单次分割 SRS 推荐剂量为 12-14Gy 用于无功能腺瘤,16-20Gy 用于分泌性肿瘤。垂体 RT 的晚期毒性包括垂体功能减退、神经认知障碍、神经心理学功能障碍、视神经病变、脑血管意外和第二恶性肿瘤。因此,只有在对有残留、复发、进展或高危肿瘤的患者进行仔细的获益风险评估后,由经验丰富的多学科神经肿瘤学团队提供垂体腺瘤的 RT。