Tsagarakis S, Grossman A, Plowman P N, Jones A E, Touzel R, Rees L H, Wass J A, Besser G M
Department of Endocrinology, St Bartholomew's Hospital, London, UK.
Clin Endocrinol (Oxf). 1991 May;34(5):399-406. doi: 10.1111/j.1365-2265.1991.tb00312.x.
OBJECTIVE To determine the long-term effects of external beam megavoltage radiotherapy (RT: 4500 cGy via three portals at 180 cGy or less total daily dose) on endocrine function in prolactinomas. DESIGN Longitudinal study following radiotherapy with periodic re-assessment at regular intervals, at least 2 months off dopamine agonist therapy. PATIENTS Thirty-six female patients, age range 19-50 years, with either macroprolactinomas (12 patients) or microprolactinomas (24 patients), but without significant suprasellar extensions. MEASUREMENTS Clinical appraisal, and anterior and posterior pituitary assessment: basal levels at yearly intervals or less, with dynamic screening with TRH, LHRH and hypoglycaemic stimulation every 2-3 years. RESULTS Before RT, serum prolactin (PRL) levels ranged from 1150 to 34,000 mU/l; after RT (mean 8.5 years, range 3-14), serum PRL fell to normal (i.e. less than 360 mU/l) in 18 of the 36 patients (50%), and to just above the normal range (378-780 mU/l) in a further 10 (28%). Two patients had PRL levels at their last follow-up higher than those at presentation, with one patient showing evidence of tumour recurrence on CT scan. A total of eight of the 36 patients (23%) developed post-RT gonadal deficiency by the end of follow-up at 8 +/- 3.1 years (+/- SD, range 3-11), but six were aged over 40 years at that time. GH deficiency was frequent, occurring in 94% of patients, usually from 2 to 3 years post-RT, while TSH deficiency and reduced ACTH reserve was uncommon (each 14%), and occurred later. In the subgroup of 12 patients with macroprolactinomas, results were broadly comparable. CONCLUSIONS Megavoltage RT produces a progressive fall in serum prolactin in the great majority of patients with prolactinomas, with a relatively low incidence of TSH or ACTH deficiency. As it is now clear that dopamine agonist therapy alone provides sufficient management for microprolactinomas, RT may be used for the long-term control of macroprolactinomas, together with interim dopamine agonist therapy. It allows pregnancy to be safely undertaken but, in view of the delayed onset of gonadal deficiency, its administration should be timed with respect to the desired onset of conception in women.
目的 确定外照射兆伏级放疗(放疗:通过三个射野给予4500厘戈瑞,每日总剂量180厘戈瑞或更低)对催乳素瘤内分泌功能的长期影响。 设计 放疗后的纵向研究,定期进行重新评估,多巴胺激动剂治疗至少中断2个月。 患者 36例女性患者,年龄19 - 50岁,患有大催乳素瘤(12例)或微催乳素瘤(24例),但无明显鞍上扩展。 测量 临床评估以及垂体前叶和后叶评估:每年或更短时间间隔测量基础水平,每2 - 3年进行促甲状腺激素释放激素(TRH)、促黄体生成素释放激素(LHRH)和低血糖刺激的动态筛查。 结果 放疗前,血清催乳素(PRL)水平为1150至34000 mU/l;放疗后(平均8.5年,范围3 - 14年),36例患者中有18例(50%)血清PRL降至正常(即低于360 mU/l),另有10例(28%)降至略高于正常范围(378 - 780 mU/l)。2例患者在最后一次随访时PRL水平高于初诊时,1例患者CT扫描显示有肿瘤复发迹象。36例患者中有8例(23%)在8±3.1年(±标准差,范围3 - 11年)的随访结束时出现放疗后性腺功能减退,但其中6例当时年龄超过40岁。生长激素(GH)缺乏很常见,94%的患者出现,通常在放疗后2至3年,而促甲状腺激素(TSH)缺乏和促肾上腺皮质激素(ACTH)储备减少不常见(各14%),且出现较晚。在12例大催乳素瘤患者亚组中,结果大致相似。 结论 兆伏级放疗使大多数催乳素瘤患者血清催乳素逐渐下降,TSH或ACTH缺乏发生率相对较低。由于现在很清楚单独使用多巴胺激动剂治疗对微催乳素瘤就足够了,放疗可用于大催乳素瘤的长期控制,同时联合临时多巴胺激动剂治疗。它允许安全怀孕,但鉴于性腺功能减退发病延迟,其应用应根据女性期望的受孕时间来安排。