Watanabe Shinya, Akutsu Hiroyoshi, Takano Shingo, Yamamoto Tetsuya, Ishikawa Eiichi, Suzuki Hiroaki, Matsumura Akira
Department of Neurosurgery, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Division of Endocrinology and Metabolism, Department of Internal Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Clin Endocrinol (Oxf). 2017 Feb;86(2):207-213. doi: 10.1111/cen.13240. Epub 2016 Oct 11.
Withdrawal of cabergoline is generally challenging, especially in patients with large or invasive macroprolactinomas. Therefore, we aimed to assess long-term results of cabergoline therapy for macroprolactinomas and remission achievement results after withdrawal in patients with macroprolactinomas. We also investigated clinical characteristics and factors related to remission after withdrawal.
This was an institutional review board-approved retrospective analysis. We studied 46 macroprolactinoma patients who had taken cabergoline during the period from 2003 through 2013. Administration of cabergoline was maintained for 5 years before withdrawal.
Median follow-up after the initiation of cabergoline therapy was 54·3 (range 5·3 to 137·2) months. Recurrences of hyperprolactinaemia were observed in 3 of 11 (27%) postwithdrawal patients at a median time of 3·0 (range; 2·9-11·2) months, indicating that a high percentage (73%) maintained remission for at least 12 months after cabergoline cessation. Factors significantly associated with remission were analysed in 21 patients receiving long-term cabergoline administration. On multivariate analysis, the absence of cavernous sinus invasion on pretreatment MRI (≥3/4 tumour encasement of the intracavernous internal carotid artery) (HR; 21·94, 95% CI; 2·06-1071·0, P = 0·006), initial PRL <132·7 ng/ml (HR; 8·28, 95% CI; 1·24-199·6, P = 0·03) and nadir PRL <1·9 ng/ml during cabergoline therapy (HR; 5·14, 95% CI; 1·10-39·02, P = 0·04) showed statistically significant correlations with remission after withdrawal.
Cabergoline therapy can achieve a high percentage (73% in this series) of remission maintenance for at least 12 months after cessation of a 5-year course of therapy, even in patients with macroprolactinomas. The absence of cavernous sinus invasion, serum PRL level lower than 132·7 ng/ml before cabergoline therapy or nadir serum PRL below 1·9 ng/ml were related to more frequent remission after withdrawal of cabergoline in patients receiving this medication for 5 years.
停用卡麦角林通常具有挑战性,尤其是对于患有大的或侵袭性泌乳素瘤的患者。因此,我们旨在评估卡麦角林治疗泌乳素瘤的长期效果以及泌乳素瘤患者停药后的缓解达成情况。我们还研究了停药后缓解的临床特征和相关因素。
这是一项经机构审查委员会批准的回顾性分析。我们研究了2003年至2013年期间服用卡麦角林的46例泌乳素瘤患者。在停药前,卡麦角林的给药维持了5年。
卡麦角林治疗开始后的中位随访时间为54.3(范围5.3至137.2)个月。11例停药后患者中有3例(27%)出现高泌乳素血症复发,中位复发时间为3.0(范围2.9至11.2)个月,这表明高比例(73%)的患者在停用卡麦角林后至少维持缓解12个月。对21例接受长期卡麦角林给药的患者分析了与缓解显著相关的因素。多因素分析显示,治疗前MRI未出现海绵窦侵袭(海绵窦内颈内动脉被肿瘤包绕≥3/4)(HR;21.94,95%CI;2.06至1071.0,P = 0.006)、初始泌乳素水平<132.7 ng/ml(HR;8.28,95%CI;1.24至199.6,P = 0.03)以及卡麦角林治疗期间最低泌乳素水平<1.9 ng/ml(HR;5.14,95%CI;1.10至39.02,P = 0.04)与停药后缓解在统计学上显著相关。
即使对于泌乳素瘤患者,卡麦角林治疗在5年疗程停止后,也能使高比例(本系列中为73%)的患者至少维持缓解12个月。未出现海绵窦侵袭、卡麦角林治疗前血清泌乳素水平低于132.7 ng/ml或最低血清泌乳素低于1.9 ng/ml与接受该药物治疗5年的患者停药后更频繁的缓解相关。