Ron I G, Soyfer V, Goldray D, Inbar M J, Weisman Y
Department of Oncology, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, 6 Weizmann Street, 64239, Tel Aviv, Israel.
Eur J Cancer. 2002 Jul;38(11):1490-4. doi: 10.1016/s0959-8049(02)00077-1.
Megestrol acetate (MA) has glucocorticoid activity and can induce significant secondary adrenal suppression. We designed this study to determine the extent of adrenal insufficiency in cancer patients receiving MA by utilising a sensitive low-dose adrenocorticotropin (ACTH) stimulation test. Adrenal function was assessed by a low-dose (0.625 microg) ACTH (1-24) stimulation test in 30 patients receiving MA for metastatic cancer. 10 of the patients who failed this test underwent a standard (250 microg) test on another day. Adrenal function was also evaluated in 15 of the patients by measuring the excretion of free cortisol in 24-h urine samples. Peak serum cortisol levels following stimulation with low-dose (0.625 microg) ACTH (1-24) were <18 microg/dl in 16 of 30 (53%) patients, of whom 9 had a basal serum cortisol level of <5 microg/dl. Five of 16 poor responders to the low-dose test showed normal stimulation with the standard (250 microg) ACTH (1-24) test. Thus, adrenal insufficiency would fail to be detected by the standard high dose test in these patients. Patients who failed the low-dose ACTH (1-24) test had lower 24-h urinary free cortisol excretion (8.7+/-10.3 microg/24 h) than normal responders (35+/-12.7 microg/24 h). Impaired adrenal function is common in cancer patients receiving MA. The low-dose ACTH (1-24) test is apparently capable of revealing adrenal insufficiency undetected by the standard high-dose ACTH test. Patients receiving MA might have inadequate adrenal function during episodes of infection or after withdrawal of MA therapy and this may require prompt corticosteroid treatment.
醋酸甲地孕酮(MA)具有糖皮质激素活性,可引起显著的继发性肾上腺抑制。我们设计了这项研究,通过使用敏感的低剂量促肾上腺皮质激素(ACTH)刺激试验来确定接受MA治疗的癌症患者肾上腺功能不全的程度。对30例接受MA治疗转移性癌症的患者进行了低剂量(0.625微克)促肾上腺皮质激素(1 - 24)刺激试验以评估肾上腺功能。其中10例该试验未通过的患者在另一天进行了标准剂量(250微克)试验。还通过测量24小时尿样中游离皮质醇的排泄量对15例患者的肾上腺功能进行了评估。30例患者中有16例(53%)在接受低剂量(0.625微克)促肾上腺皮质激素(1 - 24)刺激后血清皮质醇峰值水平<18微克/分升,其中9例基础血清皮质醇水平<5微克/分升。16例低剂量试验反应不佳的患者中有5例在标准剂量(250微克)促肾上腺皮质激素(1 - 24)试验中显示刺激反应正常。因此,在这些患者中,标准高剂量试验无法检测到肾上腺功能不全。低剂量促肾上腺皮质激素(1 - 24)试验未通过的患者24小时尿游离皮质醇排泄量(8.7±10.3微克/24小时)低于正常反应者(35±12.7微克/24小时)。接受MA治疗的癌症患者肾上腺功能受损很常见。低剂量促肾上腺皮质激素(1 - 24)试验显然能够发现标准高剂量促肾上腺皮质激素试验未检测到的肾上腺功能不全。接受MA治疗的患者在感染期间或MA治疗停药后可能肾上腺功能不足,这可能需要及时进行皮质类固醇治疗。