Department of Endocrinology, Seth G.S. Medical College & King Edward Memorial Hospital, Mumbai, India.
Department of Endocrinology, Vydehi Institute of Medical Sciences, Research Centre, Bangalore, India.
Ann Endocrinol (Paris). 2023 Dec;84(6):711-718. doi: 10.1016/j.ando.2023.10.005. Epub 2023 Oct 20.
Giant prolactinomas (GP) are rare tumors accounting for 4.3% of prolactinomas, with paucity of literature from India. We aim to describe clinical, biochemical, radiological, and treatment outcomes in a large series of Asian-Indian patients with GP.
A single-center retrospective analysis of GPs (n=84), age-based (adults: 66 versus pediatric: 18) and gender-based (males: 64 versus females: 20) comparison was done.
The mean age at presentation was 34.1±13years, and 64 (76.2%) were males. Males were younger at presentation (32.1±12.2 versus 40.1±13.8years, P: 0.01). The majority presented with mass-effect-related manifestations (visual disturbances: 91.6%, headache: 84.5%) and/or hypogonadism (98.7%). At baseline, largest tumor dimension was 5.3±1.0cm, and serum prolactin was 8343 (3865.5-12,306) ng/mL; most (94.6%) had gonadal axis involvement. Dopamine-agonist (DA) as first-line therapy (45/67, 67.2%) achieved normoprolactinemia (maximum cabergoline dose: 2.0±1.2mg/week) in 36/45 (80%) and tumor response (≥50% reduction) in 36/37 (97.3%) patients at the last follow-up (median duration: 33 [14.5-53.5]months). Notably, gonadal axis recovery was poor (6/30, 20%) despite normoprolactinemia post-DA monotherapy. At latest follow-up, secondary hypothyroidism (32.5% versus 82.6%, P: 0.001) and central hypocortisolism (5.6% versus 42.9%, P: 0.007) were less frequent in DA monotherapy (n=43) than in multimodal therapy group (n=23). The proportion of males (94.4% versus 71.2%, P: 0.04) was higher in the pediatric age group, with DA-induced (first-line) normoprolactinemia observed in 66.7% of them.
GP has male predominance, DA as first-line therapy normalized prolactin in four-fifths of patients with better preservation of HPT and HPA axes in patients with DA monotherapy.
巨大泌乳素瘤(GP)是一种罕见的肿瘤,占泌乳素瘤的 4.3%,印度的文献资料很少。我们旨在描述一组来自亚洲印度的 GP 患者的临床、生化、影像学和治疗结果。
对 84 例 GP 患者(按年龄分为成年组:66 例和儿童组:18 例;按性别分为男性组:64 例和女性组:20 例)进行单中心回顾性分析。
患者的平均发病年龄为 34.1±13 岁,64 例(76.2%)为男性。男性患者的发病年龄更小(32.1±12.2 岁 vs. 40.1±13.8 岁,P:0.01)。大多数患者表现为肿块效应相关症状(视力障碍:91.6%,头痛:84.5%)和/或性腺功能减退(98.7%)。基线时,最大肿瘤直径为 5.3±1.0cm,血清泌乳素为 8343(3865.5-12306)ng/ml;大多数(94.6%)患者存在性腺轴受累。多巴胺激动剂(DA)作为一线治疗(45/67,67.2%),在最后一次随访时,45 例中的 36 例(80%)实现了正常泌乳素水平(最大卡麦角林剂量:2.0±1.2mg/周),37 例中的 36 例(97.3%)实现了肿瘤反应(≥50%缩小)(中位随访时间:33 [14.5-53.5]个月)。值得注意的是,尽管 DA 单药治疗后泌乳素水平正常,但性腺轴恢复情况较差(6/30,20%)。在最新的随访中,DA 单药治疗组(n=43)的继发性甲状腺功能减退症(32.5% vs. 82.6%,P:0.001)和中枢性皮质醇功能减退症(5.6% vs. 42.9%,P:0.007)的发生率低于多模式治疗组(n=23)。在儿童组中,男性比例(94.4% vs. 71.2%,P:0.04)更高,其中 66.7%的患者接受 DA 诱导(一线)正常泌乳素水平治疗。
GP 以男性为主,DA 作为一线治疗,使五分之四的患者的泌乳素恢复正常,DA 单药治疗在 HPT 和 HPA 轴的保护方面更好。