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比较不同剂量双膦酸盐伊班膦酸钠治疗恶性肿瘤高钙血症的随机II期试验。

Randomized phase II trial comparing different doses of the bisphosphonate ibandronate in the treatment of hypercalcemia of malignancy.

作者信息

Pecherstorfer M, Herrmann Z, Body J J, Manegold C, Degardin M, Clemens M R, Thürlimann B, Tubiana-Hulin M, Steinhauer E U, van Eijkeren M, Huss H J, Thiébaud D

机构信息

I. Department of Medicine and Medical Oncology, Wilhelminenspital, Vienna, Austria.

出版信息

J Clin Oncol. 1996 Jan;14(1):268-76. doi: 10.1200/JCO.1996.14.1.268.

Abstract

PURPOSE

To evaluate the hypocalcemic effect and safety of three different doses of the bisphosphonate ibandronate in tumor-associated hypercalcemia, and to identify factors predicting response.

PATIENTS AND METHODS

One hundred seventy-four cancer patients with a serum calcium level greater than 2.7 mmol/L (10.8 mg/dL) were enrolled onto the trial. If hypercalcemia persisted after fluid repletion, patients were randomly assigned to treatment with 0.6 mg, 1.1 mg, and 2.0 mg of ibandronate. Response, defined as restoration of normocalcemia, was evaluated by an intent-to-treat analysis.

RESULTS

One hundred seventy-three (99%) patients were assessable for toxicity and 151 (87%) for efficacy. The administration of 0.6 mg (group A), 1.1 mg (group B), or 2.0 mg (group C) of ibandronate led to response rates of 44%, 52%, and 67%, respectively. Significantly more patients in group C responded than in group A (P = .0276). Of the various parameters examined, only the initial serum calcium level (P < .0001; odds ratio, 0.083) and the dose of ibandronate (P = .0162; odds ratio, 2.094) correlated with response. One hundred ninety-five adverse events (AEs) were reported, 99 classified as serious and 96 as nonserious. Three serious and sixteen nonserious AEs were considered related to ibandronate treatment. The three serious AEs were one case with thrombocytopenia, one with nausea, and one with fever.

CONCLUSION

Ibandronate therapy led to a dose-dependent reduction in serum calcium levels. The response to ibandronate treatment correlated negatively with the initial serum calcium level and positively with the dose administered. A dose of 2 mg was necessary to achieve a response rate comparable to that in previous studies with the bisphosphonates pamidronate and clodronate. Because the incidence of drug-associated AEs was low, a dose escalation of ibandronate can be recommended for further clinical trials.

摘要

目的

评估三种不同剂量的双膦酸盐伊班膦酸钠对肿瘤相关性高钙血症的降钙作用及安全性,并确定预测反应的因素。

患者与方法

174例血清钙水平高于2.7 mmol/L(10.8 mg/dL)的癌症患者纳入该试验。如果补液后高钙血症持续存在,患者被随机分配接受0.6 mg、1.1 mg和2.0 mg伊班膦酸钠治疗。通过意向性分析评估定义为血钙恢复正常的反应。

结果

173例(99%)患者可评估毒性,151例(87%)可评估疗效。给予0.6 mg(A组)、1.1 mg(B组)或2.0 mg(C组)伊班膦酸钠后的反应率分别为44%、52%和67%。C组有反应的患者明显多于A组(P = 0.0276)。在检查的各种参数中,只有初始血清钙水平(P < 0.0001;比值比,0.083)和伊班膦酸钠剂量(P = 0.0162;比值比,2.094)与反应相关。报告了195例不良事件(AE),99例为严重不良事件,96例为非严重不良事件。3例严重不良事件和16例非严重不良事件被认为与伊班膦酸钠治疗有关。3例严重不良事件分别为1例血小板减少、1例恶心和1例发热。

结论

伊班膦酸钠治疗导致血清钙水平呈剂量依赖性降低。对伊班膦酸钠治疗的反应与初始血清钙水平呈负相关,与给药剂量呈正相关。需要2 mg的剂量才能达到与先前使用双膦酸盐帕米膦酸钠和氯膦酸盐的研究相当的反应率。由于药物相关不良事件的发生率较低,可推荐增加伊班膦酸钠剂量用于进一步的临床试验。

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