Raverot Gerald, Burman Pia, McCormack Ann, Heaney Anthony, Petersenn Stephan, Popovic Vera, Trouillas Jacqueline, Dekkers Olaf M
Fédération d'Endocrinologie, Centre de Référence des Maladies Rares Hypophysaires HYPO, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France.
Faculté de Médecine Lyon Est, Université Lyon 1, Lyon, France.
Eur J Endocrinol. 2018 Jan;178(1):G1-G24. doi: 10.1530/EJE-17-0796. Epub 2017 Oct 18.
Pituitary tumours are common and easily treated by surgery or medical treatment in most cases. However, a small subset of pituitary tumours does not respond to standard medical treatment and presents with multiple local recurrences (aggressive pituitary tumours) and in rare occasion with metastases (pituitary carcinoma). The present European Society of Endocrinology (ESE) guideline aims to provide clinical guidance on diagnosis, treatment and follow-up in aggressive pituitary tumours and carcinomas.
We decided upfront, while acknowledging that literature on aggressive pituitary tumours and carcinomas is scarce, to systematically review the literature according to the GRADE (Grading of Recommendations Assessment, Development and Evaluation) system. The review focused primarily on first- and second-line treatment in aggressive pituitary tumours and carcinomas. We included 14 single-arm cohort studies (total number of patients = 116) most on temozolomide treatment ( = 11 studies, total number of patients = 106). A positive treatment effect was seen in 47% (95% CI: 36-58%) of temozolomide treated. Data from the recently performed ESE survey on aggressive pituitary tumours and carcinomas (165 patients) were also used as backbone for the guideline. SELECTED RECOMMENDATION: (i) Patients with aggressive pituitary tumours should be managed by a multidisciplinary expert team. (ii) Histopathological analyses including pituitary hormones and proliferative markers are needed for correct tumour classification. (iii) Temozolomide monotherapy is the first-line chemotherapy for aggressive pituitary tumours and pituitary carcinomas after failure of standard therapies; treatment evaluation after 3 cycles allows identification of responder and non-responder patients. (iv) In patients responding to first-line temozolomide, we suggest continuing treatment for at least 6 months in total. Furthermore, the guideline offers recommendations for patients who recurred after temozolomide treatment, for those who did not respond to temozolomide and for patients with systemic metastasis.
垂体瘤很常见,大多数情况下通过手术或药物治疗很容易治愈。然而,一小部分垂体瘤对标准药物治疗无反应,会出现多次局部复发(侵袭性垂体瘤),极少数情况下会发生转移(垂体癌)。欧洲内分泌学会(ESE)现行指南旨在为侵袭性垂体瘤和垂体癌的诊断、治疗及随访提供临床指导。
我们预先决定,尽管认识到关于侵袭性垂体瘤和垂体癌的文献稀缺,但仍根据推荐分级评估、制定与评价(GRADE)系统对文献进行系统回顾。该综述主要聚焦于侵袭性垂体瘤和垂体癌的一线及二线治疗。我们纳入了14项单臂队列研究(患者总数 = 116),其中大多数研究( = 11项研究,患者总数 = 106)是关于替莫唑胺治疗的。接受替莫唑胺治疗的患者中有47%(95%置信区间:36 - 58%)显示出积极的治疗效果。最近进行的ESE关于侵袭性垂体瘤和垂体癌的调查(165例患者)的数据也被用作该指南的基础。选定的建议:(i)侵袭性垂体瘤患者应由多学科专家团队管理。(ii)为进行正确的肿瘤分类,需要进行包括垂体激素和增殖标志物在内的组织病理学分析。(iii)替莫唑胺单药治疗是标准治疗失败后侵袭性垂体瘤和垂体癌的一线化疗方法;3个周期后的治疗评估可识别有反应和无反应的患者。(iv)对于对一线替莫唑胺有反应的患者,我们建议总共持续治疗至少6个月。此外,该指南还为替莫唑胺治疗后复发的患者、对替莫唑胺无反应的患者以及有全身转移的患者提供了建议。