Kisanga Elton R, Gjerde Jennifer, Guerrieri-Gonzaga Aliana, Pigatto Francesca, Pesci-Feltri Adriana, Robertson Chris, Serrano Davide, Pelosi Giuseppe, Decensi Andrea, Lien Ernst A
Hormone Laboratory, Haukeland University Hospital, Department of Medicine, and Centre for International Health, University of Bergen, Bergen, Norway.
Clin Cancer Res. 2004 Apr 1;10(7):2336-43. doi: 10.1158/1078-0432.ccr-03-0538.
Both therapeutic and adverse effects of tamoxifen may be related to its tissue concentrations. We investigated concentrations of tamoxifen, 4-hydroxytamoxifen, N-desmethyltamoxifen, and N-didesmethyltamoxifen in serum, normal breast, and breast cancer tissues during conventional dosage and two low-dose regimens. Furthermore we studied tamoxifen effects on the cancer proliferation marker Ki-67, and on sex hormone-binding globulin (SHBG).
From September 1999 to August 2001, 120 breast cancer patients were randomized to 20-, 5-, or 1-mg tamoxifen daily. We measured serum and tissue concentrations of tamoxifen and three metabolites after 28 days of treatment, and the changes between baseline and post-treatment levels of SHBG and Ki-67.
The median (range) tamoxifen concentrations (ng/ml) at doses of 1, 5, and 20 mg daily (n = 38, 37, and 36) were 7.5 (2.9-120.9), 25.2 (1.9-180.9), and 83.6 (8.7-134.4) in serum, and 78.2 (35.9-184), 272.3 (122-641), and 744.4 (208.6-2556) in breast cancer tissue, respectively. Tamoxifen levels followed a dose-concentration relationship. The concentrations of tamoxifen and metabolites were related to each other. Serum and tissue concentrations of tamoxifen were associated with corresponding changes of SHBG levels, whereas changes of Ki-67 levels were not related.
Estrogen agonistic effects of tamoxifen on SHBG decreased with lower dosage, whereas tamoxifen effects on Ki-67 expression did not change. This together with a >10-fold variation in serum tamoxifen concentrations and a serum to tissue concentration relationship suggest that tamoxifen treatment may be improved by administration of lower doses and therapeutic drug monitoring.
他莫昔芬的治疗作用和不良反应可能都与其组织浓度有关。我们研究了在常规剂量及两种低剂量方案下,血清、正常乳腺组织及乳腺癌组织中他莫昔芬、4-羟基他莫昔芬、N-去甲基他莫昔芬和N-双去甲基他莫昔芬的浓度。此外,我们还研究了他莫昔芬对癌症增殖标志物Ki-67以及性激素结合球蛋白(SHBG)的影响。
1999年9月至2001年8月,120例乳腺癌患者被随机分为每日服用20毫克、5毫克或1毫克他莫昔芬三组。治疗28天后,我们测量了血清和组织中他莫昔芬及三种代谢物的浓度,以及SHBG和Ki-67在基线水平和治疗后水平的变化。
每日剂量为1毫克、5毫克和20毫克(n分别为38、37和36)时,他莫昔芬的中位(范围)浓度(纳克/毫升)在血清中分别为7.5(2.9 - 120.9)、25.2(1.9 - 180.9)和83.6(8.7 - 134.4),在乳腺癌组织中分别为78.2(35.9 - 184)、272.3(122 - 641)和744.4(208.6 - 2556)。他莫昔芬水平呈现剂量 - 浓度关系。他莫昔芬及其代谢物的浓度相互关联。他莫昔芬的血清和组织浓度与SHBG水平的相应变化相关,而与Ki-67水平的变化无关。
他莫昔芬对SHBG的雌激素激动作用随剂量降低而减弱,而他莫昔芬对Ki-67表达的影响不变。这与血清中他莫昔芬浓度超过10倍的变化以及血清与组织浓度关系表明,通过给予较低剂量和进行治疗药物监测可能会改善他莫昔芬的治疗效果。