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应用抗酒石酸酸性磷酸酶治疗肿瘤诱导的骨溶解。

Treatment of tumor-induced osteolysis by APD.

作者信息

Burckhardt P, Thiébaud D, Perey L, von Fliedner V

机构信息

Departement für Innere Medizin, Universitätsklinik CHUV, Lausanne, Switzerland.

出版信息

Recent Results Cancer Res. 1989;116:54-66. doi: 10.1007/978-3-642-83668-8_5.

Abstract

Bisphosphonates, associated with rehydration, became the treatment of choice of malignant hypercalcemia when it became apparent that these compounds normalized plasma calcium in most cases within a few days and with almost no side effects, and that their effect was prolonged. Dichloromethylene bisphosphonate and aminobisphosphonate, especially APD, were shown to inhibit bone resorption with no noticeable inhibition of bone formation, and were highly effective in the long-term treatment of Paget's disease. APD was used in almost 300 patients with malignant hypercalcemia published in the literature and has been used in the medical clinic at Lausanne for several years. When given to 14 patients with malignant hypercalcemia at the dose of 25 mg/day until plasma calcium became normal for two consecutive days, APD had to be given for 4-11 days, severe hypercalcemia needing longer treatment than mild hypercalcemia (Adami et al. 1982). When given for a fixed period of 6 days, again plasma calcium normalized in all patients, whether APD was given i.v. (30 mg/day, ten patients) or orally (1200 mg/day, ten patients) (Adami et al. 1985). Further shortening of the treatment to one single infusion given over 24 h did not decrease the efficacy, as long as high enough doses were given (Blomqvist 1986). For severe hypercalcemia of above 3.5 mmol/liter 60-90 mg had to be given, while 30-45 mg was sufficient in milder cases (Body 1984). Otherwise, mild, transient, and asymptomatic hypocalcemia could occur. Normalization of plasma calcium went along with clinical improvement, sometimes even with correction of coma. Renal function was improved, even when the initial plasma creatinine levels were up to twice normal. Hypercalcemia could reoccur, but the duration of the effect of APD (1 week to several months) depended among other things on the dose administered. The decrease in plasma calcium was accompanied by a decrease in urinary calcium and hydroxyproline, both showing inhibition of bone resorption. In the case of recurrency, the treatment could be repeated with almost unaltered efficacy, except in end-stage cancer disease. When given to 13 normocalcemic patients with bone metastases from breast cancer, hydroxyproline and urinary calcium again decreased. Bone pains and radiologic signs of metastatic bone resorption also showed significant improvement, although these latter effects could also be explained by the antitumoral treatment, in this uncontrolled open trial.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

双膦酸盐与补液相关,当发现这些化合物在大多数情况下能在几天内使血钙正常化且几乎无副作用,且其效果持久时,双膦酸盐成为恶性高钙血症的首选治疗方法。二氯亚甲基双膦酸盐和氨基双膦酸盐,尤其是阿仑膦酸钠(APD),被证明能抑制骨吸收而对骨形成无明显抑制作用,并且在佩吉特病的长期治疗中非常有效。文献中报道了近300例使用APD治疗恶性高钙血症的患者,并且它已在洛桑的诊所使用了数年。当以25毫克/天的剂量给予14例恶性高钙血症患者,直至血钙连续两天正常时,APD需要给药4 - 11天,重度高钙血症比轻度高钙血症需要更长的治疗时间(阿达米等人,1982年)。当给予固定的6天疗程时,无论APD是静脉注射(30毫克/天,10例患者)还是口服(1200毫克/天,10例患者),所有患者的血钙均恢复正常(阿达米等人,1985年)。只要给予足够高的剂量,将治疗进一步缩短至单次24小时输注并不降低疗效(布洛姆奎斯特,1986年)。对于血钙高于3.5毫摩尔/升的重度高钙血症患者,必须给予60 - 9

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