EFFECT OF THE NEW DOPAMINERGIC AGONIST CV 205-502 ON PLASMA PROLACTIN LEVELS AND TUMOR SIZE IN BROMOCRIPTINE-RESISTANT PROLACTINOMAS

被引:52
作者
DURANTEAU, L
CHANSON, P
LAVOINNE, A
HORLAIT, S
LUBETZKI, J
KUHN, JM
机构
[1] HOP CHARLES NICOLLE,SERV BIOCHIM,F-76031 ROUEN,FRANCE
[2] HOP LARIBOISIERE,SERV MED INTERNE & ENDOCRINOL,F-75475 PARIS 10,FRANCE
[3] LABS SANDOZ FRANCE,F-92500 RUEIL-MALMAISON,FRANCE
关键词
D O I
10.1111/j.1365-2265.1991.tb01731.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bromocriptine is currently and successfully used for the treatment of pituitary prolactinomas. However, bromocriptine appears unable to normalize plasma prolactin levels in about 10% and to reduce tumour size in one-third of cases. The lack of normalization of plasma prolactin levels in spite of a daily dose of bromocriptine equal to or higher than 15 mg suggests a bromocriptine resistance. We compared the long-term effects of bromocriptine and CV 205-502 (a non-ergot derivative D2 dopamine agonist) on plasma prolactin levels and tumour size in seven bromocriptine-resistant prolactinomas. Bromocriptine reduced significantly (P < 0.001) plasma prolactin levels (from 2307 +/- 518 to 568 +/- 279-mu-g/1) (conversion to Sl units: 1-mu-g/1 = 20 mU/1). Visual field defects observed in five patients improved in four. However, CT scan analysis showed a decrease in tumour size in only three patients. Except for transient and minor side-effects at the beginning of the treatment, CV 205-502 was well tolerated in five of seven patients. In the remaining two patients nausea and vertigo occurred with high dosages of CV 205-502 and it was necessary to reduce the daily dose. CV 205-502 lowered plasma prolactin to levels similar to those obtained after bromocriptine therapy in four cases. In the three remaining patients, CV 205-502 was more potent than bromocriptine as demonstrated by the further 90% reduction in plasma levels obtained in one case and by the normalization of plasma prolactin levels in the two other cases. One woman became pregnant during CV 205-502 treatment. However, no further change in visual disturbance or in tumour size was observed during the treatment with CV 205-502. These results show that CV 205-502 appears to be more potent than bromocriptine in reducing plasma prolactin levels in some bromocriptine-resistant prolactinomas and suggest that different mechanisms may be involved in such a resistance.
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页码:25 / 29
页数:5
相关论文
共 18 条
[11]   RESISTANCE TO BROMOCRIPTINE IN PROLACTINOMAS [J].
PELLEGRINI, I ;
RASOLONJANAHARY, R ;
GUNZ, G ;
BERTRAND, P ;
DELIVET, S ;
JEDYNAK, CP ;
KORDON, C ;
PEILLON, F ;
JAQUET, P ;
ENJALBERT, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 69 (03) :500-509
[12]   LONG-TERM TREATMENT WITH A NEW NON-ERGOT LONG-ACTING DOPAMINE AGONIST, CV-205-502, IN WOMEN WITH HYPERPROLACTINEMIA [J].
RASMUSSEN, C ;
BERGH, T ;
WIDE, L ;
BROWNELL, J .
CLINICAL ENDOCRINOLOGY, 1988, 29 (03) :271-279
[13]   RAPID REGRESSION OF PITUITARY PROLACTINOMAS DURING BROMOCRIPTINE TREATMENT [J].
THORNER, MO ;
MARTIN, WH ;
ROGOL, AD ;
MORRIS, JL ;
PERRYMAN, RL ;
CONWAY, BP ;
HOWARDS, SS ;
WOLFMAN, MG ;
MACLEOD, RM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1980, 51 (03) :438-445
[14]  
THORNER MO, 1978, ACTA ENDOCRINOL-COP, V88, P131
[15]   CV 205-502 TREATMENT OF HYPERPROLACTINEMIA [J].
VANCE, ML ;
CRAGUN, JR ;
REIMNITZ, C ;
CHANG, RJ ;
RASHEF, E ;
BLACKWELL, RE ;
MILLER, MM ;
MOLITCH, ME .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 68 (02) :336-339
[16]  
WANG C, 1989, 2ND INT PIT C PALM S, pM1
[17]  
WASS JA, BRIT MED J, V284, P1908
[18]  
WERDER KV, 1978, J ENDOCRINOL INVEST, V1, P47