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大剂量静脉注射帕米膦酸盐治疗转移性骨痛。

High-dose intravenous pamidronate for metastatic bone pain.

作者信息

Purohit O P, Anthony C, Radstone C R, Owen J, Coleman R E

机构信息

YCRC Department of Clinical Oncology, Weston Park Hospital NHS Trust, Sheffield, UK.

出版信息

Br J Cancer. 1994 Sep;70(3):554-8. doi: 10.1038/bjc.1994.344.

Abstract

The bisphosphonates are able to relieve pain from metastatic bone disease and, when given intravenously, may promote bone healing of lytic metastases. In this study, the aim was to assess the acute effects of a single 'high-dose' intravenous treatment with pamidronate on pain, mobility, analgesic consumption and quality of life (QOL). Thirty-four normocalcaemic patients with painful progressing bone metastases (22 from breast, five prostate and seven others) received a single intravenous infusion of 120 mg of pamidronate as palliative therapy. No other systemic therapy or drugs known to influence bone metabolism were administered during the study. Patients' subjective response to treatment was assessed weekly with a pain questionnaire recording a composite of pain intensity, mobility, performance status and analgesic consumption. In addition, patients completed the Rotterdam Symptom Check List (RSCL) for measurement of QOL and a mobility questionnaire. The mean reduction in the pain questionnaire score (recorded on at least two occasions) was 25% [standard error (s.e.) 3%, range 0-75%]. Twenty patients (59%) showed a > or = 20% improvement and were classified as responders. The median duration of symptomatic response was 12 (range 4-24 +) weeks. The responding patients showed a reduction in RSCL score (improvement in QOL) from 35% before treatment to 27% at 6 weeks, but no significant improvement was noted in non-responders. Twenty-one patients were retreated with pamidronate when their symptoms deteriorated again. Eight out of 15 responders showed a second reduction in pain score of > or = 20%, but this was not seen in any of the six non-responders. Five patients have remained well with no additional treatment for their disease other than repeat infusions of pamidronate every 3-6 months. Treatment was well tolerated. Eight (24%) experienced fever after the first treatment only, and four had asymptomatic, biochemical evidence of hypocalcaemia. The acute inhibition of osteoclastic bone resorption induced by a single high-dose treatment with pamidronate can provide useful palliation for patients with bone metastases. Responding patients may be retreated as symptoms dictate to good effect. We are currently running a phase III double-blind trial with high-dose pamidronate for progressive painful metastatic bone disease to exclude any placebo effect and observer bias.

摘要

双膦酸盐能够缓解转移性骨病引起的疼痛,静脉给药时,还可能促进溶骨性转移灶的骨愈合。本研究旨在评估静脉单次“高剂量”使用帕米膦酸对疼痛、活动能力、镇痛药用量及生活质量(QOL)的急性影响。34例血钙正常、有进展性疼痛性骨转移的患者(22例来自乳腺癌,5例来自前列腺癌,7例来自其他癌症)接受了120mg帕米膦酸的单次静脉输注作为姑息治疗。研究期间未给予其他全身治疗或已知会影响骨代谢的药物。每周用疼痛问卷评估患者对治疗的主观反应,该问卷记录疼痛强度、活动能力、身体状况及镇痛药用量的综合情况。此外,患者完成鹿特丹症状检查表(RSCL)以评估生活质量,并完成一份活动能力问卷。疼痛问卷评分(至少记录两次)的平均降低幅度为25%[标准误(s.e.)3%,范围0 - 75%]。20例患者(59%)改善幅度≥20%,被归类为反应者。症状缓解的中位持续时间为12周(范围4 - 24 +周)。有反应的患者RSCL评分降低(生活质量改善),从治疗前的35%降至6周时的27%,但无反应者未观察到显著改善。21例患者症状再次恶化时再次接受帕米膦酸治疗。15例有反应的患者中有8例疼痛评分再次降低≥20%,但6例无反应者均未出现这种情况。5例患者病情稳定,除每3 - 6个月重复输注帕米膦酸外未接受其他疾病治疗。治疗耐受性良好。8例(24%)仅在首次治疗后出现发热,4例有无症状性低钙血症的生化证据。单次高剂量使用帕米膦酸诱导的破骨细胞骨吸收急性抑制可为骨转移患者提供有效的姑息治疗。有反应的患者可根据症状决定再次治疗,效果良好。我们目前正在进行一项关于高剂量帕米膦酸治疗进展性疼痛性转移性骨病的III期双盲试验,以排除任何安慰剂效应和观察者偏倚。

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