Barkan A L, Lloyd R V, Chandler W F, Hatfield M K, Gebarski S S, Kelch R P, Beitins I Z
Department of Internal Medicine (Endocrinology), University Hospital, University of Michigan Medical Center, Ann Arbor 48105.
J Clin Endocrinol Metab. 1988 Nov;67(5):1040-8. doi: 10.1210/jcem-67-5-1040.
Ten patients with previously untreated acromegaly and invasive pituitary macroadenomas were treated with the long-acting somatostatin analog SMS 201-995 (Sandoz) for 3-30 weeks before transsphenoidal or subfrontal pituitary adenomectomy. Preoperatively, treatment with SMS 201-995 reduced mean 24-h plasma GH concentrations from 8.5-66.7 to below 4.6 micrograms/L in eight patients and by 60-80% in the remaining two patients. Pituitary tumor size decreased 20-54%. Morphologically, the tumors showed decreased total cell, cytoplasmic, and nuclear areas; varying degrees of perivascular fibrosis; and dense granularity. Postoperatively, plasma GH and insulin-like growth factor I concentrations fell into the normal range, and GH dynamics became normal in eight patients. In the remaining two patients mild GH hypersecretion persisted after surgery (mean fasting and random plasma GH, 6.1 and 7.9 micrograms/L), and in one of them GH secretion became normal 1 yr after pituitary irradiation. Thus, preoperative administration of SMS 201-995 consistently induced shrinkage of GH-producing pituitary tumors, and the apparent remission rate was high in the treated patients.
10例既往未接受过治疗的肢端肥大症合并侵袭性垂体大腺瘤患者,在经蝶窦或额下垂体腺瘤切除术前行长效生长抑素类似物SMS 201-995(山德士公司)治疗3至30周。术前,SMS 201-995治疗使8例患者的24小时平均血浆生长激素(GH)浓度从8.5 - 66.7降至4.6微克/升以下,其余2例患者降低60 - 80%。垂体肿瘤大小缩小20 - 54%。形态学上,肿瘤显示总细胞、细胞质和细胞核面积减小;不同程度的血管周围纤维化;以及致密颗粒状。术后,8例患者的血浆GH和胰岛素样生长因子I浓度降至正常范围,GH动态变化恢复正常。其余2例患者术后仍存在轻度GH分泌过多(空腹和随机血浆GH平均浓度分别为6.1和7.9微克/升),其中1例在垂体放疗1年后GH分泌恢复正常。因此,术前给予SMS 201-995能持续诱导产生GH的垂体肿瘤缩小,且治疗患者的明显缓解率较高。