186Re-1,1-hydroxyethylidene diphosphonate (etidronate) can be used for the palliative treatment of metastatic bone pain. A randomized, placebo-controlled study using 186Re-etidronate was con'/> The Placorhen Study: A Double-Blind, Placebo-Controlled, Randomized Radionuclide Study with 186Re-Etidronate in Hormone-Resistant Prostate Cancer Patients with Painful Bone Metastases
首页> 外文期刊>The Journal of Nuclear Medicine >The Placorhen Study: A Double-Blind, Placebo-Controlled, Randomized Radionuclide Study with 186Re-Etidronate in Hormone-Resistant Prostate Cancer Patients with Painful Bone Metastases
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The Placorhen Study: A Double-Blind, Placebo-Controlled, Randomized Radionuclide Study with 186Re-Etidronate in Hormone-Resistant Prostate Cancer Patients with Painful Bone Metastases

机译:Placorhen研究:186Re-Etidronate与抗激素性前列腺癌痛苦骨转移患者的双盲,安慰剂对照,随机放射性核素研究

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id="p-1">186Re-1,1-hydroxyethylidene diphosphonate (etidronate) can be used for the palliative treatment of metastatic bone pain. A randomized, placebo-controlled study using 186Re-etidronate was conducted on end-stage prostate cancer patients with metastatic bone pain. >Methods: Pain relief was assessed using an electronic diary containing questions reflecting the multidimensional character of chronic pain. The diary was marked twice daily for a maximum of 14 wk (2 wk before and 12 wk after the injection). Pain response was determined using a specific decision rule in which pain intensity, medication index, and daily activities were the core determinants. A positive response day was defined as a day on which pain intensity was reduced a‰¥25% compared with baseline values, while medication index and daily activities were at least constant, or on which pain intensity was reduced 25% and medication index or daily activities improved a‰¥25%, without worsening of the remaining factor. The total response (%) was defined as the number of positive response days divided by the number of days of follow-up. >Results: Of the 111 included patients, 79 were evaluable (43 186Re-etidronate, 36 placebo). Thirty-two patients were excluded from the analysis because of incomplete datasets. The total response of the patients treated with 186Re-etidronate varied from 0% to 96% (mean, 27%, or 23/84 d). In the placebo group, the total response varied from 0% to 80% (mean, 13%, or 11/84 d; Mann-Whitney U test, P 0.05). The number of patients who requested radiotherapy was higher in the placebo group (67%) than in the 186Re-etidronate group (44%) (relative risk, 1.51; Fishera€?s exact test, P = 0.069). >Conclusion: This randomized controlled trial confirmed that, compared with placebo, 186Re-etidronate resulted in a significantly longer pain response in the treatment of bone pain from metastasized prostate cancer.
机译:id =“ p-1”> 186 Re-1,1-羟乙叉基二膦酸酯(依替膦酸酯)可用于姑息性转移性骨痛的治疗。使用 186 Re-etetronate进行的随机安慰剂对照研究是针对患有转移性骨痛的晚期前列腺癌患者。 >方法:使用电子日记评估疼痛缓解程度,其中包含反映慢性疼痛多维特征的问题。每天两次标记日记,最多14周(注射前2周和注射后12周)。使用特定的决策规则确定疼痛反应,其中疼痛强度,用药指数和日常活动是核心决定因素。阳性反应日定义为疼痛强度与基线值相比降低≥25%,而药物指标和日常活动至少保持不变,或疼痛强度降低<25%并且药物指标等于或低于该日。日常活动改善了25%,而其余因素没有恶化。总反应(%)定义为阳性反应天数除以随访天数。 >结果:在111位患者中,有79位是可评估的(43位 186 Re-etidronate,36位安慰剂)。由于数据集不完整,有32名患者被排除在分析之外。用 186 Re-etetronate治疗的患者的总缓解率在0%至96%之间(平均,27%或23/84 d)。在安慰剂组中,总反应从0%到80%不等(平均,13%或11/84 d; Mann-Whitney U 检验, P <0.05 )。安慰剂组(67%)比 186 瑞替膦酸组(44%)需要放疗的患者数量更高(相对危险度为1.51; Fishera精确检验为< em> P = 0.069)。 >结论:这项随机对照试验证实,与安慰剂相比, 186 Re-etidronate在治疗转移性前列腺癌引起的骨痛中导致明显更长的疼痛反应。

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