Tóth Miklós
1 Semmelweis Egyetem, Belgyógyászati és Onkológiai Klinika, Endo-ERN Központ Budapest, Korányi S. u. 2/A, 1083 Magyarország.
Orv Hetil. 2023 Jul 30;164(30):1167-1175. doi: 10.1556/650.2023.32832.
Anterior pituitary tumours, once considered benign neoplasms, may rarely have aggressive behaviour and can even metastasize. The current guideline of the European Society of Endocrinology defines aggressive pituitary adenomas as radiologically invasive tumours with an unusually rapid growth rate and frequent relapses despite the optimal use of standard therapies. Currently, there is not any single, well-defined pathological marker of malignancy. Pituitary carcinomas are thus clinically defined by the presence of craniospinal or distant metastases, typically developing several years after the first presentation. Histopathology may predict aggressive behaviour if the Ki67 index and mitotic rate are elevated and in case of positive p53 staining. These patients' short- and long-term therapy should be individualized and regularly discussed by a multidisciplinary pituitary team. Besides standard medical treatment administered in maximally tolerated doses, current recommendations suggest repeated surgery and radiotherapy. If this approach fails, the next choice of treatment is chemotherapy with temozolomide. After that, immune checkpoint inhibitors, bevacizumab, and peptide receptor radiotherapy are emerging therapies that should be used on a case-by-case basis. Orv Hetil. 2023; 164(30): 1167-1175.
垂体前叶肿瘤曾被认为是良性肿瘤,但极少数情况下可能具有侵袭性,甚至会发生转移。欧洲内分泌学会的现行指南将侵袭性垂体腺瘤定义为具有放射学侵袭性、生长速度异常快且尽管最佳使用标准疗法仍频繁复发的肿瘤。目前,尚无任何单一的、明确的恶性病理标志物。因此,垂体癌在临床上是通过存在颅脊髓或远处转移来定义的,通常在首次出现症状数年后发生。如果Ki67指数和有丝分裂率升高以及p53染色呈阳性,组织病理学可能预示侵袭性行为。这些患者的短期和长期治疗应个体化,并由多学科垂体团队定期讨论。除了以最大耐受剂量进行标准药物治疗外,目前的建议还包括重复手术和放疗。如果这种方法失败,接下来的治疗选择是使用替莫唑胺进行化疗。在此之后,免疫检查点抑制剂、贝伐单抗和肽受体放疗是正在出现的治疗方法,应根据具体情况使用。《匈牙利医学周报》。2023年;164(30):1167 - 1175。