Department of Radiation Oncology, Mayo Clinic, Jacksonville, Florida.
Department of Neurological Surgery, University of Virginia, Charlottesville, Virginia.
Int J Radiat Oncol Biol Phys. 2018 Jul 1;101(3):610-617. doi: 10.1016/j.ijrobp.2018.02.023. Epub 2018 Feb 20.
To compare and describe the time to endocrine remission and new hypopituitarism among patients with growth hormone (GH) and adrenocorticotropic hormone (ACTH)-secreting pituitary adenomas after radiosurgery, controlling for several known prognostic factors.
An institutional review board-approved, institutional retrospective analysis of patients with GH- and ACTH-secreting pituitary adenomas was performed, with matching for patient sex, age at radiosurgery, interval between the last resection and radiosurgery, use of previous radiation therapy, whole sella treatment, suprasellar extension, cavernous sinus invasion, and margin dose. Endocrine remission was defined as a normal serum insulin-like growth factor-1 (GH secreting) or a normal 24-hour urine-free cortisol (ACTH secreting) level without suppressive medications. Endocrine remission and the incidence of new hypopituitarism after single-fraction radiosurgery were recorded and compared between the 2 groups.
The data from 242 patients were evaluated, 121 with GH-secreting tumors and 121 with ACTH-secreting tumors. Of the 242 patients, 75% had cavernous sinus invasion and 10% had suprasellar extension at radiosurgery. The median radiosurgical marginal dose was 25 Gy to the 50% isodose line between each group. After multivariable adjustment, the factors associated with an increased time to endocrine remission included patient age (hazard ratio [HR] 1.016; P = .023), cavernous sinus invasion (HR 1.793; P = .004), and the presence of acromegaly (HR 2.912; P < .001). The incidence of new hypopituitarism developing after stereotactic radiosurgery was 29% and did not appreciably differ by adenoma subtype (P = .180).
After radiosurgery, patients with ACTH-secreting tumors achieved endocrine remission sooner than did those with GH-secreting tumors. These results provide insight into the relative tumor biology and disease course after radiosurgery that will serve to further improve clinical outcomes and patient treatment in the future.
通过控制多个已知预后因素,比较并描述经放射外科治疗后分泌生长激素(GH)和促肾上腺皮质激素(ACTH)的垂体腺瘤患者达到内分泌缓解的时间和新发垂体功能减退症的时间。
对经放射外科治疗的分泌 GH 和 ACTH 的垂体腺瘤患者进行了机构审查委员会批准的机构回顾性分析,并对患者性别、放射外科时的年龄、上次切除与放射外科之间的时间间隔、以前是否使用过放射治疗、全鞍治疗、鞍上扩展、海绵窦侵袭以及边缘剂量进行了匹配。内分泌缓解定义为血清胰岛素样生长因子-1(GH 分泌)正常或 24 小时尿游离皮质醇(ACTH 分泌)正常而无需抑制性药物。记录并比较两组患者接受单次分割放射外科治疗后的内分泌缓解率和新发垂体功能减退症的发生率。
共评估了 242 例患者的数据,其中 121 例为 GH 分泌性肿瘤,121 例为 ACTH 分泌性肿瘤。在 242 例患者中,75%有海绵窦侵袭,10%有鞍上扩展。两组的放射外科边缘剂量中位数为 25Gy,在每条等剂量线 50%处。多变量调整后,与内分泌缓解时间延长相关的因素包括患者年龄(危险比[HR]1.016;P=0.023)、海绵窦侵袭(HR 1.793;P=0.004)和存在肢端肥大症(HR 2.912;P<0.001)。立体定向放射外科治疗后新发垂体功能减退症的发生率为 29%,与腺瘤亚型无显著差异(P=0.180)。
经放射外科治疗后,ACTH 分泌性肿瘤患者达到内分泌缓解的时间早于 GH 分泌性肿瘤患者。这些结果提供了关于放射外科治疗后相对肿瘤生物学和疾病过程的见解,这将有助于未来进一步改善临床结果和患者治疗。