PAMIDRONATE TREATMENT IN PATIENTS WITH TUMOR-ASSOCIATED HYPERCALCEMIA - PHARMACOLOGICAL EFFECTS AND PHARMACOKINETICS

被引:13
作者
OISO, Y
TOMITA, A
HASEGAWA, H
ARIYOSHI, Y
NIINOMI, M
YAMAMOTO, M
TAKANO, T
SAKIYAMA, N
机构
[1] AICHI MED UNIV,CENT LAB CLIN INVEST,NAGAKUTE,AICHI 48011,JAPAN
[2] JAPANESE RED CROSS,NAGOYA FIRST HOSP,NAGOYA,AICHI 453,JAPAN
[3] AICHI CANC CTR,NAGOYA,AICHI 464,JAPAN
[4] NAGOYA NATL HOSP,NAGOYA,AICHI 460,JAPAN
[5] ANJO KOSEI HOSP,ANJO 446,JAPAN
[6] CHUKYO HOSP,NAGOYA,AICHI 457,JAPAN
[7] CIBA GEIGY JAPAN LTD,PHARMACOKINET RES LAB,TAKARAZUKA,HYOGO 665,JAPAN
关键词
PAMIDRONATE; HYPERCALCEMIA; PTH RELATED PEPTIDE; PHARMACOKINETICS;
D O I
10.1507/endocrj.41.655
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The purpose of this study was to investigate the effects of pamidronate, a second generation bisphosphonate, on the change in calcium homeostasis in patients with tumor-associated hypercalcemia. Eight patients with tumor-associated hypercalcemia received intravenous infusion of pamidronate (45 mg) and their high mean serum calcium concentration significantly decreased from 3.56 mmol/L to 2.62 mmol/L 7 days after treatment. Serum intact PTH before treatment had been suppressed to below normal in all patients but returned to normal range in six patients within 7 days after treatment. Urinary PTH related peptide (PTHrP) excretion before treatment had been elevated in seven patients and then significantly increased further after pamidronate therapy. The serum bone Gla protein concentration was not apparently changed by the treatment. Pamidronate in serum was rapidly eliminated after the treatment and urinary excretion reached a plateau on the second day (13.8% of the administered dose), suggesting that the major portion of the infused dose had been distributed to the bone and other tissues. These findings suggest that pamidronate has a potent hypocalcemic effect and that PTHrP production in malignant tumors could be affected by pamidronate therapy.
引用
收藏
页码:655 / 661
页数:7
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