| Literature DB >> 26961771 |
Hiromitsu Iwata1,2, Kengo Sato3, Ryutaro Nomura3, Yusuke Tabei3, Ichiro Suzuki3, Naoki Yokota4,5, Mitsuhiro Inoue6, Seiji Ohta4, Shozo Yamada7, Yuta Shibamoto8.
Abstract
The aim of the present study was to evaluate the safety and feasibility of hypofractionated stereotactic radiotherapy (SRT) with CyberKnife for growth hormone-secreting pituitary adenoma (GH-PA). Fifty-two patients with GH-PA were treated with hypofractionated SRT between September 2001 and October 2012. Eight patients had clinically silent GH-PA and 44 were symptomatic. Only 1 patient was inoperable. The other patients had recurrent or postoperative residual tumors on MRI. All patients had received pharmacotherapy prior to SRT with a somatostatin analog, dopamine agonist, and/or GH receptor antagonist. The marginal doses were 17.4-26.8 Gy for the 3-fraction schedule and 20.0-32.0 Gy for the 5-fraction schedule. Endocrinological remission was assessed by the Cortina consensus criteria 2010 (random GH <1 ng/ml or nadir GH after an oral glucose tolerance test <0.4 ng/ml and normalization of age- and sex-adjusted insulin-like growth factor-1). The median follow-up period was 60 months (range 27-137). The 5-year overall survival, local control, and disease-free survival rates were 100, 100, and 96 %, respectively. Nine patients (5 clinically silent and 4 symptomatic patients) satisfied the Cortina criteria without receiving further pharmacotherapy, whereas the remaining 43 patients did not. No post-SRT grade 2 or higher visual disorder occurred. Symptomatic post-SRT hypopituitarism was observed in 1 patient. CyberKnife hypofractionated SRT is safe and effective when judged by imaging findings for GH-PA. However, it may be difficult to satisfy the Cortina consensus criteria in most symptomatic patients with SRT alone. Further investigations of optimal treatments are warranted.Entities:
Keywords: Cortina consensus; CyberKnife; Growth hormone-secreting pituitary adenoma; Hypofractionated stereotactic radiotherapy; Optic pathway
Mesh:
Year: 2016 PMID: 26961771 DOI: 10.1007/s11060-016-2105-1
Source DB: PubMed Journal: J Neurooncol ISSN: 0167-594X Impact factor: 4.130