Division of Endocrinology, School of Medicine, Catholic University, Largo A. Gemelli 8, 00168 Rome, Italy.
Pituitary. 2012 Dec;15(4):571-8. doi: 10.1007/s11102-011-0370-8.
Surgical cure cannot be achieved in most patients with invasive non-functioning pituitary macroadenoma (NFPA). Short-term residual tumor treatment with somatostatin analogs has produced disappointing results. This prospective case-control study assessed the efficacy of chronic treatment with long acting octreotide (octreotide LAR) on tumor volume in patients harboring post-surgical NFPA residue. The study population comprised 39 patients with NFPAs not cured by surgery. All patients underwent somatostatin receptor scintigraphy at least 6 months after the last surgery. Patients with a positive pituitary level octreoscan at (n = 26) received octreotide LAR (20 mg every 28 days) for ≥ 12 months (mean follow-up 37 ± 18 months) (Treated group). Moreover, a fragment of tumor tissue from patients in the treated group was retrospectively collected to assess the immunohistochemical expression of somatostatin receptor subtypes (SSTRs). The patients with a negative octreoscan (n = 13) formed the control group (mean follow-up 37 ± 16 months). Hormonal, radiological and visual field parameters were periodically assessed. In the treated group, all tumors expressed at least one SSTR subtype. The SSTR5 subtype was the most abundant, followed by SSTR3. The tumor residue increased in five of 26 patients (19%) in the treated group and in seven of 13 controls (53%). Visual field and pituitary function did not change in any patient. This study indicates that SSTR5 and SSTR3 are the most frequently expressed SSTR subtypes in NFPAs and supports a potential role of SSTR subtypes in stabilization of tumor remnant from NFPAs.
大多数侵袭性无功能垂体大腺瘤(NFPA)患者无法通过手术治愈。短期使用生长抑素类似物治疗残留肿瘤的效果并不理想。本前瞻性病例对照研究评估了长效奥曲肽(octreotide LAR)对术后 NFPA 残留患者肿瘤体积的长期治疗效果。该研究纳入了 39 例手术未能治愈的 NFPA 患者。所有患者均在最后一次手术后至少 6 个月进行了生长抑素受体闪烁显像检查。奥曲肽扫描阳性的患者(n = 26)接受 octreotide LAR(20 mg,每 28 天一次)治疗≥12 个月(平均随访 37 ± 18 个月)(治疗组)。此外,回顾性收集了治疗组患者的肿瘤组织片段,以评估生长抑素受体亚型(SSTRs)的免疫组织化学表达。奥曲肽扫描阴性的患者(n = 13)形成对照组(平均随访 37 ± 16 个月)。定期评估激素、影像学和视野参数。在治疗组中,所有肿瘤均至少表达一种 SSTR 亚型。SSTR5 亚型最为丰富,其次是 SSTR3。在治疗组的 26 例患者中有 5 例(19%)和对照组的 13 例患者中有 7 例(53%)肿瘤残留增大。任何患者的视野和垂体功能均未发生变化。本研究表明,SSTR5 和 SSTR3 是 NFPA 中最常表达的 SSTR 亚型,支持 SSTR 亚型在稳定 NFPA 肿瘤残留方面的潜在作用。