Tamoxifen and its main metabolites serum and tissue concentrations in breast cancer women

被引:32
作者
Furlanut, Mario
Franceschi, Loretta
Pasqual, Enrico
Bacchetti, Stefano
Poz, Donatella
Giorda, Giorgio
Cagol, PierPaolo
机构
[1] Univ Udine, Inst Clin Pharmacol & Toxicol, DPMSC, I-33100 Udine, Italy
[2] Univ Udine, Chair Semeiot Chirurg, I-33100 Udine, Italy
[3] Croatian Acad Sci & Arts, Div Gynecol Oncol, Aviano, Italy
关键词
tamoxifen; active metabolites; tissue concentrations; breast cancer;
D O I
10.1097/FTD.0b013e318067ded7
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 [基础医学];
摘要
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 I month of continuous treatment, with desmethyltarnoxifen 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 lymphnodes, 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).
引用
收藏
页码:349 / 352
页数:4
相关论文
共 15 条
[1]
Ion suppression in mass spectrometry [J].
Annesley, TM .
CLINICAL CHEMISTRY, 2003, 49 (07) :1041-1044
[2]
COMPARATIVE BINDING AFFINITIES OF TAMOXIFEN, 4-HYDROXYTAMOXIFEN, AND DESMETHYLTAMOXIFEN FOR ESTROGEN-RECEPTORS ISOLATED FROM HUMAN-BREAST CARCINOMA - CORRELATION WITH BLOOD-LEVELS IN PATIENTS WITH METASTATIC BREAST-CANCER [J].
FABIAN, C ;
TILZER, L ;
STERNSON, L .
BIOPHARMACEUTICS & DRUG DISPOSITION, 1981, 2 (04) :381-390
[3]
QUANTITATIVE MEASUREMENT OF 4-HYDROXY TAMOXIFEN IN HUMAN PLASMA AND MAMMARY-TUMORS BY COMBINED GAS-CHROMATOGRAPHY NEGATIVE CHEMICAL-IONIZATION MASS-SPECTROMETRY [J].
GIRAULT, J ;
ISTIN, B ;
FOURTILLAN, JB .
BIOLOGICAL MASS SPECTROMETRY, 1993, 22 (07) :395-402
[4]
MONOHYDROXYLATED METABOLITE OF TAMOXIFEN WITH POTENT ANTI-ESTROGENIC ACTIVITY [J].
JORDAN, VC ;
COLLINS, MM ;
ROWSBY, L ;
PRESTWICH, G .
JOURNAL OF ENDOCRINOLOGY, 1977, 75 (02) :305-316
[5]
LONG-TERM ADJUVANT TAMOXIFEN THERAPY FOR BREAST-CANCER [J].
JORDAN, VC .
BREAST CANCER RESEARCH AND TREATMENT, 1990, 15 (03) :125-136
[6]
EFFECTS OF TAMOXIFEN ON UTERUS AND OVARIES OF POSTMENOPAUSAL WOMEN IN A RANDOMIZED BREAST-CANCER PREVENTION TRIAL [J].
KEDAR, RP ;
BOURNE, TH ;
POWLES, TJ ;
COLLINS, WP ;
ASHLEY, SE ;
COSGROVE, DO ;
CAMPBELL, S .
LANCET, 1994, 343 (8909) :1318-1321
[7]
TAMOXIFEN METABOLITES IN PATIENTS ON LONG-TERM ADJUVANT THERAPY FOR BREAST-CANCER [J].
LANGANFAHEY, SM ;
TORMEY, DC ;
JORDAN, VC .
EUROPEAN JOURNAL OF CANCER, 1990, 26 (08) :883-888
[8]
LIEN EA, 1991, CANCER RES, V51, P4837
[9]
Identification and mechanism of formation of potentially genotoxic metabolites of tamoxifen: Study by LC-MS/MS [J].
Lim, CK ;
Yuan, ZX ;
Jones, RM ;
White, INH ;
Smith, LL .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1997, 15 (9-10) :1335-1342
[10]
Endoxifen (4-hydroxy-N-desmethyl-tamoxifen) has anti-estrogenic effects in breast cancer cells with potency similar to 4-hydroxy-tamoxifen [J].
Lim, YC ;
Desta, Z ;
Flockhart, DA ;
Skaar, TC .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2005, 55 (05) :471-478