Neuroendocrine Unit, Massachusetts General Hospital. Department of Medicine, Harvard Medical School, Boston, MA.
Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
J Clin Endocrinol Metab. 2020 Mar 1;105(3):e532-43. doi: 10.1210/clinem/dgz187.
To determine the prevalence of insulin-like growth factor-1 (IGF-1) normalization with long-term multimodality therapy in a pituitary center and to assess changes over time.
Patients with acromegaly (N = 409), with ≥1 year of data after surgery and at least 2 subsequent clinic visits were included in long-term analysis (N = 266). Biochemical data, clinical characteristics, and therapeutic interventions were reviewed retrospectively.
At diagnosis, mean [standard deviation] age was 43.4 [14.3] years, body mass index was 28.5 (24.9-32.1) kg/m2 (median, interquartile range), serum IGF-1 index (IGF-1 level/upper limit of normal) was 2.3 [1.7-3.1], and 80.5% had macroadenomas. Patients with transsphenoidal surgery after 2006 were older [46.6 ± 14.3 vs 40.0 ± 13.4 years; P < 0.001]. Age and tumor size correlated inversely. Overall (N = 266), 93.2% achieved a normal IGF-1 level during 9.9 [5.0-15.0] years with multimodality therapy. The interval to first normal IGF-1 level following failed surgical remission was shorter after 2006: 14.0 (95% confidence interval, 10.0-20.0) versus 27.5 (22.0-36.0) months (P = 0.002). Radiation therapy and second surgery were rarer after 2006: 28 (22%) versus 62 (47.0%); P < 0.001 and 12 (9.4%) versus 28 (21.2%); P = 0.010, respectively. Age at diagnosis increased over time periods, possibly reflecting increased detection of acromegaly in older patients with milder disease. Male gender, older age, smaller tumor and lower IGF-1 index at diagnosis predicted long-term sustained IGF-1 control after surgery without adjuvant therapies.
The vast majority of patients with acromegaly can be biochemically controlled with multimodality therapy in the current era. Radiotherapy and repeat pituitary surgery became less frequently utilized over time. Long-term postoperative IGF-1 control without use of adjuvant therapies has improved.
确定长期多模式治疗在垂体中心使胰岛素样生长因子-1(IGF-1)正常化的患病率,并评估随时间的变化。
纳入了术后至少 1 年且至少有 2 次后续就诊的 409 例肢端肥大症患者进行长期分析(n=266)。回顾性审查了生化数据、临床特征和治疗干预措施。
诊断时,患者的平均[标准差]年龄为 43.4[14.3]岁,体重指数为 28.5(24.9-32.1)kg/m2(中位数,四分位间距),血清 IGF-1 指数(IGF-1 水平/正常上限)为 2.3[1.7-3.1],80.5%有大腺瘤。2006 年后接受经蝶窦手术的患者年龄较大[46.6±14.3 岁比 40.0±13.4 岁;P<0.001]。年龄与肿瘤大小呈负相关。在整个(n=266)患者中,93.2%在 9.9[5.0-15.0]年的多模式治疗期间达到 IGF-1 水平正常。在手术缓解失败后首次 IGF-1 水平正常的时间间隔在 2006 年后更短:14.0(95%置信区间,10.0-20.0)个月比 27.5(22.0-36.0)个月(P=0.002)。2006 年后,放射治疗和二次手术的比例较低:28(22%)比 62(47.0%)(P<0.001)和 12(9.4%)比 28(21.2%)(P=0.010)。诊断时的年龄随时间推移而增加,这可能反映出随着疾病的轻微进展,年龄较大的肢端肥大症患者的检出率增加。男性、年龄较大、肿瘤较小和诊断时 IGF-1 指数较低,预测术后无需辅助治疗即可长期维持 IGF-1 控制。
在当前时代,大多数肢端肥大症患者可以通过多模式治疗实现生化控制。放射治疗和重复垂体手术的应用频率随时间推移而降低。长期术后无需辅助治疗即可控制 IGF-1,且控制情况有所改善。