Loveman Emma, Copley Vicky R, Colquitt Jill L, Scott David A, Clegg Andy J, Jones Jeremy, O'Reilly Katherine M A, Singh Sally, Bausewein Claudia, Wells Athol
Southampton Health Technology Assessments Centre (SHTAC), University of Southampton, Southampton, UK.
BMC Pharmacol Toxicol. 2014 Nov 19;15:63. doi: 10.1186/2050-6511-15-63.
Idiopathic pulmonary fibrosis (IPF) is a life-limiting lung disease with considerable impact on patients and carers as the disease progresses. Currently few treatments are available. We aimed to evaluate the clinical and cost-effectiveness of available treatments for IPF.
Systematic reviews of clinical effectiveness, quality of life and cost effectiveness were undertaken. Eleven bibliographic databases were searched from inception to July 2013 and studies were assessed for eligibility against a set of pre-defined criteria. Two reviewers screened references, extracted data from included studies and appraised their quality. An advisory group was consulted about the choice of interventions. A narrative review was undertaken and where feasible fixed effect and random effects meta-analysis were undertaken including a network meta-analysis (NMA). A decision-analytic Markov model was developed to estimate cost-effectiveness of pharmacological treatments for IPF. Following best practice recommendations, the model perspective was of the national health service and personal social services, a discount rate of 3.5% for costs and health benefits was applied and outcomes were expressed as cost per quality adjusted life-year gained. Parameter values were obtained from the NMA and systematic reviews. Sensitivity analyses were undertaken.
Fourteen studies were included in the review of clinical effectiveness, of which one evaluated azathioprine, three N-acetylcysteine [NAC] (alone or in combination), four pirfenidone, one nintedanib, one sildenafil, one thalidomide, two pulmonary rehabilitation, and one a disease management programme. Study quality was generally good. Evidence suggests that some effective treatments are available. In NMA only nintedanib and pirfenidone show statistically significant improvements. The model results show increased survival for five pharmacological treatments (NAC triple therapy, inhaled NAC, nintedanib, pirfenidone, and sildenafil) compared with best supportive care, at increased cost. Only inhaled NAC was cost-effective at current willingness to pay thresholds but it may not be clinically effective.
Few interventions have any statistically significant effect and the cost-effectiveness of treatments is uncertain. A lack of studies on palliative care approaches was identified and there is a need for further research into pulmonary rehabilitation and thalidomide in particular. A well conducted RCT on inhaled NAC therapy should also be considered.
特发性肺纤维化(IPF)是一种危及生命的肺部疾病,随着疾病进展,对患者及其护理人员有相当大的影响。目前可用的治疗方法很少。我们旨在评估IPF现有治疗方法的临床效果和成本效益。
对临床疗效、生活质量和成本效益进行系统评价。检索了11个文献数据库,时间跨度从建库至2013年7月,并根据一组预先定义的标准对研究进行资格评估。两名评审员筛选参考文献,从纳入研究中提取数据并评估其质量。就干预措施的选择咨询了一个顾问小组。进行了叙述性综述,并在可行的情况下进行了固定效应和随机效应荟萃分析,包括网络荟萃分析(NMA)。开发了一个决策分析马尔可夫模型来估计IPF药物治疗的成本效益。遵循最佳实践建议,模型视角为国家医疗服务体系和个人社会服务体系,成本和健康效益的贴现率为3.5%,结果以每获得一个质量调整生命年的成本表示。参数值来自NMA和系统评价。进行了敏感性分析。
临床疗效综述纳入了14项研究,其中1项评估了硫唑嘌呤,3项评估了N-乙酰半胱氨酸[NAC](单独或联合使用),4项评估了吡非尼酮,1项评估了尼达尼布,1项评估了西地那非,1项评估了沙利度胺,2项评估了肺康复,1项评估了疾病管理计划。研究质量总体良好。有证据表明有一些有效的治疗方法。在NMA中,只有尼达尼布和吡非尼酮显示出统计学上的显著改善。模型结果显示,与最佳支持治疗相比,五种药物治疗(NAC三联疗法、吸入性NAC、尼达尼布、吡非尼酮和西地那非)可提高生存率,但成本增加。只有吸入性NAC在当前支付意愿阈值下具有成本效益,但可能在临床上无效。
很少有干预措施有任何统计学上的显著效果,治疗的成本效益尚不确定。已确定缺乏关于姑息治疗方法的研究,尤其需要对肺康复和沙利度胺进行进一步研究。还应考虑开展一项关于吸入性NAC治疗的高质量随机对照试验。