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撤回:用于转移性骨痛的放射性同位素。

WITHDRAWN: Radioisotopes for metastatic bone pain.

作者信息

Roqué I Figuls Marta, Martinez-Zapata Maria José, Scott-Brown Martin, Alonso-Coello Pablo

机构信息

Iberoamerican Cochrane Centre, Biomedical Research Institute Sant Pau (IIB Sant Pau), CIBER Epidemiología y Salud Pública (CIBERESP), Sant Antoni Maria Claret 171, Edifici Casa de Convalescència, Barcelona, Catalunya, Spain, 08041.

Gray Institute for Radiation Oncology & Biology, Radiobiology Research Institute, Churchill Hospital, Oxford, UK, OX3 7LJ.

出版信息

Cochrane Database Syst Rev. 2017 Mar 23;3(3):CD003347. doi: 10.1002/14651858.CD003347.pub3.

Abstract

BACKGROUND

This is an update of the review published in Issue 4, 2003. Bone metastasis cause severe pain as well as pathological fractures, hypercalcaemia and spinal cord compression. Treatment strategies currently available to relieve pain from bone metastases include analgesia, radiotherapy, surgery, chemotherapy, hormone therapy, radioisotopes and bisphosphonates.

OBJECTIVES

To determine efficacy and safety of radioisotopes in patients with bone metastases to improve metastatic pain, decrease number of complications due to bone metastases and improve patient survival.

SEARCH METHODS

We sought randomised controlled trials (RCTs) in MEDLINE, EMBASE, CENTRAL, and the PaPaS Trials Register up to October 2010.

SELECTION CRITERIA

Studies selected had metastatic bone pain as a major outcome after treatment with a radioisotope, compared with placebo or another radioisotope.

DATA COLLECTION AND ANALYSIS

We assessed the risk of bias of included studies by their sequence generation, allocation concealment, blinding of study participants, researchers and outcome assessors, and incomplete outcome data. Two review authors extracted data. We performed statistical analysis as an "available case" analysis, and calculated global estimates of effect using a random-effects model. We also performed an intention-to-treat (ITT) sensitivity analysis.

MAIN RESULTS

This update includes 15 studies (1146 analyzed participants): four (325 participants) already included and 11 new (821 participants). Only three studies had a low risk of bias. We observed a small benefit of radioisotopes for complete relief (risk ratio (RR) 2.10, 95% CI 1.32 to 3.35; Number needed to treat to benefit (NNT) = 5) and complete/partial relief (RR 1.72, 95% CI 1.13 to 2.63; NNT = 4) in the short and medium term (eight studies, 499 participants). There is no conclusive evidence to demonstrate that radioisotopes modify the use of analgesia with respect to placebo. Leucocytopenia and thrombocytopenia are secondary effects significantly associated with the administration of radioisotopes (RR 5.03; 95% CI 1.35 to 18.70; Number needed to treat to harm (NNH) = 13). Pain flares were not higher in the radioisotopes group (RR 0.74; 95% CI 0.27 to 2.06). There are scarce data of moderate quality when comparing Strontium-89 (Sr) with Samarium-153 (Sm), Rhenium-186 (Re) and Phosphorus-32 (P). We observed no significant differences between treatments. Similarly, we observed no differences when we compared different doses of Sm (0.5 versus 1.0 mCi).

AUTHORS' CONCLUSIONS: This update adds new evidence on efficacy of radioisotopes versus placebo, Sr compared with other radioisotopes, and dose-comparisons of Sm and Re. There is some evidence indicating that radioisotopes may provide complete reduction in pain over one to six months with no increase in analgesic use, but severe adverse effects (leucocytopenia and thrombocytopenia) are frequent.

摘要

背景

这是对2003年第4期发表的综述的更新。骨转移会导致严重疼痛以及病理性骨折、高钙血症和脊髓压迫。目前可用于缓解骨转移疼痛的治疗策略包括镇痛、放疗、手术、化疗、激素治疗、放射性同位素和双膦酸盐。

目的

确定放射性同位素对骨转移患者的疗效和安全性,以改善转移性疼痛、减少骨转移引起的并发症数量并提高患者生存率。

检索方法

我们在截至2010年10月的MEDLINE、EMBASE、CENTRAL和PaPaS试验注册库中检索随机对照试验(RCT)。

选择标准

入选的研究将放射性同位素治疗后的转移性骨痛作为主要结局,并与安慰剂或另一种放射性同位素进行比较。

数据收集与分析

我们通过研究的序列生成、分配隐藏、研究参与者、研究人员和结局评估者的盲法以及不完整的结局数据来评估纳入研究的偏倚风险。两位综述作者提取数据。我们进行了“可用病例”分析的统计分析,并使用随机效应模型计算总体效应估计值。我们还进行了意向性分析(ITT)敏感性分析。

主要结果

本次更新纳入15项研究(1146名分析参与者):4项研究(325名参与者)已纳入,11项新研究(821名参与者)。只有3项研究的偏倚风险较低。我们观察到放射性同位素在短期和中期(8项研究,499名参与者)对完全缓解(风险比(RR)2.10,95%可信区间1.32至3.35;需治疗获益人数(NNT)=5)和完全/部分缓解(RR 1.72,95%可信区间1.13至2.63;NNT = 4)有小的益处。没有确凿证据表明放射性同位素相对于安慰剂会改变镇痛药物的使用。白细胞减少症和血小板减少症是与放射性同位素给药显著相关的次要效应(RR 5.03;95%可信区间1.35至18.70;需治疗造成伤害人数(NNH)=13)。放射性同位素组的疼痛发作并不更高(RR 0.74;95%可信区间0.27至2.06)。在比较锶-89(Sr)与钐-153(Sm)、铼-186(Re)和磷-32(P)时,质量中等的数据很少。我们观察到各治疗组之间无显著差异。同样,在比较不同剂量的Sm(0.5与1.0毫居里)时,我们也未观察到差异。

作者结论

本次更新增加了关于放射性同位素与安慰剂相比的疗效、Sr与其他放射性同位素相比以及Sm和Re的剂量比较的新证据。有一些证据表明,放射性同位素可能在1至6个月内使疼痛完全缓解,且不增加镇痛药物的使用,但严重不良反应(白细胞减少症和血小板减少症)很常见。

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