Astafieva L I, Chernov I V, Kobyakov G L, Trunin Yu Yu, Shishkina L V, Shkarubo A N, Fomichev D V, Sidneva Yu G, Vagapova G R, Kalinin P L
Burdenko Neurosurgical Center, Moscow, Russia.
Botkin Moscow Multidisciplinary Scientific Clinical Center, Moscow, Russia.
Zh Vopr Neirokhir Im N N Burdenko. 2025;89(1):83-93. doi: 10.17116/neiro20258901183.
According to the modern WHO classification, pituitary carcinomas (or metastatic neuroendocrine pituitary tumors) are pituitary tumors with confirmed craniospinal and/or distant metastases. The main goal of histological analysis of pituitary carcinomas is to confirm pituitary origin of metastases. Treatment usually includes surgery and radiotherapy, dopamine agonists in maximum possible doses in case of prolactin-secreting pituitary carcinomas and chemotherapy with preferable temozolomide.
To present the results of diagnosis and treatment of two patients with prolactin-secreting pituitary carcinomas.
The authors describe 2 patients with prolactin-secreting pituitary carcinomas arising from drug-resistant aggressive prolactinomas with histologically confirmed metastases. In both cases, combined treatment included surgery, radio- and chemotherapy (cabergoline and temozolomide).
A 47-year-old patient underwent surgery, radio- and dopamine agonist therapy with subsequent regression of tumor growth in the follow-up period. However, progressive increase in prolactin concentration necessitated PET/CT with detection of multiple metastases in bones and lymph nodes. Temozolomide therapy led to temporary shrinkage of metastatic foci with subsequent progression. The second case was characterized by multiple brain and spinal cord metastases in a 47-year-old woman. Resection of intracranial metastasis and temozolomide therapy stabilized the disease and normalized serum prolactin throughout 2-year follow-up with subsequent progression.
Pituitary carcinoma is a rare tumor with unfavorable prognosis. Treatment is currently not standardized and determined by available world experience regarding various chemotherapeutic drugs. Temozolomide is the most effective drug. However, short-term remission is usually followed by subsequent disease progression in most cases.
根据现代世界卫生组织的分类,垂体癌(或转移性神经内分泌垂体肿瘤)是已证实有颅脊髓和/或远处转移的垂体肿瘤。垂体癌组织学分析的主要目的是确认转移灶的垂体起源。治疗通常包括手术和放疗,对于分泌催乳素的垂体癌,尽可能使用最大剂量的多巴胺激动剂,以及首选替莫唑胺的化疗。
介绍两例分泌催乳素的垂体癌患者的诊断和治疗结果。
作者描述了2例由耐药性侵袭性催乳素瘤引起且组织学证实有转移的分泌催乳素的垂体癌患者。两例患者均采用了手术、放疗和化疗(卡麦角林和替莫唑胺)的联合治疗。
一名47岁患者接受了手术、放疗和多巴胺激动剂治疗,随后在随访期间肿瘤生长出现消退。然而,催乳素浓度的逐渐升高使得进行PET/CT检查,结果发现骨骼和淋巴结有多处转移。替莫唑胺治疗导致转移灶暂时缩小,但随后病情进展。第二例是一名47岁女性,有多处脑和脊髓转移。颅内转移灶切除及替莫唑胺治疗使病情稳定,在2年的随访期间血清催乳素恢复正常,但随后病情仍进展。
垂体癌是一种罕见的肿瘤,预后不佳。目前治疗尚未标准化,而是由关于各种化疗药物的现有世界经验决定。替莫唑胺是最有效的药物。然而,在大多数情况下,短期缓解后通常会出现疾病进展。