Furlanut Mario, Franceschi Loretta, Pasqual Enrico, Bacchetti Stefano, Poz Donatella, Giorda Giorgio, Cagol Pierpaolo
Institute of Clinical Pharmacology and Toxicology, DPMSC, University of Udine, Udine, Italy.
Ther Drug Monit. 2007 Jun;29(3):349-52. doi: 10.1097/FTD.0b013e318067ded7.
Because of a possible relationship between tamoxifen (T) concentrations and clinical effects, we initiated a preliminary investigation on serum and tissue concentrations of T and its main active metabolites, and 4-hydroxytamoxifen, in women with positive breast cancer estrogen receptor. One hundred forty-eight patients were studied: 80 were admitted for monitoring of therapeutic serum drug concentrations, 22 had tissue concentrations taken at surgery, and 46 patients had uterine mucosa levels measured at diagnostic hysteroscopy. Steady-state serum concentrations were reached after 1 month of continuous treatment, with desmethyltamoxifen being the highest represented derivative from the third week onward. There was no relationship between dose (in mg/kg body weight) and steady-state serum concentrations during therapeutic drug monitoring of patients. The highest tissue concentrations were observed in breast lymph-nodes, cancer tissue, and uterine mucosa. On the basis of these data, we speculate that T and its active metabolites may exert both a defensive role (ie, an obstacle to the diffusion of malignant cells through the local lymphatic system) and a harmful one (induction of uterine malignancies).
由于他莫昔芬(T)浓度与临床疗效之间可能存在关联,我们对雌激素受体阳性乳腺癌女性患者的血清和组织中T及其主要活性代谢产物4-羟基他莫昔芬的浓度展开了初步研究。共研究了148例患者:80例因监测治疗性血清药物浓度而入院,22例在手术时测定了组织浓度,46例患者在诊断性宫腔镜检查时测定了子宫黏膜水平。连续治疗1个月后达到稳态血清浓度,从第三周起,去甲基他莫昔芬是含量最高的衍生物。在患者治疗药物监测期间,剂量(mg/kg体重)与稳态血清浓度之间无关联。在乳腺淋巴结、癌组织和子宫黏膜中观察到最高的组织浓度。基于这些数据,我们推测T及其活性代谢产物可能发挥防御作用(即阻碍恶性细胞通过局部淋巴系统扩散)和有害作用(诱发子宫恶性肿瘤)。