[Aggressive pituitary tumors and carcinomas: modern classification, advances and prospects in treatment].

Q4 Medicine
L I Astafyeva, P L Kalinin, G L Kobyakov, Yu Yu Trunin, M V Ryzhova
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引用次数: 0

Abstract

Despite slow growth of most pituitary tumors and high rates of total resection and/or effective therapy, pituitary neoplasms are characterized by aggressive behavior with high growth rate, frequent relapses and resistance to standard treatments in 10% of cases. In modern WHO classifications of tumors of the central nervous system, endocrine and neuroendocrine tumors, the authors propose the definition «pituitary neuroendocrine tumor» instead of previous «pituitary adenoma» and «metastasizing pituitary neuroendocrine tumor» instead of «pituitary carcinoma». Currently, there are no effective prognostic markers of aggressive tumors. This complicates early diagnosis. It is proposed to apply a five-stage prognostic classification based on proliferation rate (including mitotic count, Ki-67 index and p53 immunoexpression) and morphometric markers of invasiveness for all resected pituitary neoplasms. This approach would be valuable for earlier detection of aggressive tumors and pituitary carcinomas. Compression of visual pathways, third ventricle and brain stem due to rapid growth of aggressive tumors usually requires redo surgeries with subsequent radiotherapy. Hormonally active tumors require therapy with somatostatin analogues and dopamine agonists in maximum possible doses. Chemotherapy with temozolomide as first-line option is recommended if standard treatment is ineffective. Alternative treatment includes peptide receptor radionuclide therapy (PRRT), molecular targeted therapy (bevacizumab, tyrosine kinase inhibitors, everolimus and cyclin-dependent kinase inhibitors) and immunotherapy (checkpoint inhibitors). Considering the need for combined treatment, these cases should always be discussed by a multidisciplinary team (neurosurgeon, endocrinologist, radiotherapist, oncologist, pathologist) with necessary qualifications and experience in treating these patients. Treatment of aggressive tumors and pituitary carcinomas is becoming an active and rapidly developing direction in neurosurgery, endocrinology and oncology.

[侵袭性垂体瘤和癌:现代分类、治疗进展和前景]。
尽管大多数垂体瘤生长缓慢,全切除率和/或有效治疗率较高,但垂体瘤的特点是侵袭性强、生长率高、复发频繁,10%的病例对标准治疗有抵抗力。在世界卫生组织对中枢神经系统肿瘤、内分泌肿瘤和神经内分泌肿瘤的现代分类中,作者提出了 "垂体神经内分泌肿瘤 "的定义,而不是以前的 "垂体腺瘤",也提出了 "转移性垂体神经内分泌肿瘤 "的定义,而不是 "垂体癌"。目前,侵袭性肿瘤还没有有效的预后标志物。这使得早期诊断变得复杂。建议对所有切除的垂体肿瘤采用基于增殖率(包括有丝分裂计数、Ki-67 指数和 p53 免疫表达)和侵袭性形态计量标记的五阶段预后分类。这种方法对早期发现侵袭性肿瘤和垂体癌很有价值。侵袭性肿瘤快速生长导致视觉通路、第三脑室和脑干受压,通常需要重新进行手术,并随后进行放射治疗。激素活跃的肿瘤需要使用最大剂量的体生长抑素类似物和多巴胺激动剂进行治疗。如果标准治疗无效,建议将替莫唑胺化疗作为一线选择。替代治疗包括肽受体放射性核素治疗(PRRT)、分子靶向治疗(贝伐珠单抗、酪氨酸激酶抑制剂、依维莫司和细胞周期蛋白依赖性激酶抑制剂)和免疫治疗(检查点抑制剂)。考虑到联合治疗的必要性,这些病例应始终由具有治疗此类患者的必要资质和经验的多学科团队(神经外科医生、内分泌科医生、放射治疗医生、肿瘤科医生、病理科医生)进行讨论。侵袭性肿瘤和垂体癌的治疗正成为神经外科、内分泌学和肿瘤学中一个活跃而快速发展的方向。
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
CiteScore
0.70
自引率
0.00%
发文量
75
期刊介绍: Scientific and practical peer-reviewed journal. This publication covers the theoretical, practical and organizational problems of modern neurosurgery, the latest advances in the treatment of various diseases of the central and peripheral nervous system. Founded in 1937. English version of the journal translates from Russian version since #1/2013.
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