Reimondo Giuseppe, Puglisi Soraya, Zaggia Barbara, Basile Vittoria, Saba Laura, Perotti Paola, De Francia Silvia, Volante Marco, Zatelli Maria Chiara, Cannavò Salvatore, Terzolo Massimo
Internal Medicine 1Department of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.
Endocrine UnitDepartment of Clinical and Experimental Medicine, University of Messina, Messina, Italy
Eur J Endocrinol. 2017 Oct;177(4):361-367. doi: 10.1530/EJE-17-0452. Epub 2017 Aug 5.
Mitotane, a drug used to treat adrenocortical cancer (ACC), inhibits multiple enzymatic steps of adrenocortical steroid biosynthesis, potentially causing adrenal insufficiency. Recent studies have also documented a direct inhibitory effect of mitotane at the pituitary level. The present study was aimed to assess the hypothalamic-pituitary-adrenal axis in patients with ACC receiving mitotane.
We prospectively enrolled 16 patients on adjuvant treatment with mitotane after radical surgical resection of ACC, who underwent standard hormone evaluation and h-CRH stimulation. A group of 10 patients with primary adrenal insufficiency (PAI) served as controls for the CRH test.
We demonstrated a close correlation between cortisol-binding globulin (CBG) and plasma mitotane levels, and a non-significant trend between mitotane dose and either serum or salivary cortisol in ACC patients. We did not find any correlation between the dose of cortisone acetate and either ACTH or cortisol levels. ACTH levels were significantly higher in patients with PAI than that in patients with ACC, both in baseline conditions (88.99 (11.04-275.00) vs 24.53 (6.16-121.88) pmol/L, = 0.031) and following CRH (158.40 (34.32-275.00) vs 67.43 (8.8-179.52) pmol/L = 0.016).
The observation of lower ACTH levels in patients with ACC than that in patients with PAI, both in basal conditions and after CRH stimulation, suggests that mitotane may play an inhibitory effect on ACTH secretion at the pituitary levels. In conclusion, the present study shows that mitotane affects the HPA axis at multiple levels and no single biomarker may be used for the assessment of adrenal insufficiency.
米托坦是一种用于治疗肾上腺皮质癌(ACC)的药物,它能抑制肾上腺皮质类固醇生物合成的多个酶促步骤,有可能导致肾上腺功能不全。近期研究还记录了米托坦在垂体水平的直接抑制作用。本研究旨在评估接受米托坦治疗的ACC患者的下丘脑-垂体-肾上腺轴。
我们前瞻性纳入了16例ACC根治性手术切除后接受米托坦辅助治疗的患者,这些患者接受了标准激素评估和促肾上腺皮质激素释放激素(h-CRH)刺激试验。一组10例原发性肾上腺功能不全(PAI)患者作为CRH试验的对照。
我们发现皮质醇结合球蛋白(CBG)与血浆米托坦水平密切相关,且在ACC患者中米托坦剂量与血清或唾液皮质醇之间存在不显著的趋势。我们未发现醋酸可的松剂量与促肾上腺皮质激素(ACTH)或皮质醇水平之间存在任何相关性。PAI患者的ACTH水平在基线条件下(88.99(11.04 - 275.00)对24.53(6.16 - 121.88)pmol/L,P = 0.031)和CRH刺激后(158.40(34.32 - 275.00)对67.43(8.8 - 179.52)pmol/L,P = 0.016)均显著高于ACC患者。
在基础条件下和CRH刺激后,ACC患者的ACTH水平均低于PAI患者,这一观察结果表明米托坦可能在垂体水平对ACTH分泌起抑制作用。总之,本研究表明米托坦在多个水平影响下丘脑-垂体-肾上腺轴,且没有单一生物标志物可用于评估肾上腺功能不全。